[Liver injury in idiopathic CD4+T-cell lymphocytopenia].

Keren Cohen*, Ruth Hadary, Lotan Shilo, Alla Shabun, Oded Kimchi, Yona Kitay-Cohen

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

A 48 years old patient was admitted to the Internal Medicine ward due to progressive weakness and abnormal liver function tests. During three months of hospitalization she developed opportunistic infections with Cryptococcus and Pneumocystic jiroveci pneumonia. The CD4+ T-cell lymphocyte count was very low with no evidence of infection with human immunodeficiency virus. Liver disease deteriorated with the appearance of profound jaundice and severe hepatitis. The patient's laboratory and clinical presentation were compatible with the diagnosis of idiopathic CD4 + T-cell lymphocytopenia--ICL. The authors reviewed the literature on ICL and discuss the rare hepatic presentation of this uncommon syndrome.

Original languageEnglish
Pages (from-to)688-691, 720
JournalUnknown Journal
Volume151
Issue number12
StatePublished - Dec 2012

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