期刊
AMERICAN JOURNAL OF HEMATOLOGY
卷 67, 期 2, 页码 139-143出版社
WILEY-LISS
DOI: 10.1002/ajh.1093
关键词
tuberculosis; immune thrombocytopenic purpura; idiopathic thrombocytopenic purpura
类别
We report the case of a 49 year-old male who presented with immune thrombocytopenia (ITP)-induced epistaxis and generalized purpura, During the same hospitalization the patient was also found to have clinical, microbiological, histological, and roentgenographic evidence of disseminated mycobacterial tuberculosis (TB). The hematological and infectious abnormalities, which did not respond to high-dose intravenous corticosteroids end immune globulin (IVIg), resolved after anti-tuberculous treatment. Herein we review the characteristics of this rarely documented association. Am. J. Hematol. 67:139-143, 2001. (C) 2001 Wiley-Liss, Inc.
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