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essential thrombocythemia following immune thrombocytopenia with jak2 v617f mutation: a case report
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نویسنده
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payandeh mehrdad ,aeinfar mehrnoush ,dadashizadeh kimiya ,yari saba
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منبع
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case reports in clinical practice - 2021 - دوره : 6 - شماره : 4 - صفحه:141 -144
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چکیده
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Immune thrombocytopenia (itp) is an autoimmune bleeding disorder. tyrosine kinase jak2 (jak2 v617f) mutation occurs in nearly 60% of essential thrombocythemia (et) patients. both diseases produce impaired platelet. we describe a case with et following itp. so far, only 3 reports described et following itp. we report the fourth patient with jak2 v617f mutation at the onset of itp presented 20 years ago that needed splenectomy. the association of these two diseases may recommend similar pathogenic mechanisms between myeloproliferative neoplasms (mpns) and itp that should be further explored.
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کلیدواژه
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jak2 mutation; essential thrombocythemia; immune thrombocytopenia
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آدرس
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kermanshah university of medical sciences, department of hematology and medical oncology, iran, kermanshah university of medical sciences, medical biology research center, iran, university of maragheh, faculty of science, department of biology, iran, university of maragheh, faculty of science, department of biology, iran
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پست الکترونیکی
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sabayari95@gmail.com
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Authors
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