Interactive Transcript
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hundreds of case-based microlearning courses across all key radiology
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subspecialties. Today we are honored to welcome Dr.
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Erin Gomez for a lecture on complex and high risk OB pathology.
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Multimodal case review. Dr.
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Erin Gomez completed her diagnostic radiology residency in body r i
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subspecialty training at the Johns Hopkins Hospital in Baltimore, Maryland.
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She's an assistant professor in the diagnostic imaging division at Johns Hopkins
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where she specializes in cross-sectional imaging of the female pelvis and
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medical school students and resident education. At the end of the lecture,
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please join Dr.
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Gomez in a q and a session where she will address questions you may have on
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today's topic.
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Please remember to use the q and a feature to submit your questions so we can
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get to as many as we can before our time is up. With that,
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we are ready to begin today's lecture. Dr. Gomez, please take it from here.
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Alright, awesome. Hi everyone, I'm Erin Gomez. Um,
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I'm a radiologist at Johns Hopkins in Baltimore, Maryland.
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And today I'm thrilled to take you through a multimodal high-risk
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OB pore case review.
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In today's conference we'll talk about the normal imaging appearance of the
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uterus and ovaries in pregnant and non-pregnant patients and expected changes
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during pregnancy. I'll also tell you about indications for ultrasound,
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CT and M R I during pregnancy and then we'll talk about key imaging features of
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acute abdominal pelvic pathology during pregnancy, ectopic pregnancy,
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gestational trophoblastic disease,
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and other risk high and other high risk OB partum processes.
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Um, the gestational trophoblastic disease cases.
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That'll show today our courtesy of my colleague Dr.
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Jamie Marco and the A I R P archives and I'd like to thank him for sharing those
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with me for today. Let's get started.
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Let's talk about what you should expect to see when you're looking at the uterus
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and ovaries on cross-sectional imaging pelvis.
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So this is a statute teaching weight I of the pelvis.
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You can see that the uterus is here.
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It's a pear shaped organ and it's interposed between the bladder,
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which is here anteriorly and the rectum, which is here posteriorly.
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The ovaries are often lateral to the uterus.
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So this is the right ovary on this axial T2 weight image of the pelvis.
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And this is the left ovary and it's easy to find the ovaries because you'll
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often see them along the course of the external iliac vessels.
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And on T2 weed imaging of the pelvis they'll have T2 hyperintense follicles.
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Let's take a more detailed look at the anatomy of the uterus and
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ovaries and some of the ligaments that we can see in the pelvis,
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specifically on r i. Um, so let's talk about the parts of the uterus.
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First of all, the uterus can be separated into the fundus,
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which is the superior most portion of the uterus and then the uterine body.
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The term lower uterine segment is reserved for the context of pregnancy and it's
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not something that we normally describe in non-pregnant patients.
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This is the cerv on the ULT two weighted M R F, the pelvis.
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This is the anterior lip of the cervix, posterior lip of the cervix.
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And this is the cervical canal on M R I. We can also see the vagina.
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And again, as I mentioned,
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these are the ovaries looking more closely at the distinct layers
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of the uterus, we can see the endometrium here centrally. It's T2 bright,
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this is the junctional zone.
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It's this dark band of tissue beyond the endometrium.
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And the reason the junctional zone looks dark is it is also myometrial tissue
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similar to this layer out here, but it's more densely packed.
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Those myocytes are closer together so they have a lower water content, um,
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and they won't look as bright on T2 rated imaging as the myometrium proper,
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which is out here.
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And then finally this thin black line that covers the uterus is the uterine
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serosa.
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Other structures that I'd like to point out on this POAL T2 rated image,
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we can see the broad ligaments at these arrows and then the round ligaments at
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the portfolio arrows.
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So lots of changes happen to the uterus during pregnancy.
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The uterus increases in size a lot and there is predictable growth here, right?
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That's why we measure patients' bundle height.
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When they come in for OB imaging or OB appointments,
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the pregnancy is supported by the corpus lutetium until about 10 to 12
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weeks gestation. And then the placenta takes over.
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And so as the uterus ascends into the abdomen as it grows the abdominal viscera,
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the ovaries and the bowel all get displaced laterally.
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You also have an increase of blood volume and proliferation of the pelvic blood
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vessels.
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Now we're gonna talk a lot about CT and M R I today,
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um, because many of the complex and high-risk OB cases that we encounter
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end up requiring more advanced cross-sectional imaging of the abdomen and
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pelvic.
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But far and away ultrasound is the first line imaging modality in pregnancy,
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right? And that's for many good reasons. It's readily available,
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there's no ionizing radiation employed.
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We can get really beautiful high resolution images of the uterus and the ovaries
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on both TA and Transvaal imaging.
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And it is definitely our go-to for evaluating first trimester pregnancy, um,
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most commonly viability, but also pregnancy related complications.
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This is a 3D reconstruction of a transvaginal ultrasound for a patient with
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a first trimester pregnancy. We can see the amniotic stack here.
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We can see the embryo and an adjacent.
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Let's talk about mri cause many of the cases we'll see today are MR based
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MRI is considered very safe during pregnancy.
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There's no ionizing radiation employed.
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And so it's a great imaging technique for patients who are pregnant.
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We can get large field of view imaging with excellent tissue characterization
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and that's because we can weight the images as we desire. Um,
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but also the resolution is really beautiful.
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The other good thing about MRI is it's often diagnostic without IV contrast.
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So we don't have to administer gadolinium based contrast agents or GCs to
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pregnant patients, which is um, a practice that is, um,
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largely frowned upon as gadolinium based contrast. Agents cross the placenta,
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they cross the placenta, enter the fetal circulation.
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We know that gadolinium as a contrast agent is excreted renally.
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And so because it enters the fetal circulation is excreted into the amniotic
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fluid, um, by the fetus ingested again and excreted again.
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And so it takes much longer to clear gadolinium based contrast from the fetal
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circulation than it does the maternal circulation.
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And there are some studies that suggest that there's a higher risk of
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inflammatory and skin and rheumatologic conditions in fetuses who have been
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exposed to gag.
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There's also emerging data about gadolinium deposition within tissues in the
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body, including the basal ganga. And so for all those reasons,
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we do not give gaag to pregnant patients unless there's a situation, um,
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that really necessitates it. Um,
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like a patient who's had a fetal demise but has an abnormal placenta that
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requires operative cleaning.
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Another thing that I'd like to point out is that MRI can be performed in
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pregnant patients at both 1.5 and three Tesla.
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There used to be concerns about tissue heating and specific absorption rate,
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but we know now that really most of the heat that's generated during an M R I is
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actually deposited at the skin surface, which is maternal.
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Any heat that does reach the fetus is dissipated by circulation of the amniotic
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fluid. So pregnant patients can be imaged at 1.5 or threet.
