Interactive Transcript
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So this patient is just under one year
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of age, with a history of sepsis and had a CT
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scan of the chest, abdomen, and pelvis to
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evaluate for a source of the sepsis.
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And so we'll scroll downwards and go right
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to the abdomen and the liver in particular,
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where there are a lot of abnormalities.
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And on face value, we're really just seeing
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numerous liver cysts, or cystic lesions within
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the liver, multifocal involving the right
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hepatic lobe, and involving the left hepatic lobe.
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We'll look at it a little bit closer.
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Let's follow the portal vein and
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let's follow some of its branches.
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And you can see, for example, the left portal
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vein; some of its branches are going right
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towards the center of these cystic spaces.
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So this one over here, we can follow this
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branch backwards, coming from the portal
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vein, going right towards the center.
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This one here is at the center.
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This one here is at the center.
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And so, what we're really seeing are
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multiple cystic lesions that are enveloping
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or surrounding these portal veins, these
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portal vein branches in a very young child,
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below one year of age.
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And so this entity is almost
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pathognomonic for Caroli's disease.
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And this is a congenital abnormality
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and it results in multifocal regions
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of either saccular or cystic dilatation
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of the intrahepatic bile ducts.
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It can be diffuse; it can be involving just
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one lobe, potentially involving a segment
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of one lobe, and if it's associated with
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liver fibrosis and portal hypertension,
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it's known as Caroli's syndrome.
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If it's not associated with that,
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we call it Caroli's disease.
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In imaging findings, we're seeing numerous
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liver cysts; these will communicate with
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the biliary tree; they're essentially
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abnormalities of the biliary tree themselves.
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And one of the findings that's been
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described, I believe first on ultrasound,
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but that I think sort of holds true for
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any sort of cross-sectional imaging you
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do thereafter, is the central dot sign
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where you see the portal radical really
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at the center of this saccular dilatation.
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This is often associated with diseases
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of the kidney as well, such as autosomal
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recessive polycystic kidney disease, medullary
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sponge kidney, and medullary cystic disease.
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You can see this patient definitely
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has some sort of cystic disease
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involving the right kidney.
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And the last thing I'll mention is that when
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you look at some classification schemes,
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sometimes they'll qualify this entity as a
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type 5 choledochal cyst, but it's thought that
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the pathophysiology of this is different enough
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from the other choledochal
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cysts that it's sort of classified as its own
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entity and known as Caroli's disease.
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So if you see that sort of put into that
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category, don't be surprised
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that it's sometimes put in that category,
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but it's thought to be unique enough in
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the way that it forms that it can be sort
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of classified as its own separate entity.
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And so again, this is a case of
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Caroli's disease in a very young
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child who has a history of sepsis.
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