Banzal Subodh, Singhai Abhishek
Department of Medicine, Sri Aurobindo Medical College, Indore, Madhya Pradesh, India.
Indian J Crit Care Med. 2014 May;18(5):326-7. doi: 10.4103/0972-5229.132507.
Autoimmune polyendocrine syndrome Type II (APS II), also known as polyglandular autoimmune syndrome Type II or Schmidt syndrome, is constellations of multiple endocrine gland insufficiencies. It is a rare, but most common of the immunoendocrinopathy syndrome. It is characterized by the obligatory occurrence of autoimmune Addison's disease in combination with thyroid autoimmune diseases and/or Type I diabetes, hypogonadism, hypophysitis, myasthenia gravis, vitiligo, alopecia, pernicious anemia, and celiac disease. Here, we report a case of 38-year-old female patient presented with shock, further diagnosed to have APS II.
自身免疫性多内分泌腺综合征II型（APS II），也称为多腺体自身免疫综合征II型或施密特综合征，是多种内分泌腺功能不全的组合。它是一种罕见但最常见的免疫内分泌病综合征。其特征是自身免疫性艾迪生病必然与甲状腺自身免疫性疾病和/或I型糖尿病、性腺功能减退、垂体炎、重症肌无力、白癜风、脱发、恶性贫血和乳糜泻同时出现。在此，我们报告一例38岁女性患者，出现休克，进一步诊断为APS II。