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And then there is a theoretical risk to the fetal obstacles due to noise that
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happens during the exam, particularly during gradient echo imaging.
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But none of that has ever panned out in human studies.
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So suffice it to say that MRI is very safe during pregnancy.
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Let's get right into it. Now let's talk about some pathology.
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This is our general abdominal protocol. Um,
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for pregnant patients, uh,
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it's basically the same as our general admin protocol I,
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except we've omitted the post contrast images. We start with a scalp.
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We do axial and coronal T2 weight images in phase and out phase imaging.
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We do diffusion with a corresponding ADC map.
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We do a pre contrast axial T1 and then if the patient is having an
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R C P will also add coronal single shot T2 related images.
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Now this is a list of many potential causes of abdominal pelvic pathology
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during pregnancy, but it's not exhaustive, right?
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There are other things that could happen beyond this list and we're not even
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going to discuss all of them today.
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But I just wanna give you an idea for sort of the broad categories and many
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different things that can result in abdominal pelvic pain in a pregnant patient
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and they can be classified into GI gu.
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The top two causes of abdominal pain in pregnancy are acute appendicitis and
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obstructing nephro ral stone,
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but obstetric and gynecologic conditions can also um,
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alert patients to the attention of providers and prompt further imaging.
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So let's just do a sampling of cases related to a few of these different
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conditions.
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So I'll start with um, these three images.
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This is a patient who presenting with right upper quadrant pain at 26 weeks
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gestation.
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She has a history of hepatitis C and we have axial T2 weighted
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images here on the left side of the screen and then a coronal Mr C P image on
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the right side of the screen.
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And I'll give you just a minute to take a look at it and see what you think
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about these before I discuss the findings.
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And we can see a little bit of the fetus here in the grab ute on the mrp.
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This is blood Blood. Okay,
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so one of the first things I wanna point out on this T2 rated image is all of
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this edema and T2 right signal around the portal vein.
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This patient has periportal edema. Additionally,
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the gall bladder looks really thick but there's not a ton of per
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cystic fluid.
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And on the RCP image there is no intra hepatic ary ductile dilation.
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So when we interviewed this patient further, she had had flu life symptoms, um,
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for about a week prior to coming in and she had been taking a lot of Tylenol.
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So given her background liver disease, um,
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this was a patient who had acute hepatitis due to an accidental Tylenol
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overdose. And so, um, the periportal edema is a classic finding in hepatitis.
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And all of this thickening and emus changes within the wall of the gallbladder
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is reactive in the setting of adjacent liver inflammation.
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Next case is a pregnant patient at 13 weeks gestation presenting with left
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inguinal pain. And so we have two coronal stir images.
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Um, of the pelvis here is the Ravi uterus. This is patient right,
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this is patient left.
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You can see a little bit of the urinary bladder and pubic synthesis here.
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Same thing on these images. We catch a little bit of the cervix,
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which is here and the gravity uterus.
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And so this patient is coming in with left inguinal pain.
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So I'll direct your attention to this area of the image.
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And this is a little bit of an eye test for symmetry,
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but if you notice that the um,
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left femoral iliac vessel when compared with the right, they're really engorged.
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They're very dilated.
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There is a T2 hyperintense filling defect within the left
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femoral iliac Venus system.
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We can see it extending up into the left common iliac vein.
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There's a bunch of surrounding edema, these tissues here in the retro peroneum,
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also low emus.
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And so this is a patient who has an extensive left immoral D V T
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companion case to go along with that one. This patient um,
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presented with ovarian vein thrombosis and the postpartum period.
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So she was 41, she just had a C-section. Um,
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and she'd had a bunch of complications but she was having pretty dramatic pelvic
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pain. And so we did a CT for this patient.
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We can see the enlarged postpartum uterus here.
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Then there's really marked thickening of the right gonadal vein.
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We can see that it's expanded by this hyperdense thrombus that extends all the
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way up into the I V C.
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So this is another vascular complication that can occur not only in the context
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of pregnancy but in the postpartum period.
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Particular cation has had cesarean section.
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We'll switch gears a little bit.
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This is truly a potpourri of cases that are causing pain, um,
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in pregnant patients. So this is a patient who is 22 weeks pregnant.
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She was coming in with a little bit of pelvic discomfort and on her pelvic
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ultrasound she had a complex NAL lesion.
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So I'll give you a moment to look at these images.
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This is an axial T2 weighted image of the pelvis. And then we have t1,
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non-fat saturated and fat saturated images here on the top and bottom
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respectively.
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So one of the first things that we see for this patient is she has this big
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cystic lesion posterior to the uterus. It has some thin little ations within it.
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And then there is this nodular component along the right lateral aspect.
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When we look at the non-fat saturated and fat saturated images,
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this ated component seems to have something different within it,
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but it's unchanged between the uh, non-fat, fat and fat saturated.
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But this tiny little nodule does seem to drop out on the fat saturated
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in images.
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And so this patient went for surgery while she was pregnant to have this
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removed and this ended up being uh,
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a combination lesion of a mature cystic keratoma and a mucinous cystadenoma.
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And I think we can see features of both here, right?
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We have this large cystic lesion with a fatty neural nodule but also
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citations within a predominantly cystic lesion,
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which seem to have maybe some slightly more complex material within them.
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This is another patient who um,
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is having pain who was admitted to the hospital with preeclampsia and is now
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got his post cesarean section. She's also in renal failure,
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which is the reason for us doing this non-contrast CT of the pelvis
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and sorry, chest, abdomen, and pelvis. Um,
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she's also having a drop in hemoglobin.
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And so we have stagial and axial non-contrast
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CT images of the abdomen.
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We also have a lung window image at the level of the lung basis.
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On the sagittal image we can see the enlarged um, postpartum uterus.
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You can see a little bit of tissue edema here in the lower uterine body, right?
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It's no longer the lower uterine segment because the patient is no longer
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pregnant. So we teach,
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we see tissue edema at the site where they made the incision for the caesarean
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section. And we also see an appropriate amount of gas, um,
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surrounding the uterus. And in the lower pelvis, this is all post-surgical gas.
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I'll now dry your attention to the axial non-contrast CT image in the center
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of the screen. And so again, we see an enlarged postpartum uterus.
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We see a little bit of postoperative hemoperitoneum and probably hemoperitoneum.
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But then in the left anterior abdominal wall we see a fluid collection which is
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demonstrating what's called hemato effect, right?
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So we have hypodense material within the, um,
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anterior aspect of this collection and then hyperdense material and the
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dependent portion of it.
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And so what this is is blood products that have separated out.
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And so the more dense heme has settled to the bottom and then the plasma is left
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at the top. And so this patient has a big anterior abdominal wall hematoma.
