| Literature DB >> 14978693 |
G Pappas1, M Kitsanou, L Christou, E Tsianos.
Abstract
Thrombocytopenia often complicates the course of acute brucellosis, mainly due to bone marrow suppression or hypersplenism. Immune thrombocytopenia is also reported in brucellosis, resulting usually in massive thrombocytopenia, purpura, and spontaneous hemorrhage. We describe a case of acute brucellosis in an 85-year old woman, who presented with fever, purpuric skin lesions, anemia, and rhinorrhagia. The absolute platelet count was 1000/microL. Direct and indirect Coombs tests were positive, and a cold-agglutinin was detected. The patient was diagnosed as suffering from brucellosis on the basis of a strongly positive serologic reaction and was treated with doxycycline, streptomycin, and a short course of corticosteroids, with a rapid rise in platelet number. Copyright 2004 Wiley-Liss, Inc.Entities:
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Year: 2004 PMID: 14978693 DOI: 10.1002/ajh.10473
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047