Literature DB >> 870977

Sickle cell hepatopathy.

T W Sheehy.   

Abstract

Hepatic dysfunction is a common finding in patients with sickle cell disease but viral hepatitis appears to be an unusual complication in the adult SS patient. Only five cases of viral hepatitis were recorded in 378 admissions for SS crisis. In contrast, hepatic crisis occurred as a distinct event in 9% of 88 patients with sickle cell anemia. This entity must be differentiated from acute cholecystitis or viral hepatitis. Transiently abnormal results of hepatitic function tests were observed in another 26 patients with extrahepatic crisis. Cirrhosis is relatively common and often the terminal event in SS disease. Choledocholithiasis and cholecystitis are infrequent complications despite the prevalence of gallstones in SS anemia.

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Year:  1977        PMID: 870977     DOI: 10.1097/00007611-197705000-00008

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  22 in total

1.  Reversal of hepatic and renal failure from sickle cell intrahepatic cholestasis.

Authors:  Muhammad A Khan; John A Kerner
Journal:  Dig Dis Sci       Date:  2011-01-26       Impact factor: 3.199

2.  Case of fatal sickle cell intrahepatic cholestasis despite use of exchange transfusion in an African-American patient.

Authors:  Daniel B Costa; Rebecca A Miksad; Michael S Buff; Yihong Wang; Bruce J Dezube
Journal:  J Natl Med Assoc       Date:  2006-07       Impact factor: 1.798

3.  Sickle Cell Intrahepatic Cholestasis with Acute Liver Failure and Acute Kidney Injury: Favourable Outcome with Exchange Transfusion.

Authors:  Prabir Maji; Rohan Malik; Rakesh Lodha; Arvind Bagga
Journal:  Indian J Pediatr       Date:  2019-09-13       Impact factor: 1.967

4.  Acute on chronic liver failure in a patient with sickle cell anaemia (HbSS).

Authors:  Dana DaEun Im; Utibe Essien; Jacqueline W DePasse; Victor Chiappa
Journal:  BMJ Case Rep       Date:  2015-07-01

5.  Liver stiffness increases acutely during sickle cell vaso-occlusive crisis.

Authors:  Christopher Koh; Tiffany Turner; Xiongce Zhao; Caterina P Minniti; Jordan J Feld; Jennifer Simpson; Mary Demino; Anna K Conrey; Mary J Jackson; Catherine Seamon; David E Kleiner; Gregory J Kato; Theo Heller
Journal:  Am J Hematol       Date:  2013-08-01       Impact factor: 10.047

6.  Acute hepatic sequestration in sickle cell disease.

Authors:  William E Norris
Journal:  J Natl Med Assoc       Date:  2004-09       Impact factor: 1.798

7.  Reversal of liver function without exchange transfusion in sickle cell intrahepatic cholestasis.

Authors:  Nattamol Hosiriluck; Supannee Rassameehiran; Erwin Argueta; Lukman Tijani
Journal:  Proc (Bayl Univ Med Cent)       Date:  2014-10

8.  Definitions of the phenotypic manifestations of sickle cell disease.

Authors:  Samir K Ballas; Susan Lieff; Lennette J Benjamin; Carlton D Dampier; Matthew M Heeney; Carolyn Hoppe; Cage S Johnson; Zora R Rogers; Kim Smith-Whitley; Winfred C Wang; Marilyn J Telen
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

Review 9.  Acute liver function decompensation in a patient with sickle cell disease managed with exchange transfusion and endoscopic retrograde cholangiography.

Authors:  Haris Papafragkakis; Mel A Ona; Kinesh Changela; Swayamprabha Sadanandan; Abraham Jelin; Sury Anand; Sushil Duddempudi
Journal:  Therap Adv Gastroenterol       Date:  2014-09       Impact factor: 4.409

10.  Pathological spectrum of liver diseases in sickle cell disease.

Authors:  M Omata; C S Johnson; M Tong; D Tatter
Journal:  Dig Dis Sci       Date:  1986-03       Impact factor: 3.199

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