| Literature DB >> 23765512 |
L Sanz-Canalejas1, E Gómez-Mampaso, R Cantón-Moreno, C Varona-Crespo, J Fortún, F Dronda.
Abstract
Peliosis hepatis is a rare histopathological entity of unknown etiology. We present a case of peliosis hepatis in a 44-year-old man with disseminated tuberculosis and acquired immunodeficiency syndrome. The diagnosis of peliosis hepatis was based on liver biopsy results which were suggestive of tuberculous etiology. Diagnosis of tuberculosis was confirmed by auramine stain, rRNA amplification and culture of Mycobacterium tuberculosis from synovial fluid of the elbow joint. The patient responded favourably to tuberculostatic treatment with four drugs and the early initiation of highly active antiretroviral therapy. Histopathological evidence of peliosis hepatis, without an obvious cause, makes it necessary to rule out tuberculosis, especially in the context of immunodeficiency diseases and immigrants from endemic areas.Entities:
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Year: 2013 PMID: 23765512 DOI: 10.1007/s15010-013-0490-3
Source DB: PubMed Journal: Infection ISSN: 0300-8126 Impact factor: 3.553