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Title: Hemophagocytic syndrome after living-donor liver transplantation for fulminant liver failure: a case report. Author: Taniai N, Akimaru K, Kawano Y, Mizuguchi Y, Shimizu T, Takahashi T, Mamada Y, Yoshida H, Tajiri T. Journal: Hepatogastroenterology; 2005; 52(63):923-6. PubMed ID: 15966233. Abstract: Hemophagocytic syndrome (HPS) is a hypercytokinemia caused by activated T lymphocytes and macrophages in immunologically compromised patients. We report a 37-year-old female who was diagnosed with HPS after undergoing living-donor liver transplantation (LDLT) for fulminant liver failure of unknown etiology. After liver transplantation, recipients with pancytopenia should be tested for serum ferritin. When the serum ferritin is abnormal, the bone marrow should be biopsied to screen for HPS as soon as possible. If the condition is caught early and promptly treated, the outcome of this devastating condition might be improved. In addition, HPS should be ruled out in LDLT candidates with acute liver failure before their operations.[Abstract] [Full Text] [Related] [New Search]