| Literature DB >> 20467181 |
Kayoko Ishihara-Kawase1, Toshiho Ohtsuki, Sayaka Sugihara, Hitomi Tanaka, Takeshi Nakamura, Akiro Kimura, Masayasu Matsumoto.
Abstract
Paroxysmal nocturnal hemoglobinuria is a rare acquired disorder of clonal hematopoietic stem cells and it is characterized as a hypercoagulable disorder. We report a 36-year-old woman with the rare triad of paroxysmal nocturnal hemoglobinuria, cerebral sinus thrombosis triggered by infection, and rapid-onset heparin-induced thrombocytopenia after resensitization of heparin. This case raises caution for heparin-induced thrombocytopenia in paroxysmal nocturnal hemoglobinuria.Entities:
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Year: 2010 PMID: 20467181 DOI: 10.2169/internalmedicine.49.3053
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271