Interactive Transcript
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The final category of large airway disorders we will
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discuss are neoplastic disorders.
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I will show you examples of subglottic,
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infantile hemangioma, recurrent respiratory papillomatosis,
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carcinoid tumor muco epidermoid tumor
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and inflammatory myofibroblastic tumor.
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We'll start with a case of subglottic infantile
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Hemangioma.
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We have two axial MRI images,
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T two fat saturation as well
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as T one post contrast fat saturation
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And I wanna scroll down To the subglottic airway.
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There are some additional findings on this patient,
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including a hyperintense enhancing right pro gland,
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but we won't be discussing that today.
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We are instead going to focus on that subglottic airway
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Where we note Subtly that there is a small focus of
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nodular hyperintense signal on the T two
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with corresponding hyper enhancement.
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Although in this patient we've got
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Some motion artifact.
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This is a persistent finding on multiple series
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and multiple planes
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and this corresponded with some prior imaging
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that I'm not showing that included a radiograph,
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a frontal radiograph that included an asymmetric appearance
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Of the sub airway.
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Infantile hemangiomas can occur anywhere in the body,
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but something definitely
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to think about in an infant less than six months old
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who has either croup like symptoms
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but not the right age group for croup
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or sometimes seen on imaging like I mentioned on a
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radiograph with an asymmetric appearance of
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The airway.
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If you find what looks like an infantile hemangioma in the
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subglottic airway, think about syndromes,
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particularly one called faces, P-H-A-C-E-S.
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You don't need to memorize what all of those things are.
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You can always look it up, but it stands
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for posterior fossa, malformation, hemangiomas of the face,
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arterial anomalies, cardiac anomalies, eye anomalies,
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and sternal clefts or supra umbilical ra.
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Again, you don't need To memorize that,
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but do remember that a syndrome can be associated
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with airway hemangiomas.
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This next case is a different patient also
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with a subglottic airway hemangioma,
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but this time on ct,
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as we can see on the axial contrast enhanced image,
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we have a larger focus of enhancement along
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The right poster lateral airway
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Causing narrowing of the airway.
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As we see here on ct, it's important to know
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that this entity exists
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because in these very small patients it would be easy
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to miss them if they're subtle, if you're just racing
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through your study and scrolling through really quickly.
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But if you know this exists
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and if you know the patient is having some sort
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of upper airway symptoms, then keep an eye out
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for potentially small
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focal enhancing nodules in this location.
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Definitely think about a subglottic infantile hemangioma.
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This next case I'm showing you is of an older patient
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who had recurrent respiratory papillomatosis.
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This is caused by benign tumors
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of the aerodigestive tract caused by perinatal transmission
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of HPV most commonly.
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So these patients usually contract HPV from their mother
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during birth.
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This can manifest with AirWave pulmonary
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and GI tract manifestations.
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Rarely these can undergo malignant degeneration.
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The most common finding is actually in the larynx
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where you can see uh, nodules due to the HPV infection,
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but this can spread by endobronchial root
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and end up in the lungs as well.
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In this particular patient,
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we can see in the distal airway a little bit
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of soft tissue nodularity just above the Karina
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and that represents papilloma of this papillomatosis.
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But the more obvious finding in this particular patient is
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the lung involvement.
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We can see multifocal nodular opacities throughout both
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lungs, many of which cavitate,
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and that is a finding that can occur with papillomatosis.
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You can have solid nodules, you can have cavitary nodules,
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and you can have a combination like we see in this patient.
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So important to know that this can be limited
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to the airways, but it also can end up in the lungs
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and so be on the lookout for either finding.
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The next tumor I'm gonna show you
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is an endobronchial lesion.
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I'm gonna start with the coronal CT here.
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Contrast enhanced ct. We have a lot going on,
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but what I'll focus in on first as we sort
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of change the windows a little bit here is this soft tissue
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nodular density within the right main bronchus.
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This is a carcinoid tumor
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and we can see in this particular patient in addition
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to the endobronchial component of the lesion right here,
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causing airway narrowing, it also extends
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beyond the confines of the airway.
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And we can also see associated
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with this lobular soft tissue mass, quite a bit
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of post obstructive atelectasis.
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So carcinoid tumor is a neuroendocrine tumor
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with metastatic potential.
