منابع مشابه
A Rare Cause of Splenomegaly: Malignant Fibrous Histiocytoma
Here we report a 38 year old male who was evaluated for splenomegaly and diagnosed to have malignant fibrous histiocytoma of spleen, which was confirmed histopathologically. Very few cases of MFH have been reported.
متن کاملOsteopoikilosis: a rare cause of bone pain
Background: Osteopoikilosis (OPK) is a rare inherited condition of the bones, transmitted as an autosomal dominant trait characterized by numerous hyperostotic areas that tend to localize in periarticular osseous regions. It is usually asymptomatic and is often diagnosed incidentally during x-rays made by other reasons. We present a case of 34-year-old man suffering from polyarthralgia an...
متن کاملan uncommon cause of splenomegaly
a 55-year-old man presented with pain in the left flank for the last 8 months with history of significant weight loss. the pain was relieved on assuming a knee-chest position. on clinical examination the patient was afebrile with mild tenderness in the left hypochondrium. there was no icterus or lymphadenopathy. the spleen was palpable 6 cm below the costal margin and was firm and non-tender. t...
متن کاملAn Uncommon Cause of Splenomegaly
A 55-year-old man presented with pain in the left flank for the last 8 months with history of significant weight loss. The pain was relieved on assuming a knee-chest position. On clinical examination the patient was afebrile with mild tenderness in the left hypochondrium. There was no icterus or lymphadenopathy. The spleen was palpable 6 cm below the costal margin and was firm and non-tender. T...
متن کاملGaucher’s Disease, an Unusual Cause of Massive Splenomegaly, a Case Report
Background Gaucher’s Disease (G.D.) is an autosomal recessive disorder resulting from the accumulation of glucocerebrosidase in the cells of macrophage-monocyte system as a result of a deficiency in lysosomal glucocerebrosidase. This enzyme is encoded by a gene on chromosome-1. Here we report a case of Gaucher’s Disease .G.D is rare in Yazd. Case reports We reported a patient that presented...
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ژورنال
عنوان ژورنال: Deutsches Aerzteblatt Online
سال: 2018
ISSN: 1866-0452
DOI: 10.3238/arztebl.2018.0116b