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Caroli’s Disease

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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.

Report

Faculty

Mahan Mathur, MD

Associate Professor, Division of Body Imaging; Vice Chair of Education, Dept of Radiology and Biomedical Imaging

Yale School of Medicine

Tags

Vascular

Other Biliary

MRI

Liver

Idiopathic

Gastrointestinal (GI)

Congenital

CT

Body

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