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复发性产后甲状腺炎后肾上腺功能不全(产后施密特综合征):一例报告

Adrenal insufficiency after recurrent post-partum thyroiditis (post-partum Schmidt syndrome): a case report.

作者信息

Mehta H, Badenhoop K, Walfish P G

机构信息

Department of Internal Medicine, University of Toronto Medical School, Ontario, Canada.

出版信息

Thyroid. 1998 Mar;8(3):269-72. doi: 10.1089/thy.1998.8.269.

Abstract

Polyglandular autoimmune syndrome (PGAS) type 2 (Schmidt syndrome) is characterized by the association of primary adrenocortical insufficiency with autoimmune thyroid disease, and/or insulin-dependent diabetes mellitus (IDDM). In this report we describe the occurrence of two episodes of post-partum thyroiditis (PPT) after a first and second pregnancy as well the development acutely of adrenal insufficiency after a second pregnancy. A family history of autoimmune thyroid disease and IDDM as well as positive antiadrenal and antithyroid antibodies and HLA typing is evidence for an underlying polyendocrine autoimmune syndrome. This case report provides further evidence that the immune system that is suppressed in pregnancy to tolerate the fetal allograft can rebound post-partum to unmask polyendocrine autoimmune disorders such as adrenalitis and PPT in susceptible women.

摘要

2型多腺体自身免疫综合征(PGAS,即施密特综合征)的特征是原发性肾上腺皮质功能不全与自身免疫性甲状腺疾病和/或胰岛素依赖型糖尿病(IDDM)并存。在本报告中,我们描述了一名患者在首次和第二次怀孕后发生两次产后甲状腺炎(PPT),以及在第二次怀孕后急性发生肾上腺功能不全。自身免疫性甲状腺疾病和IDDM的家族史,以及抗肾上腺和抗甲状腺抗体阳性及HLA分型,是潜在多内分泌自身免疫综合征的证据。本病例报告进一步证明,孕期为耐受胎儿异体移植物而受到抑制的免疫系统在产后可能会反弹,从而使易感女性出现多内分泌自身免疫性疾病,如肾上腺炎和PPT。

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