Unusual case of adult hemophagocytic syndrome

Unusual case of adult hemophagocytic syndrome

Hemophagocytic syndrome (HPS) is an uncommon manifestation in systemic lupus erythematosus (SLE). Clinical features of HPS include fever, pancytopenia, abnormal liver enzyme, hepatosplenomegaly, lymphadenopathy, and coagulation disorder. HPS comprises primary and reactive forms. Herein, we describe...

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Bibliographic Details
Main Authors: Babak Tamizifar, Golnaz Samadi, Maryam Rismankarzadeh
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:Journal of Research in Medical Sciences
Subjects:
Autoimmunity
hemophagocytic syndrome
hemophagocytosis
systemic lupus erythematosus
Online Access:http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2014;volume=19;issue=2;spage=178;epage=180;aulast=Tamizifar

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http://www.jmsjournal.net/article.asp?issn=1735-1995;year=2014;volume=19;issue=2;spage=178;epage=180;aulast=Tamizifar

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