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She also has at least small but probably moderate bilateral pleural
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effusions, um, and a little bit of ground glass at both lung bases.
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So she probably has a little bit of pulmonary edema as well.
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So all of these things put together, um,
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this patient who had preeclampsia is now having evidence of um,
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greater than expected postoperative bleeding.
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She's having end organ complications and also pulmonary edema.
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This is a case of help syndrome. Help syndrome stands for hemolysis,
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elevated liver enzymes and low platelets, right?
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So this is a form of preeclampsia.
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It is severe and it is life-threatening cause these patients bleed and they have
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hepatic complications. Most commonly. This patient fortunately did not.
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Um,
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so common complications related to the liver include subcapsular hematoma,
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peri hepatic bleeding, hepatic rupture. Um,
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but you can also see just in general bleeding di cause these patients
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often go on to develop D I c, um,
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which is both a disorder of clotting and bleeding.
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And so I suspect that this patient's abdominal hematoma is related to, um,
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the D I C as a result of her health syndrome. Um,
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the treatment for these patients is largely supportive. Um, they will manage,
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um,
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laboratory abnormalities and support the patients until organ function recovers.
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And then of course anything that's actively bleeding that could be embolized or
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managed by interventional radiology as taken care of as well.
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This is sort of a companion case.
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Now this is a patient who is at 37 weeks gestation.
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She came in with right shoulder pain that was radiating all the way down to her
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right point and um,
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she had a CT of the abdomen and pelvis.
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They suspected that she was having some kind of gallbladder pathology or maybe
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even had a renal stone. Um,
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but her pain was so severe that they ended up doing a ct.
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And so we'll draw your attention to the right adrenal gland.
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Here's the left adrenal gland hiding out on this coronal uh, CT image.
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The right adrenal gland is expanded.
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We really can't even differentiate the limbs.
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It's hyperdense and appearance centrally.
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There's a bunch of fat stranding around it.
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You can see some riskiness of the fat here. Here it is again on the sagittal,
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um, post contrast image of the ct.
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And so this patient has a spontaneous adrenal hemorrhage. Um,
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these can happen for a variety of reasons. One of the things to know about,
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um, adrenal hemorrhages is that one is okay, right?
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It's not ideal. It can be painful.
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It's often in the setting of some other systemic abnormality or acute stress.
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But one adrenal gland hemorrhage is all right.
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If a patient has bilateral adrenal gland hemorrhage,
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especially in the context of pregnancy, is this something that's dangerous?
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Because if both of your adrenal glands are hemorrhaging and are not functioning
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properly, it places the patient at risk of severe adrenal insufficiency.
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And so those patients have to be monitored in the icu. Um,
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but this patient was okay. Um,
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on these images we can also see right hydronephrosis of pregnancy.
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This is the common finding of pregnant patient due to compression of the ureter.
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Um,
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this patient came back about a year later and this right hemorrhage had resolved
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and there was no mass or or nodule that was underlined.
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Let's wrap up this section of acute abdominal path. Uh,
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acute abdominal pelvic pathology during pregnancy.
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Clinical history and symptoms will often guide the initial imaging because it'll
20:25
help you pick from one of those five or six categories that we briefly talked
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about. Ultrasound is first line imaging for evaluating uterus, ovaries,
20:33
and fetus.
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You can use CT if you need to in patients with severe or acute symptoms.
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An MRI can be a really helpful adjunct imaging modality in characterizing
20:42
findings that you first see on ultrasound or for troubleshooting lesions or
20:47
pathology that you find. Next.
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Let's move on to talk about advanced or complex ectopic pregnancy.
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So you've all probably seen ultrasound images of an atopic pregnancy, right?
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And this is atopic pregnancy refers to implantation of a fertilized o outside
21:06
the endometrial cavity.
21:08
The most plastic location is the pul of the fallopian two, right?
21:12
And that's where you're gonna see and in exel mass and on ultrasound,
21:16
you're gonna see what the ring of fire.
21:18
It's gonna be a ring-like hypervascular structure.
21:21
And that's true for all imaging modality no matter what you're using to image,
21:26
uh, and all. And atopic pregnancy will look like a hypervascular ring.
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Another finding that can guide you toward atopic pregnancy
21:36
of the diagnosis is absence of an intrauterine gestation or an abnormal or
21:40
inappropriate rise in beta H C G, right? Especially in the first time trimester.
21:44
We expect the beta HCG to double every 48 to 72 hours.
21:50
Atopic pregnancy is dangerous.
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These patients have the potential to severely hemorrhage if the atopic pregnancy
21:56
ruptures.
21:57
And so that's why imaging is super important in identifying the condition.
22:02
More severe or rare manifestations of atopic pregnancy can also be
22:07
really well-characterized by mri.
22:09
And so that includes things like cervical and cesarean section, scar,
22:12
atopic pregnancy.
22:16
Let's start with a quote, easy case. Um,
22:19
so this is a ruptured ectopic and I wanna clean out the features here, um,
22:24
that really highlight how dangerous this condition is.
22:27
So this is a patient who was 43.
22:29
She came into the emergency room with decreased responsiveness and she was
22:33
hypotensive and they did a fast exam right where they looked at all of the
22:37
different abdominal quads within ultrasound and they saw chemo,
22:41
peritoneum and fluid in the abdomen and pelvis.
22:45
And so this patient was not doing well.
22:47
There was no time to perform an ultrasound for this patient.
22:50
She went straight to the CT scanner and here's what we saw.
22:54
So we did arterial and venous phase and it is of the abdomen and pelvis.
22:58
Down here in the pelvis we can see that there is an ovoid
23:03
structure. It has some vascularity around it, even on the arterial phase.
23:08
On the venous phase. This fills in as a hypervascular ring.
23:13
Um,
23:14
and then the way that we can prove for ourselves that this is actually an ect,
23:18
capd pregnancy is number one. This is the uterus, right? We can see it here.
23:22
We can see it here.
23:23
This structure is independent from the uterus and we are so fortunate to have a
23:28
purpose rium in the right ovary adjacent to the uterus.
23:32
So this is independent of the ovary, independent of the uterus.
23:35
It's a hypervascular ring in the right aa and there is a ton of abdominal
23:40
pelvic hemoperitoneum up here near the dom of the liver here surrounding the
23:44
spleen. Um,
23:45
along the right peric collic gutter and then down here in the pelvis.
23:49
And so this is a ruptured ectopic pregnancy until proven otherwise.
23:53
This patient was taken emergently to the operating room.
23:55
She had a laparoscopic self ectomy and um,
23:58
they confirmed a diagnosis of ruptured right tubal atopic pregnancy.
24:04
Now let's do a more complex case.
24:07
The 25 year old presenting with right sided pelvic pain.
24:11
Her last menstrual period was seven weeks ago.
