| Literature DB >> 29667721 |
Lydia H Pecker1, Nidhi Patel2, Susan Creary3, Anil Darbari4, Emily Riehm Meier5, Deepika S Darbari6, Ross M Fasano7.
Abstract
The hepatic complications of sickle cell disease (SCD) are associated with increased morbidity and mortality in adults; children usually survive but may suffer significant sequelae. Few diagnostic tools differentiate the various hepatic manifestations of SCD. Why patients exhibit one hepatic pathology versus another is unclear. We report four pediatric patients with hemoglobin SS disease with diverse manifestations of acute hepatic involvement including acute sickle hepatic crisis, hepatic sequestration, sickle cell intrahepatic cholestasis, and a non-SCD cause of hepatopathy in a patient with viral hepatitis. These complications require a systematic approach to extensive evaluation and coordinated multidisciplinary care.Entities:
Keywords: sickle cell anemia; sickle cell disease; sickle hepatopathy
Mesh:
Year: 2018 PMID: 29667721 DOI: 10.1002/pbc.27060
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167