نتایج جستجو برای: splenomegaly

تعداد نتایج: 3944  

Journal: :the journal of tehran university heart center 0
rezayat parvizi cardiovascular research centre, tabriz university of medical sciences, tabriz, iran. rasoul ibrahim abdulrahman cardiovascular research centre, tabriz university of medical sciences, tabriz, iran. rezvaneh salehi cardiovascular research centre, tabriz university of medical sciences, tabriz, iran. ghader shah mohamadi cardiovascular research centre, tabriz university of medical sciences, tabriz, iran.

splenomegaly-induced thrombocytopenia is fully described in hematological and surgical literature, but its association with severe aortic stenosis is rare. we present a case of severe aortic valve stenosis with severe splenomegaly-induced thrombocytopenia in which aortic valve replacement was done with a number 23 homograft and splenectomy was performed after the end of cardiopulmonary bypass. ...

Journal: :Proceedings of the Royal Society of Medicine 1910

Journal: :Proceedings of the Royal Society of Medicine 1940

2016
Mi-Jung Kim Sae-Won Han Dae-Won Lee Yongjun Cha Kyung-Hun Lee Tae-Yong Kim Do-Youn Oh Se Hyung Kim Seock-Ah Im Yung-Jue Bang Tae-You Kim

PURPOSE Splenomegaly is a clinical surrogate of oxaliplatin-induced sinusoidal obstruction syndrome (SOS). We investigated development of splenomegaly and its association with treatment outcome and genetic polymorphisms following adjuvant 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) in colorectal cancer (CRC) patients. MATERIALS AND METHODS Splenomegaly was determined by spleen volume...

Journal: :Hematology Reviews 2021

Many diseases can induce splenomegaly, however, about 5% of splenomegalies are idiopathic. When there is no underlying treatable cause, and the splenomegaly significantly affects quality life, splenectomy best therapeutic choice. A 67-year-old woman had idiopathic asymptomatic splenomegaly. The increase in resulted hypersplenism with cytopenia symptoms related to abdominal discomfort. patient u...

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...

Journal: :Proceedings of the Royal Society of Medicine 1964

Journal: :Proceedings of the Royal Society of Medicine 1937

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