24:15
She had an ultrasound which was abnormal and MRI was performed for further
24:20
characterization.
24:22
So we have an axial T2 fat saturated image of the pelvis.
24:26
You have a sagittal T2 weighted image of the pelvis and a coronal T2 weighted
24:30
image of the pelvis.
24:32
And so what I'd like to point out here are those layers of the uterus that we
24:37
looked at on those normal images first, right?
24:38
So this is T2 hyperintense and heterogeneous myometrium out here.
24:44
This is the junctional zone.
24:45
And then you see the endometrium here and within the endometrial cavity toward
24:50
the right side of the uterus heading toward that OAM where the fallopian tube
24:55
enters, we again see a cystic rin leg structure.
24:59
It's really well circumscribed,
25:01
it's thick walled and it seems to be heading out toward again the uterine corn.
25:08
And so this patient has an interstitial atopic pregnancy. Um, this is technic,
25:12
some people will use the term corn corneal atopic pregnancy interchangeably with
25:17
interstitial atopic, but they're not the same thing. Corneal atopic corn.
25:22
Corneal pregnancy refers to a pregnancy which occurs within
25:26
one formula of a bi cornal uterus.
25:29
And so interstitial atopic pregnancy really hones down more, right?
25:33
It is within the periphery of the uterus, the interstitial, um,
25:37
where the fallopian tube meets the uterus.
25:42
And so this is probably an atopic pregnancy that was on its way to becoming
25:46
tubal, but never made it there.
25:48
Interstitial atopic pregnancy is extremely dangerous.
25:51
The interstitial of the uterus,
25:53
this sort of corner or lateral super lateral aspect of the uterus is extremely
25:57
hypervascular.
25:59
And so these patients are at risk for catastrophic hemorrhage if this atopic
26:03
pregnancy measures. Here's another case.
26:07
This is a patient who again had an abnormal ultrasound in the context of
26:12
pregnancy. Um, she had a history of heavy vaginal bleeding,
26:15
but it had significantly increased within recent weeks.
26:19
And so we have sagittal coronal and axial T2 rated MR images of the pelvis.
26:24
You can see the uterus here, right?
26:25
It's fairly enlarged and she has a bunch of T2 hyperintense uterine masses.
26:30
These are fibroids and probably account for her lung history of heavy vaginal
26:35
bleeding. But I'd like to draw your attention here to the cervix.
26:40
Okay, so this is anterior lip of the cervix, posterior lip of the cervix.
26:44
Within the cervix we can see an expanded tissue mass.
26:48
It's heterogeneous, it's T2 bright.
26:52
When we look at the coronal and axial images,
26:55
we can see that the cervix is really thickened. It's very hetero heterogeneous.
26:59
We see a bunch of serpiginous, linear T2, hypo intense structures.
27:04
These are flow voids in the context of abnormal and proliferative cervical
27:09
vascularity. And then within the center here we see a cystic lesion.
27:13
This is the gestational sac. Okay? So this is t2, bright gestational sac,
27:18
and within it we can actually see a fetal pole.
27:22
And so this is a pregnancy that's centered within the cervix.
27:25
This is a cervical ectopic pregnancy. Again,
27:28
it's extremely important to manage these patients either with embolization or
27:32
methotrexate and or surgical treatment because there's a risk of catastrophic
27:36
hemorrhage of disrupt.
27:41
Next I'd like to show a case from my high risk OB mastery series with
27:46
modality. Um, this is a patient who has a known ectopic pregnancy, which was,
27:50
and she was last to follow up. Um,
27:53
she initially presented with an ectopic around seven week shift station.
27:57
She was offered medical management for it and she declined.
28:01
And then we did not see her again until she was about 26 weeks pregnant and
28:06
came back with imaging that looked like this. So lemme orient you a bit.
28:11
First, this is the patient. Uh, this is the patient on Corona T2 weight images.
28:15
And then this is an axial T2 weight image of the abdomen and pelvis.
28:19
And so let's identify all of the structures that are present here.
28:22
This is the uterus and we can again, see those distinct layers. Right?
28:26
Here's t2, bright endometrium. This is junctional zone. This is t2,
28:31
heterogeneous myometrium. And then t2, dark ci rosa. This thin black line,
28:36
this is the patient's placenta and it's very abnormal.
28:40
Normally the placenta should be uniform in its signal and thickness.
28:44
This patient has big placenta bands, um,
28:47
which are a feature of abnormal place presentation.
28:50
And then in the center of the images,
28:52
independent from both the uterus and the placenta is the fetus.
28:57
And so again, let's just point out uterus, fetus, placenta, uterus,
29:02
fetus, placenta.
29:03
And so this is a patient who has an intraabdominal atopic pregnancy.
29:07
This happens when the pregnancy implants in the abdominal cavity instead of
29:12
uterus. And um,
29:13
we can really develop in a number of different ways the pregnancy implant on the
29:18
utero, mentum on large vessels, on vital organs.
29:22
And these patients can also bleed to death if this goes undetected until late in
29:26
the pregnancy.
29:28
We use r i primarily for operative planning to locate the placenta and to see
29:32
which organs, if any, have been invaded. Um, and this patient had, um,
29:37
exploratory laparotomy at 28 weeks gestation and both mother and fetus survived.
29:44
Let's move away from ectopic pregnancy and explore some other high risk OB
29:49
topics. I'll start with a case of placental abruption.
29:53
And this is something that you may see in your practice and you may have already
29:56
seen.
29:57
And it's important to know the imaging feature cause you could save somebody's
30:00
life if you're able to recognize this. This is a 29 year old woman,
30:04
she's 38 weeks pregnant. She was in a motor vehicle collision.
30:08
She had a positive seatbelt sign, lots of abdominal pain on physical exam.
30:12
And she had a non-reassuring fetal heart rate on the tracing.
30:16
So we put her in the CT scanner, we gave contrast, right? If you're gonna do it,
30:20
do it right. And so, um, we have contrast enhanced ct.
30:24
Here are the abdomen published. These are axial images.
30:27
This is a corona and this is a sagittal image.
30:29
And so we see the Ravi uterus here, right? We see fetal parts.
30:32
This is fetal abdomen, fetal limbs. And then this is the placenta.
30:37
Now this placenta, I can tell you may not have seen a lot of placenta on ct,
30:41
but they should be bright if you're giving contrast cause they're highly
30:44
vascular and so they should be enhancing.
30:47
And so the features I wanna point out about this placenta is that it's really
30:50
heterogeneous.
30:52
There are only a few areas where there's normal appearing enhancement.
30:57
We see these big global patchy areas of pipeline enhancement within the
31:01
placenta.
31:03
Less than 50% of the placental parenchyma is demonstrating normal enhancement.
31:08
And so this is highly concerning for placental abruption.
