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难治性血栓性血小板减少性紫癜1例

Management of refractory thrombotic thrombocytopenic purpura:a case report
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摘要 血栓性血小板减少性紫癜(thrombotic thrombocytopenic purpura,TTP)是一种罕见疾病,常累积全身多系统,病情凶险,死亡率高,血浆置换和糖皮质激素常作为TTP的首选治疗措施。难治性TTP是指经5次血浆置换及糖皮质激素治疗后血小板计数仍未见改善。本文报道一例经血浆置换和糖皮质激素治疗后未缓解的难治性TTP患者,使用利妥昔单抗后病情缓解。 Thrombotic thrombocytopenic purpura(TTP)is a rare disease causing a critical condition often involving multisystems and having a high mortality rate.The mainstays of treatment being plasma exchange(PEX)and corticosteroids.Refractory TTP is defined as a failure of platelet response after 5 PEX and corticosteroids therapy.This article reports a patient with refractory TTP who did not improve after a PEX and corticosteroids therapy,but was later successfully treated with rituximab.
作者 张洋 华天凤 郑瑶 肖文艳 杨旻 Yang ZHANG;Tian-Feng HUA;Yao ZHENG;Wen-Yan XIAO;Min YANG(The Second Department of Intensive Care Unit,the Second Affiliated Hospital of Anhui Medical University,Hefei 230601,China;The Laboratory of Cardiopulmonary Resuscitation and Critical Care Medicine,the Second Affiliated Hospital of Anhui Medical University,Hefei 230601,China)
出处 《医学新知》 CAS 2023年第3期237-242,共6页 New Medicine
基金 国家自然科学基金面上项目(82072134)。
关键词 血栓性血小板减少性紫癜 利妥昔单抗 血浆置换 Thrombotic thrombocytopenic purpura Rituximab Plasma exchange
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  • 1Scully M, McDonald V, Cavenagh J, et al. A phase 2 study of the safety and efficacy of rituximab with plasma exchange in acute acquired thrombotic thrombocytopenic purpura[J]. Blood, 2011, 118(7):1746-1753.
  • 2Sadler JE. Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura[J]. Blood, 2008, 112(1):11-18.
  • 3Shumak KH, Rock GA, Nair RC. Late relapses in patients successfully treated for thrombotic thrombocytopenic purpura. Canadian Apheresis Group[J]. Ann Intern Med, 1995, 122(8): 569-572.
  • 4Scully M, Yarranton H, Liesner R, et al. Regional UK TTP registry: correlation with laboratory ADAMTS 13 analysis and clinical features[J]. Br J Haematol, 2008, 142(5):819-826.
  • 5Peyvandi F, Lavoretano S, Palla R, et al. ADAMTS13 andmanti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission[J]. Haematologica, 2008, 93(2): 232-239.
  • 6Kremer Hovinga JA, L?mmle B. Role of ADAMTS13 in the pathogenesis, diagnosis, and treatment of thrombotic thrombocytopenic purpura[J]. Hematology Am Soc Hematol Educ Program, 2012, 2012:610-616.
  • 7Ferrari S, Mudde GC, Rieger M, et al. IgG subclass distribution of anti-ADAMTS13 antibodies in patients with acquired thrombotic thrombocytopenic purpura[J]. J Thromb Haemost, 2009, 7(10): 1703-1710.
  • 8Allford SL, Hunt BJ, Rose P, et al. Guidelines on the diagnosis and management of the thrombotic microangiopathic haemolytic anaemias[J]. Br J Haematol, 2003, 120(4):556-573.
  • 9Blombery P, Scully M. Management of thrombotic thrombocytopenic purpura: current perspectives[J]. J Blood Med, 2014, 5:15-23.
  • 10Crawley JT, Scully MA. Thrombotic thrombocytopenic purpura: basic pathophysiology and therapeutic strategies[J]. Hematology Am Soc Hematol Educ Program, 2013, 2013:292-299.

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