sickle cell hepatopathy

sickle cell hepatopathy

the liver damage that accompanies sickle cell disease, caused especially by vascular occlusion and ischemia, sequestration, and cholestasis.

sick·le cell hep·a·top·a·thy

(sik'ĕl sel hep'ă-top'ă-thē)
Any liver disorder directly related to the sickling process of sickle cell disease and the transfusions required for its treatment. The direct manifestations are related primarily to vascular occlusion and include acute ischemia, sequestration, and cholestasis. Hepatitis and hepatic abscesses are also seen in acute sickle hepatic crisis.
References in periodicals archive ?
Sickle cell intrahepatic cholestasis (SCIC), one of the syndromes secondary to sickle cell hepatopathy, is a rare but potentially fatal complication of sickle cell disease.
Sheehy first categorized sickle cell hepatopathy in 1977 into five clinical syndromes: viral hepatitis, hepatitis crisis, cirrhosis, cholelithiasis with cholecystitis, and intrahepatic cholestasis (SCIC).
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