Devoto E, Aravena L, Corvalan L, Lioi X, Munizaga F, Soto N, Hidalgo S, Barrera R, Gajardo H
Departamento de Endocrinología, Hospital Paula Jaraquemada, Universidad de Chile, Santiago.
Rev Med Chil. 1990 Jun;118(6):635-42.
The autoimmune polyglandular syndrome is characterized by the association of 2 or more endocrine disorders of autoimmune origin which may coexist with autoimmune disorders in other organs. Roughly 25% of patients with an autoimmune endocrinopathy show evidence of autoimmune disease elsewhere. We report 21 patients with autoimmune polyglandular syndrome classified according to Neufeld.
自身免疫性多内分泌腺综合征的特征是2种或更多种自身免疫性起源的内分泌疾病相关联,这些疾病可能与其他器官的自身免疫性疾病共存。大约25%的自身免疫性内分泌病患者在其他部位有自身免疫性疾病的证据。我们报告了21例根据诺伊费尔德分类的自身免疫性多内分泌腺综合征患者。