31:11
If you scan a pregnant patient with contrast and the placenta is not enhancing
31:15
normally and they are having abdominal pain,
31:18
this is placental abruption until proven otherwise,
31:20
this patient went for emergency section, the fetus survived,
31:24
the mother survived, and a diagnosis of placental abruption was confirmed.
31:31
Here's another case.
31:33
This is a patient who had pelvic pain and when she went for her OB ultrasound
31:38
with maternal fetal medicine,
31:39
we were having a really challenging time seeing her cervix.
31:44
And so we have statutal tissue,
31:46
tissue weed image of the pelvis here and a coronal de two weight image of the
31:49
pelvis year. The patient is status kidney transplant.
31:53
And so that's what you're seeing here in the right lower quadrant.
31:56
Now I'd like to point out on the coronal image that we can see our t2,
32:00
heterogeneous my nutrient. We see the, uh,
32:03
gestational sac or the amniotic sac here with theus inside.
32:07
And then this is the urinary bladder and this is the cervical canal.
32:12
Now I challenge you to find the cervical canal on the sagittal image.
32:17
So we see this big bulge, this is the lower uterine segment here.
32:21
And then to orient you, this is the uterine fundus.
32:25
And if we follow from the vagina all the way up, this is actually the surface.
32:30
It's very elongated, it's very compressed,
32:33
it's anterior and location and is being pushed forward by the fundus of
32:38
the uterus, which is doubled back here and is resting in front of the safe belt.
32:44
So this is a case of uterine incarceration.
32:48
Uterine incarceration is defined as entrapment of a retroverted uterus in the
32:51
pelvis. It's fairly rare,
32:53
one in 3000 pregnancies and it often happens in the second trimester.
32:58
And so what'll happen is these patients will come into the office,
33:00
the bundle height on physical exam is discordant with their dates.
33:04
And then when they try to see the cervix on ultrasound, um,
33:07
it's either significantly displaced or is anteriorly located.
33:12
There are lots of different ways to try to resolve this.
33:14
They can do version maneuvers, um,
33:17
which is just physically pressing on the uterus to try to relocate it.
33:21
Sometimes this has to be done under anesthesia. Um,
33:25
and then complications of this, because the uterus is so abnormally positioned,
33:30
um, the patients are at risk of uterine rupture, right?
33:32
There's already a little bit of sort of thinning and expansion of the lower
33:36
uterine segment here or bladder ruptured due to mass effect.
33:40
This is the same patient.
33:42
Two weeks later she came in with abrupt onset abdominal pain. She had,
33:47
um, been planned to come into the office for a, uh,
33:51
version maneuver to correct the position of her uterus.
33:54
And so now on the statute teaching weighted image,
33:57
we see that the cervix is in a much more normal location and the fundus of the
34:01
uterus is now in the abdomen instead of in front of the sac inflammatory.
34:05
So the reason that this patient came in with abdominal pain is because her
34:09
uterine incarceration spontaneously resolved.
34:15
Next case,
34:16
this patient with persistent reading following a spontaneous abortion during
34:20
that pregnancy,
34:21
the patient's medical imaging had suggested a diagnosis of placenta accreta
34:26
spectrum. Now again,
34:27
placenta accreta spectrum is a range of conditions in which the placenta is
34:31
morbidly adherent to the uterus or the myometrium,
34:34
the muscular layer of the uterus. And so these patients,
34:37
if they have a spontaneous vaginal delivery, are at increased risk of bleeding,
34:41
um, because the placenta may not completely detach from the uterus.
34:46
So we have two ultrasound images of the pelvis for this patient.
34:50
We're at the level of the mid uterus and we can see that the endometrial cavity
34:54
is distended. It's some sort of heterogeneously hypoechoic material.
34:58
These are endo vaginal images. And when we come up a little bit closer,
35:02
you can see that this material is fairly vascular.
35:06
An MRI was performed for further characterization.
35:09
And so this patient, um,
35:12
this is a sagittal T2 weighted image of the pelvis.
35:15
You can see the urinary bladder here. This is the vagina and this is the uterus.
35:19
You can see that it's enlarged. Um, and is, uh, you know, um,
35:24
postpartum uterus, the patient has, um,
35:26
passed the fetal parts and the endometrial cavity is distended.
35:31
Um, it isn't that typical T2 hyperintense appearance that we expect to see.
35:36
There's probably, probably a little bit of heterogeneous material in here.
35:39
And then in the low anterior uterine body, there's this T2 bright lesion,
35:44
which seems to extend into the my,
35:47
this is a T1 pre contrast image where that, uh,
35:51
focus looks fairly homogeneous in terms of its relationship
35:56
to the rest of the uterus. And then in both contrast images,
36:00
this appears to invaginate into the my and demonstrates some enhancement
36:05
of its own. And so this is retained placenta.
36:08
It's can be more broadly classified as retained products of conception.
36:13
Retained POC is persistent placental or fetal tissue in the uterus after a
36:18
delivery of miscarriage or a termination of pregnancy.
36:21
What it's gonna look like is a soft tissue lesion within the endometrial cavity.
36:24
And it's gonna look like that on all of the different imaging modalities we
36:28
perform. The vascularity is can confirmatory of this condition,
36:31
but it can vary a lot.
36:33
One of the things that can first clue you in to retained product is an
36:38
endometrial thickness of greater than or equal to 10 millimeters following a
36:41
spontaneous abortion or a dilation of.
36:45
Now one pearl that I wanna point out to you is if we had been looking at these
36:50
ultrasound images and the patient was actively passing clots was still feeling
36:55
heavy abdominal clamping, um, you know,
36:57
and and had an appropriately following H C g hadn't had any imaging suggestive
37:02
of placenta accreta spectrum.
37:04
We say that the patient has an abortion in progress and it's a pitfall to make a
37:08
diagnosis of routine products while the patient is actively miscarrying.
37:12
Do you have to use the clinical history to guide your interpretation of these
37:15
images? Next case,
37:19
this is a patient with abdominal cramping.
37:22
She has a history of prior cesarean section.
37:25
She had an abnormal ultrasound with maternal fetal medicine.
37:28
This a stage T2 weighted image of the pelvis.
37:32
You can see the placenta here anteriorly. It's really lovely. Um,
37:36
it's very homogeneous, uh,
37:38
on these images and it has a little bit of peripheral tapering,
37:41
which is angular. So the majority of this placenta is very normal.
37:45
You can see t2, heterogeneous myometrium covering it.
37:48
There's a little bit of increased sub placental vascularity.
37:52
The penis is in a transverse position here, right? It's here had is here.
37:57
What I'd like to point out for this patient is this really dumbbell shaped
38:00
appearance of the amniotic sac. And we can see that on the coronal as well.