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It can occur in a lot of places,
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but the airways is one of those places.
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We can see calcifications occasionally with these lesions.
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We don't see that here with this patient
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and we can expect to see quite a bit
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of enhancement of the lesion.
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We can see endobronchial lesions like we see in our patient,
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but we sometimes don't see an endobronchial component
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and we instead see a hilar component or a hilar mass.
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Um, and occasionally you can also see solitary pulmonary
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nodules if it's arising further out in the distal airways.
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In our patient, like I mentioned,
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we see post obstructive atelectasis here, quite a bit
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of enhancing atelectatic tissue,
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which I'll also confirm here on the sagittals.
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But in these patients we can also sometimes see air trapping
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bronchiectasis or even mucus plugging in those airways.
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This next patient also has an endobronchial lesion,
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but this is a different lesion.
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Again, we'll start with the coronal here
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and we'll see in that same right bronchus
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that there is an endobronchial soft tissue lesion,
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nonspecific perhaps a little bit less enhancing than the
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carcinoid, and this is a muco epidermoid tumor.
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These can have variable enhancement.
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They also can have calcifications
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In this particular patient.
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We don't see calcifications of the endobronchial lesion,
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but we have quite a bit
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of calcification in surrounding mediastinal
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and hilar lymphadenopathy.
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Give a better demonstration of that lymphadenopathy.
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We'll go to the axials.
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We see the contrast in the vascular structures here,
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and then we have SubCal
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and perihilar calcification as well
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as left perihilar calcification as well.
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Although not seen in this particular patient.
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Uh, we can have post obstructive atelectasis
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and our patient instead, we have more of a post
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obstructive air trapping type picture.
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Our final two cases are two different patients
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with the same entity.
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We'll start with this patient's chest radiograph.
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You can see that there's an obvious density in the left
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lower lung with associated calcification
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or partial calcification of this mass.
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It's important to note in this patient
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that the ribs look pretty normal, they don't look eroded,
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and they also don't look bizarrely shaped or dysplastic.
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The reason I mention that is that there is a rare tumor
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of childhood, uh, called mesenchymal hematoma
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and that can present with a large chest mass
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with calcification, but classically
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has associated bizarre dysmorphic appearance
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of the adjacent ribs in this patient.
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The ribs look pretty preserved.
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This patient went on to get a CT scan with IV contrast,
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and we'll start with the axial image.
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We can see that there's this large soft tissue mass
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occupying much of the left chest with a lot
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of internal calcification,
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as we noted on the chest radiograph,
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and this was an inflammatory myofibroblastic tumor,
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also known as an inflammatory pseudotumor
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or plasma cell granuloma.
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This is a spindle cell tumor
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with intermediate malignant potential.
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It can arise in many different organs in the body, and
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although primary lung tumors are extremely rare in children,
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this is the most common
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of the primary lung tumors in pediatric patients.
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The appearance is variable.
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It can have a heterogeneous enhancing appearance.
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It can have calcifications
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as we see in this particular patient.
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Unfortunately, the prognosis is quite good if there's
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complete surgical resection.
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The final patient I'll show you also has the same diagnosis
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of inflammatory myofibroblastic tumor.
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This is an older child
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and this first radiograph is not in your viewer,
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but I'm showing for your reference.
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They had a procedure for pectus excavatum,
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and this is a pectus bar.
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This was an immediate post procedure radiograph
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with a pneumothorax,
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which is not uncommonly seen immediately
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after a pectus procedure.
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So just keep in mind that this is
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what their chest radiograph looked like.
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Two years later. They were having follow up
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for their pectus surgery and had this radiograph
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and suddenly there's a new dense right chest
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opacity that was not there on the prior, so they went on
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to also get a CT scan.
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We could see in this patient, unlike our prior patient
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that had more of a heterogeneous enhancing appearance,
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this one has a more uniformly hypodense appearance.
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For most of it, there are no calcifications like we saw in
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our prior patient, but this also was the same diagnosis,
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inflammatory myofibroblastic tumor on lung windows.
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We can again see the mass.
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We see a little bit of ectasis of the lung adjacent to it,
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but none of the other findings we saw in our prior patient.
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So this just illustrates the range of appearances
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that this tumor can have.