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Cases: Neoplastic Disorders of the Large Airway

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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.

Report

Faculty

Grace S Mitchell, MD, MBA

Pediatric Radiologist

Children's Mercy Hospital Kansas City

Tags

X-Ray (Plain Films)

Pediatrics

Neuroradiology

Neoplastic

MRI

Lungs

Chest

CT

Aerodigestive system