38:05
If we follow the my down. It gets very,
38:08
very thin here and it looks like the lower uterine segment is almost
38:13
being buttressed or supported by the dome of the urinary bladder.
38:18
If you measure this, the myometrium gets as thin as one to two millimeters here.
38:22
And then the bladder dome, you know,
38:25
combined this measurement is probably five to six milliliters.
38:29
There is one area of the placenta in on the left side that does look
38:34
abnormal is heterogeneous.
38:35
And this patient probably has a little bit of focal placenta of RTA here as
38:39
well. But let's focus on the imaging findings here.
38:42
These imaging findings raise concern for uterine des.
38:46
Now I wanna make it clear that you can't call uterine des unless you have
38:51
complete separation of the endometrium and myometrium. So for this patient,
38:55
we still see a thin, thin,
38:57
thin layer of myometrium measuring two millimeters here. Um,
39:02
this is distinct from a uterine rupture,
39:04
which includes separation of the serosa in the postpartum period.
39:09
When you're thinking about like a uterine dehi C-section CT is the imaging
39:13
modality of choice, but this patient was still pregnant. Um,
39:17
and so it's really important to monitor these patients.
39:20
Once the combined thickness of the myometrium and the bladder dome get
39:25
between four and six millimeters combined,
39:27
you have to monitor these patients very closely because they are at,
39:31
at seriously high risk of true dehiscence,
39:34
uterine rupture and significant postpartum coverage.
39:37
So this patient does not technically have a diagnosis of uterine dehiscence.
39:41
She has marked myometrial thinning, which may progress to uterine dehiscence,
39:45
but she's still being monitored very closely prior to delivering.
39:51
Let's switch gears one more time. This is the last component of our OB pry.
39:56
Now we're gonna talk about gestational trophoblastic disease.
39:59
Before I take your questions,
40:01
gestational trophoblastic disease can be classified as either benign or
40:05
malignant, right?
40:06
You probably remember studying these different conditions if you were in medical
40:10
school or during residency. And so the benign, uh,
40:14
classifications of gestational trophoblastic disease,
40:16
which I'll refer to as GT V from here on out include complete MO or
40:21
partial mole malignant trophoblastic disease or gestational trophoblastic
40:26
neoplasia,
40:26
which I'll refer to here on out as GT N includes invasive mo
40:31
choriocarcinoma, placental site trophoblastic tumor,
40:34
and epithelioid trophoblastic tumor.
40:37
And what I'd like to point out is that the pathophysiology of gestational
40:41
trophoblastic disease is very similar to placenta accreta spectrum
40:46
in the sense that all G T D originates from placental trophoblast,
40:51
which are the cells which are migrating abnormal in placenta accreta spectrum,
40:55
same cell lineage that's responsible here.
41:00
Let's talk first about worm mole. It can either be complete or partial mole.
41:04
And I have some path images here, um, to show the spectrum.
41:08
So a complete mole, you'll see early uniform enlargement of a potential vili.
41:13
There are no villous capillaries here in a partial mole,
41:17
you do have a functioning circulation, a functioning villus circulation.
41:21
You may, um,
41:22
in many cases also see identifiable fetal or embryonic tissue
41:29
imaging findings for molar pregnancy, including enlarged uterus,
41:33
a heterogeneous endometrial canal with that snowstorm or Swiss cheese
41:37
appearance, which is a buzzword on exams.
41:39
You can also see hyper vascularity of the endometrial canal.
41:43
And in a molar pregnancy, um, you may not see a normal embryo.
41:47
Many of these patients will also have bilateral fecal lutein sits.
41:52
And that's because of hyperstimulation from elevated beta H c g, uh,
41:56
from the trophoblasts.
42:01
But this is the case, oh, sorry, I my watch. Ok,
42:04
so this is a case of molar pregnancy. This is the ultrasound image, right?
42:09
And we can see that this patient has an expanded endometrial cavity,
42:13
all of these cystic spaces. Um, and this nicely matches the gross specimen, um,
42:18
for this patient, which has this kinda cystic CT of brace appearance.
42:23
Oops, sorry. Um, this is another case of, um,
42:27
a patient with more pregnancy. This is the ultrasound.
42:31
We can see again those cystic spaces with some vascularity on the ultrasound
42:35
image.
42:35
And then this is a DT where we see intervening enhancing tissue in a background
42:40
of the cystic cluster of grave spaces.
42:45
This is an mri, um, for a similar patient. Um,
42:49
and we have the gross specimen to correlate with it.
42:53
And so on the SAG T two weighted image, we can see, um,
42:56
all of the cystic foci expanding the endometrial cavity.
43:00
Here's the corresponding ultrasound and then the gross.
43:07
Here's another example. We're looking at post contrast t1, um,
43:11
images where we can see again cystic spaces with intervening
43:15
heterogeneously enhancing tissue.
43:18
This is a T2 weighted image of the pelvis, um, where we can see, again,
43:22
a lot of cystic foci within this soft tissue lesion.
43:26
We can also see some fetal parts here within the endometrial
43:31
cavity. Um, and then on the axial T2 weighted image,
43:34
I also wanna point out the, um, really enlarged appearance of both ovaries.
43:40
Um, which, uh, is, um,
43:43
indicative of the bilateral fecal
43:47
treatment of molar pregnancy. Um,
43:50
includes suction and dilation curettage d dnc.
43:53
They also follow the beta HCG to zero complications of this include
43:57
invasive mole, which develops in 15 to 20% of complete moles.
44:01
Less than 5% of partial moles and choal carcinoma can develop in five to 8% of
44:06
complete moles, less than 1% of partial moles.
44:09
So complete mole has a much higher risk of progressing to either invasive mole
44:13
or choal carcinoma.
44:17
The figo criteria for diagnosis of post molar gestational trophoblastic
44:22
neoplasia include a plateau of the beta HCG levels lasting longer than four
44:27
measurements over a period of three weeks or longer rise in beta htg.
44:31
Sorry about that. Um,
44:33
for three consecutive weekly measurements over a period of two weeks or longer,
44:37
a beta HTG that's elevated for greater than or equal to six months,
44:40
or a histologic diagnosis of choal carcinoma.
44:44
This is the staging for gestational trophoblastic neoplasia. Um,
44:48
stage one is confined to the uterus.
44:50
Stage two extends outside the uterus but is limited to the genital structure.
44:55
Stage three extends to the lungs with or without genital tract involvement.
44:59
And stage four disease involves other metastatic sites. And so this patient,
45:04
uh, is at least stage three with this chest radi graft.
45:07
And then creating multiple canonball lesions in the lungs by
45:12
here's a companion case of gestational fibroblastic disease. Um,
45:16
this is a 30 year old patient with history of molar pregnancy.
45:20
She had a D N C and she presented with markedly elevated beta H C G.
