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Rare presentation of refractory thrombotic thrombocytopenic purpura: Jejunal stricture
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نویسنده
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abeysundara p.k. ,athukorala i. ,dalpatadu k.p.c. ,balendran k. ,dilrukshi m.d.s.a. ,fernando g.m.o.
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منبع
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international journal of hematology-oncology and stem cell research - 2017 - دوره : 11 - شماره : 4 - صفحه:293 -295
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چکیده
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Thrombotic thrombocytopenic purpura is a rare thrombotic disease characterized by episodes of thrombocytopenia and microangiopathic hemolytic anemia due to disseminated microvascular thrombosis. thrombotic thrombocytopenic purpura was first described in 1924 by moschowitz as a disease presenting with a pentad of signs and symptoms (anemia,thrombocytopenia,fever,hemiparesis and hematuria). previous studies have described atypical manifestations of thrombotic thrombocytopenic purpura such as hemolysis,anemia and thrombosis. © 2017 international journal of hematology-oncology and stem cell research,all right reserved.
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کلیدواژه
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Chron’s-disease; TTP
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آدرس
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postgraduate institute of medicine,university of colombo,colombo, Sri Lanka, faculty of medicine,university of colombo,colombo, Sri Lanka, faculty of medicine,university of colombo,colombo, Sri Lanka, postgraduate institute of medicine,university of colombo,colombo, Sri Lanka, postgraduate institute of medicine,university of colombo,colombo, Sri Lanka, postgraduate institute of medicine,university of colombo,colombo, Sri Lanka
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Authors
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