Familial hemophagocytic lymphohistiocytosis in two brothers

Gan, Gin Gin and Eow, Geok Im and Teh, A. and Ng, S.C. and Sangkar, J.V. (2004) Familial hemophagocytic lymphohistiocytosis in two brothers. Medical Journal of Malaysia, 59 (1). pp. 100-102. ISSN 0300-5283

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Abstract

Familial hemophagocytic lymphohistiocytosis is a disorder which presents with fever, pancytopenia, liver dysfunction and also an increase in non-malignant histiocytes with prominent hemophagocytosis in various organs. It is usually difficult to distinguish from other hemophagocytic syndrome in the absence of family history. It rarely manifests in adults. Chemotherapy is usually indicated. Here, we report the occurrence of this disorder in two brothers in their twenties.

Item Type: Article
Additional Information: DH
Uncontrolled Keywords: Familial hemophagocytic lymphohistiocytosis; hemophagocytic syndrome
Subjects: R Medicine
Divisions: Faculty of Medicine
Depositing User: Mr Jasny Razali
Date Deposited: 12 Mar 2021 07:22
Last Modified: 12 Mar 2021 07:22
URI: http://eprints.um.edu.my/id/eprint/24581

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