45:24
We did a C2 scan for her. There's an arter, the enhancing mass,
45:28
occupying the endometrial cavity.
45:30
There's persistent enhancement here on the venous phase. Um,
45:35
and on the lung windows, the patient had multiple, uh,
45:39
metastatic pulmonary nodules.
45:41
And so this patient had a confirmed diagnosis of poeo carcinoma.
45:45
She got chemotherapy, um,
45:47
and three months later the lung nodules had significantly increased in size and
45:51
the endometrial mass had evolved.
45:56
This is a case of an invasive mole on ultrasound. Um,
46:00
so we have the gray scale image here, again,
46:02
showing this endometrial lesion that's invading the myometrium.
46:05
We have cystic spaces here that's due to the presence of the VIIs structures.
46:11
Um, and then the soft tissue is hypervascular.
46:14
And then this is the gross specimen showing the deep mytral invasion.
46:19
Here's another example of an invasive mo. Um,
46:22
we can see a mass with solid and cystic areas on the ultrasound.
46:26
And there's invasion of the myometrium on this ultrasound image.
46:30
The CT shows a lot of paper vascularity as well as Abbott enhancement.
46:35
And then we have the growth image here that shows myometrial invasion.
46:40
This is a choal carcinoma at ct.
46:42
There's a heterogeneous endometrial or myometrial mass.
46:46
You can see it sort of protruding from the right lateral aspect of the uterus.
46:51
It's really hypervascular. It has that sort of enhancing ring appearance to it.
46:55
The low density regions in the center like they represent necrosis or
46:59
hemorrhage. Um,
47:01
and we have an intraop image also showing the invasive nature of this lesion.
47:08
Here's another example. We have a T2 weighted M R i. Um,
47:12
in the superior aspect of the screen here we see a big heterogeneous uterine
47:17
mass with bilateral ovarian cysts. Do the elevated beta H c G,
47:21
we see similar findings. These are the ovarian cysts on ct.
47:24
And then this is the operative image showing the really enlarged ovaries
47:28
bilateral Last example.
47:32
This is to show that the mass may be small. Um,
47:35
so this one is T2 dark, it's due to hemorrhage,
47:39
which we can nicely see on both the gross and histopathology here.
47:43
And this patient also has lung attack disease
47:47
treatment for gestational trophoblastic neoplasia, low risk disease. Um,
47:52
these patients will get single agent chemotherapy and almost all of these
47:55
patients survive high risk disease.
47:59
That's stage four or high risk stage two or three.
48:02
They get multimodal chemotherapy, um,
48:04
with or without adjuvant surgery or radiation.
48:07
And many of these patients also do very well.
48:10
Survival rates are up to 80 to 90%.
48:15
So let's wrap things up here to conclude.
48:17
Ultrasound is the first line imaging modality in pregnancy,
48:21
but you're gonna see with these more complex cases, a lot of CT and MR.
48:26
CT is gonna help you with those incidental findings or identifying etiologies
48:31
with vague symptoms. MRI is safe during pregnancy,
48:34
it can help you characterize acute pathology.
48:37
MRI protocols for evaluating acute pathology in pregnancy should be focused and
48:42
efficient.
48:43
And then recognizing the imaging findings in each of these conditions is key to
48:47
diagnosing and treating them. These are my references.
48:51
I'd like to thank you for your time and attention. And now, uh,
48:55
let's get to the q&a. Ok.
49:00
Um, so the first one we have, um, is from an anonymous attendee. They said,
49:04
can you comment on current guidelines for imaging of suspected PE and pregnancy?
49:10
Um, so at our institution, um, we no longer, um,
49:15
perform shielding, uh, pediatric or pregnant patients. Um,
49:19
if the patient has, um,
49:22
sufficient evidence to suggest that they have a pulmonary embolism,
49:27
um, in many cases we will perform a C t a chest PE protocol.
49:32
Um, you know, we found that the really,
49:34
the risk of radiation to the patient and the fetus is, is fairly low.
49:38
And so we go ahead with the C T A.
49:43
Um, I have one question that says,
49:45
do they keep the ectopic intraabdominal pregnancy? Um,
49:49
so I'm not sure what exactly you mean by this question, but, um,
49:53
so this patient did choose to, uh,
49:56
pursue the pregnancy and when they, uh,
49:59
did a laparoscopy for her, um, the fetus was viable.
50:03
And so both the mother and fetus survived in this case.
50:09
I have a question from Kai Kim that says,
50:12
in the case shown teratoma and mucinous ca did surgical resection have
50:17
waited until the delivery, um,
50:21
along with percutaneous drainage to make room for the fetus to grow?
50:24
This is a great question. I love this question. So, um,
50:28
in suspected cases of ovarian cancer or ovarian neoplasms including
50:33
teratoma, uh, we never wanna puncture the lesion, right?
50:36
Cause we risk spilling the contents into the peritoneal cavity.
50:40
You could get peritonitis if you rupture a dermoid. Um,
50:44
you could also potentially seed the peritoneal cavity if you have a malignant
50:48
ovarian lesion. The second part of this question says,
50:52
what is the cutoff gestational age for the fetus to do reasonably well if
50:56
delivery is the only option? Um, so,
50:58
so if you chose to deliver this fetus and you know,
51:01
and then manage the ovarian tumor, um,
51:04
we try to get patients to at least 28 weeks.
51:07
But really 32 weeks is a goal where the fetus does a lot better, um,
51:11
once they're delivered with NICU care. Um, for this patient,
51:14
she was having intermittent pain. They,
51:16
they were worried that she may eventually force the ovary,
51:20
which would provide a more emergent trip to the OR for her.
51:23
And so they chose to laparoscopically resect this ovarian lesion. Um,
51:27
and then she delivered, uh, at like 38 weeks later in her pregnancy.
51:35
Um, we have a question that says,
51:36
how do you approach justifying CT examinations in pregnancy,
51:39
especially with contrast? This is a great question.
51:41
There's a lot of controversy about doing CT for pregnant patients. Um,
51:47
the bottom line is that if you think the patient has a condition that is severe
51:51
enough and urgent enough that they would be taken for a procedure or a surgery
51:56
or some kind of emergent management, um,
51:58
you have to weigh the risk of not doing that imaging with, um,
52:03
the risk of potentially, you know, exposing the fetus to radiation. Now,
52:07
CT contrast is not as big of a deal as gadolinium based.
52:11
MR contrast in terms of fetal exposure. Um,
52:14
there's less convincing data that the fetus could be harmed by administration of
52:18
IOD donated CT contrast. Um,
52:21
there's also emerging data to show that, um, you know,
52:24
really recalculating some of the radiation exposure data we largely
52:29
have from Roland Nagasaki, um,
52:31
is that some of the fetal exposures that we have previously estimated on CT are
52:36
probably as not as great as they were, um, estimated to be in the past.
