Volume 10, Number 1 (5-1996)                   Med J Islam Repub Iran 1996 | Back to browse issues page


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BANIHASHEM A, GHIASSI T, ZABIHYAN S. MALIGNANT HISTIOCYTOSIS: A CASE REPORT AND REVIEW OF THE LITERATURE. Med J Islam Repub Iran. 1996; 10 (1) :79-83
URL: http://mjiri.iums.ac.ir/article-1-1225-en.html

From the Departments of Pediatrics Ghaem Hospital, Mashhad University of Medical Sciences, Mashhad, Islamic Republic of Iran.
Abstract:   (1563 Views)
Malignant histiocytosis (MH) is a rare hematologic malignancy, especially in the first decade of life. The disease is clinically characterized by fever, hepatosplenomegaly, lymphadenopathy, pancytopenia and jaundice, and histologically by systemic proliferation of malignant histiocytes and hemophagocytosis. The prognosis is poor and often the diagnosis is not made before death. Because of the rarity of this disease, it is unusual for practitioners to diagnose it by bone marrow aspiration (BMA) alone
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Type of Study: case report | Subject: Pediatric