An Atypical Case of Thrombotic Thrombocytopenic Purpura

Arzu Didem Yalcin; Ali Keskin; Hakan Erbay; Nese Aydemir

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An Atypical Case of Thrombotic Thrombocytopenic Purpura

机译：血栓性血小板减少性紫癜的非典型病例

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Thrombotic thrombocytopenic purpura (TTP) is a syndrome characterised by a classical triad of microangiopathic haemolytic anemia, thrombocytopenia and neurological symptoms. But also, it could be presented with a pentad by the addition of fever and renal failure (1, 2). There are several reports concerning the aetiology of TTP, which is not always identified (3-5). We report an unusual case of TTP in a patient who has neurological findings and impaired hepatic functions with minimal thrombocytopenia.

机译：血栓性血小板减少性紫癜（TTP）是一种以微血管病性溶血性贫血，血小板减少症和神经系统症状的经典三联征为特征的综合征。而且，它可能会伴随发烧和肾衰竭而出现五联征（1、2）。关于TTP病因的报道有很多，但并不总是能确定的（3-5）。我们报告了一名神经病学发现，肝功能受损，血小板减少症最少的患者发生TTP的异常情况。

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《The Internet Journal of Emergency and Intensive Care Medicine》 |2004年第2期|共3页
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Arzu Didem Yalcin; Ali Keskin; Hakan Erbay; Nese Aydemir;
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中图分类各部位及各科疾病的X线诊断与疗法;
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1. Atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: Clinically differentiating the thrombotic microangiopathies [J] . CatalandS.R., WuH.M. European journal of internal medicine . 2013,第6期

机译：非典型溶血性尿毒症综合征和血栓性血小板减少性紫癜：临床区分血栓性微血管病变
2. PATIENT-REPORTED OUTCOME (PRO) INSTRUMENT DEVELOPMENT FOR CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA (cTTP, UPSHAW-SCHULMAN SYNDROME [USS], HEREDITARY THROMBOTIC THROMBOCYTOPENIC PURPURA, hTTP) [J] . Oladapo A., Ito D., Hibbard C., Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research . 2017,第5期

机译：患者报告的结果（Pro）先天性血栓形成血小板减少紫癜（CTTP，Upshaw-schulman综合征[USS]，遗传性血栓性血小板减少症Purpura，HTTP）
3. PATIENT-REPORTED OUTCOME (PRO) INSTRUMENT DEVELOPMENT FOR CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA (cTTP, UPSHAW-SCHULMAN SYNDROME [USS], HEREDITARY THROMBOTIC THROMBOCYTOPENIC PURPURA, hTTP) [J] . Oladapo A., Ito D., Hibbard C., Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research . 2017,第5期

机译：患者报告的结果（Pro）先天性血栓形成血小板减少紫癜（CTTP，Upshaw-schulman综合征[USS]，遗传性血栓性血小板减少症Purpura，HTTP）
4. Clinical Case of 11 - Year-Old Child with Thrombotic Thrombocytopenic Purpura [C] . Revazova A. A., Bazrova F. V., Burnatseva M. V., International Conference on Health and Well-Being in Modern Society . 2019

机译：11岁儿童血栓形成血栓形成脓性紫癜的临床案例
5. Pilot Study to Investigate the Role of Somatic Mutations and Clonal Thrombopoiesis in Immune Thrombocytopenic Purpura [D] . Ibrahimi, Sami. 2018

机译：试点研究，探讨体细胞突变和克隆血栓血小杂体在免疫血小板减少紫癜中的作用
6. Atypical manifestations of coronavirus disease 2019 (COVID‐19)–associated autoimmune thrombotic thrombocytopenic purpura [O] . Lisa Law, Gwendolyn Ho, Dazhi Cen, 2021

机译：冠状病毒疾病的非典型表现2019（Covid-19） - 分配的自身免疫性血栓形成血小板细胞脓性紫癜
7. Acquired Thrombotic Thrombocytopenic Purpura and Atypical Hemolytic Uremic Syndrome Successfully Treated with Eculizumab [O] . Appalanaidu Sasapu, Michele Cottler-Fox, Pooja Motwani 2017

机译：获得血栓形成血小板减少紫癜和非典型溶血性血管综合征成功用生态治疗
8. Thrombotic Thrombocytopenic Purpura (TTP): Like Illness Associated with Intravenous Opana ER Abuse: Tennessee, 2012. Morbidity and Mortality Weekly Report, Volume 62, Number 1. [R] . 2013

机译：血栓性血小板减少性紫癜（TTp）：与静脉注射Opana ER滥用相关的疾病：田纳西州，2012年。发病率和死亡率每周报告，第62卷，第1期。

An Atypical Case of Thrombotic Thrombocytopenic Purpura

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