52:41
That being said,
52:42
fetal radiation exposure is still a serious consideration when you're thinking
52:46
about ordering an imaging study,
52:47
but you have to weigh the risks and benefits of imaging versus not imaging based
52:52
on the patient's clinical condition.
52:55
We have a question about placenta and creta spectrum is my favorite. Um,
52:59
what are the more reliable signs on M R I for placenta aquita spectrum and
53:03
what's the best gestational age window for imaging this diagnosis?
53:07
So the features of placenta aquita spectrum on M R I will include placental
53:12
heterogeneity, abnormal placental, vascularity,
53:16
placental bands, which are probably placental inks or hemorrhage.
53:21
You'll also see myometrial thinning,
53:24
placental bulge and abnormal or rounded placental contour.
53:29
And then in cases of more advanced p a s,
53:31
you may also see invasion of adjacent structures like the bladder,
53:35
vagina or abdominal wall.
53:37
The best gestational age window for imaging placenta accreta spectrum is in the
53:41
second trimester.
53:42
We like to image these patients somewhere between 24
53:47
and 28 weeks gestation,
53:49
and that gives us plenty of time to plan for a delivery that usually happens
53:52
around 32 to 34 weeks.
53:57
Next question. What are the M R I features of ovarian torsion? Um,
54:01
so they're similar to the features that you'll see on ultrasound and ct.
54:05
You'll see an enlarged indemnities ovary.
54:08
You may see peripheral displacement of the ovarian follicles.
54:12
You can see peri uh, peri follicular, um, hemorrhage. Um,
54:17
you can see free fluid in the pelvis and the patient will often have exquisite
54:20
pelvic pain.
54:21
Sometimes on I or p coronal images are so good that you can see even that
54:26
twisting or whirlpool sign in the vascular pedicle of the taurist ovary.
54:31
And I have a case ovarian corgen in my high-risk OB course on modality if you're
54:35
interested in seeing it. Next question is non-contrast.
54:40
M r i safe for the first trimester as well? Yes.
54:43
So you can do an M r I in any trimester of pregnancy, um,
54:47
and is considered safe.
54:51
Next question,
54:53
can we differentiate between a hemorrhagic cyst and an endometrioma? Yeah,
54:57
this is a great question. Um, so endometriosis is a chronic condition. You know,
55:02
patients will have, um,
55:03
cyclic pelvic pain and it's important to be able to diagnose a hemorrhagics from
55:08
an endometrioma on imaging. Um, so on ultrasound, um,
55:12
hemorrhagics have a very classic appearance, right?
55:14
They have a lace like internal appearance and endometrioma will have
55:19
low level homogeneous internal echoes.
55:22
That's called the chocolate cyst sign of an endometrioma. On an mri,
55:26
the diagnosis can be a little bit more challenging because both of the,
55:32
um, lesions will look bright on T1 weighted imaging. Um,
55:36
but a hemorrhagic cyst will resolve and an endometrioma will also
55:40
have usually other features, um, like T2 shading, um,
55:45
which is a common feature of endometrioma.
55:47
You may see other sites of endometriosis in the public,
55:49
which may sway you as well. Uh,
55:52
Kai Kim is asking for the reference pages again, here they are.
55:55
I'll put this one up and then I'll switch to the next one. Um, let's see.
56:00
Uh, what is the full form of p a s? Um, it is,
56:06
uh, placenta accreta spectrum. Some people will call it, um,
56:10
placenta accreta spectrum disorder or P A S D. I apologize for the abbreviation.
56:18
Next question.
56:20
You have shown some intrabdominal topics to these cases, um,
56:25
opt to continue the pregnancy or should they be terminated for fear of rupture?
56:29
Um, this is something that is largely up to the patient. Um,
56:33
the team obviously would recommend in these cases that the pregnancy be
56:37
terminated because of the risk of rupture and catastrophic hemorrhage.
56:42
Um,
56:42
but obviously as physicians we can only make recommendations to our patients.
56:46
Their, it's their body and, and they have a choice about what they can do, um,
56:51
to manage any of their medical conditions.
56:53
And so this patient opted to continue her pregnancy despite the risk of rupture
56:57
hemorrhage and she got really lucky, um,
56:59
that she did not suffer a catastrophic bleed.
57:04
Um, next question. Uh, we have um,
57:06
what is the evaluation of placenta in creta? A preta and perreta? Um,
57:12
so this is a diagnosis that is first encountered often on,
57:17
um, ultrasound.
57:19
So the patient will come in usually for their anatomy scan or, uh, for,
57:23
you know, late first trimester scan and they'll see an abnormal placenta.
57:28
There are very characteristics of a, uh,
57:30
very characteristic findings of a normal placenta on ultrasound. Um,
57:34
there's this zone, um, um,
57:37
hypo aoic signal that's deep to placenta called the retro placental
57:42
clear space. Um,
57:43
and on ultrasound you'll see that space kind of disappear and you'll see
57:48
placental tissue extending toward the myometrium. And often that's good enough,
57:52
but in some cases if they're not able to see the placenta,
57:55
well if it's a complex case and they think that there is placenta perreta with
58:00
an invasion of adjacent structures, if the placenta is posterior,
58:03
which is notoriously challenging on ultrasound, they'll do mri.
58:07
And our MR protocol is a multiplanar t2, um,
58:12
weighted imaging.
58:13
And so we will do steady state precession and also turbo spin echo images for
58:17
these patients.
58:18
And so it's just multiplanar sagittal coronal and axial steady state precession
58:24
and turbo spin echo.
58:26
Some places will add diffusion weighted imaging or non-contrast t1.
58:31
I don't know that they're necessary.
58:34
So your goal of doing an M R I for a patient with placenta accreta spectrum is
58:38
to determine number one,
58:40
that there truly are features of placenta accreta spectrum present, but two,
58:44
to exclude a diagnosis of placenta for accreta.
58:49
Any other questions? Thanks so much for engaging and for,
58:53
and for asking such great questions.
58:55
I really appreciate your time and attention.
58:58
Thank you so much, uh, for your lecture today, Dr. Gomez.
59:02
Thank you so much and thanks to everyone, uh,
59:05
for participating in our noon conference.
59:07
You can access the recording of today's conference and all our previous noon
59:11
conference by creating a free m r I online account.
59:15
Be sure to join us next week on Thursday, June 22nd at 12:00 PM Eastern,
59:20
featuring Dr.
59:21
Emily f Conant for a lecture on abbreviated breast MRI for
59:26
supplemental screening early outcomes and tips for implementation.
59:30
You can register for this free lecture@mrionline.com and follow us on social
59:35
media for updates on future noon conferences. Thanks again and have a great day.