| Literature DB >> 19836178 |
J Sandrini1, A-B Beucher, M-C Rousselet, M Gardembas, C Lavigne.
Abstract
INTRODUCTION: The hemophagocytic syndrome is rare and sometimes associated with tuberculosis. OBSERVATION: We report the case of a 30-year-old migrant from Congo presenting with a recurrent right pleuropneumonia, cachexia and night sweat. Blood tests revealed bicytopenia with a normal myelogram. Thorax CT-scan showed large mediastinal lymph nodes and pleuritis. Mediastinal lymph node biopsy concluded to granulomatosis lymphadenopathy with necrosis and bone marrow biopsy suggested hemophagocytic syndrome. The outcome was favorable with antibiotics and corticosteroids. (c) 2009 Elsevier Masson SAS. All rights reserved.Entities:
Mesh:
Year: 2009 PMID: 19836178 DOI: 10.1016/j.medmal.2009.09.003
Source DB: PubMed Journal: Med Mal Infect ISSN: 0399-077X Impact factor: 2.152