Journal
AMERICAN JOURNAL OF HEMATOLOGY
Volume 67, Issue 2, Pages 139-143Publisher
WILEY-LISS
DOI: 10.1002/ajh.1093
Keywords
tuberculosis; immune thrombocytopenic purpura; idiopathic thrombocytopenic purpura
Categories
Ask authors/readers for more resources
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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available