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Pathology · Haemodynamics: Budd-Chiari syndrome
Sample itemA 32-year-old woman with polycythaemia vera develops painful hepatomegaly and rapidly accumulating ascites. Doppler shows no flow in the hepatic veins. Which histological finding is expected in the liver?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Centrilobular congestion with sinusoidal dilatation and haemorrhagic necrosis
Hepatic vein thrombosis obstructs outflow, so blood backs up into the central veins and zone 3 sinusoids. Centrilobular congestion, hepatocyte atrophy and haemorrhagic necrosis follow, and fibrosis develops with time. Myeloproliferative disorders such as polycythaemia vera and paroxysmal nocturnal haemoglobinuria are important causes.
Option by option
A. Centrilobular congestion with sinusoidal dilatation and haemorrhagic necrosis (correct)
Correct. Outflow obstruction produces a centrilobular congestive and haemorrhagic pattern.
B. Loss of interlobular bile ducts with granulomatous cholangitis
Bile duct loss with granulomatous cholangitis is primary biliary cholangitis, not a thrombotic disorder.
C. Periportal piecemeal necrosis with a dense plasma-cell infiltrate
Piecemeal necrosis with plasma cells is autoimmune hepatitis, a periportal inflammatory disease.
D. Periportal Mallory-Denk bodies with micronodular cirrhosis
Mallory-Denk bodies with cirrhosis indicate alcoholic liver disease, which is not suggested by the history.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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