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血栓性血小板减少性紫癜与格雷夫斯病。

Thrombotic thrombocytopenic purpura and Graves disease.

作者信息

Chaar Bassem T, Kudva Ganesh C, Olsen Thomas J, Silverberg Alan B, Grossman Brenda J

机构信息

Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, Missouri 63110, USA.

出版信息

Am J Med Sci. 2007 Aug;334(2):133-5. doi: 10.1097/MAJ.0b013e31812e9735.

Abstract

Patients with an autoimmune disease have a propensity for development of a second autoimmune disease. We report the first instance of a patient with both idiopathic thrombotic thrombocytopenic purpura (TTP) and Graves disease. The TTP remitted with a combination of plasmapheresis and prednisone. Methimazole led to sustained remission of the hyperthyroid state within 6 weeks. Although hyperthyroidism may induce immune imbalance causing autoimmunity, it is unclear if this influenced the development of TTP in our patient and if treatment of hyperthyroidism alone could have resulted in the cure of both diseases.

摘要

患有自身免疫性疾病的患者有患第二种自身免疫性疾病的倾向。我们报告了首例同时患有特发性血栓性血小板减少性紫癜(TTP)和格雷夫斯病的患者。TTP通过血浆置换和泼尼松联合治疗得以缓解。甲巯咪唑在6周内使甲状腺功能亢进状态持续缓解。虽然甲状腺功能亢进可能会导致免疫失衡从而引发自身免疫,但尚不清楚这是否影响了我们这位患者TTP的发病,以及仅对甲状腺功能亢进进行治疗是否能治愈这两种疾病。

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