منابع مشابه
Autoimmune Lymphoproliferative Syndrome Misdiagnosed as Hemophagocytic Lymphohistiocytosis A Case Report
Autoimmune lymphoproliferative Syndrome (ALPS) is a rare inherited disorder of apoptosis. It usually presents with chronic lymphadenopathy, splenomegaly, and symptomatic cytopenia in a child. Herein, we report a 14-year-old boy with symptoms misdiagnosed as hemophagocytic lymphohistiocytosis who was treated before ALPS was diagnosed for the patient. This case should alert pediatricians to consi...
متن کاملHistoplasmosis-associated hemophagocytic syndrome: a case report.
Hemophagocytic syndrome is a macrophage disorder that may develop as a result of immunological activation, such as that seen in severe infection. It has been described in persons with HIV/AIDS and in those with a variety of HIV-associated opportunistic infections, including those caused by Histoplasma capsulatum. If present, this disorder may portend a poorer prognosis. We describe an HIV-posit...
متن کامل1455Histoplasmosis-induced Hemophagocytic Syndrome: A Case Series
Background. Sparse clinical data exist regarding the course and outcomes of histoplasmosis-associated hemophagocytic lymphohistiocytosis (HLH) in adults. Data from this decade are limited to case reports. The objective of this study is to describe the clinical features, treatment, and outcomes of patients with histoplasmosis-associated (HLH) at our institution in the past decade. Methods. We pe...
متن کاملUnusual 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 a case of untreated SLE with HPS as one of the first manifestations of systemic Lupus.
متن کاملunusual 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 a case of untreated sle with hps as one of the first manifestations of systemic lupus.
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ژورنال
عنوان ژورنال: Practica Oto-Rhino-Laryngologica
سال: 1997
ISSN: 1884-4545,0032-6313
DOI: 10.5631/jibirin.90.797