Colantonio Mark A, Hartzell Michelle, Shannon Brooke, Iyer Apoorva
Department of Medicine, West Virginia University, Morgantown, USA.
Department of Medicine, Division of Endocrinology, Morgantown, USA.
Eur J Case Rep Intern Med. 2024 May 27;11(6):004627. doi: 10.12890/2024_004627. eCollection 2024.
Addison's disease is a rare, autoimmune condition leading to destruction of the adrenal gland. Autoimmune conditions are known to commonly co-occur. When Addison's disease presents in the setting of autoimmune thyroid disease and/or type 1 diabetes, this condition is termed autoimmune polyendocrine syndrome type II, a rare endocrinopathy found in roughly 1.4-4.5 per 100,000 individuals. Here, we describe a clinical case presenting with hypotension refractory to fluid resuscitation and electrolyte derangements later diagnosed as autoimmune polyendocrine syndrome type II.
Primary adrenal insufficiency may present clinically as shock refractory to fluid resuscitation.Autoimmune polyglandular syndrome type 2 is a rare autoimmune condition occurring in 1.5-4.5 per 100,000 individuals.The presence of an underlying autoimmune condition should raise suspicion for multiple concurrent autoimmune conditions.
艾迪生病是一种罕见的自身免疫性疾病,会导致肾上腺遭到破坏。已知自身免疫性疾病常常同时出现。当艾迪生病在自身免疫性甲状腺疾病和/或1型糖尿病的背景下出现时,这种情况被称为自身免疫性多内分泌腺综合征II型,这是一种罕见的内分泌病,每10万人中约有1.4 - 4.5人患病。在此,我们描述了一例临床病例,该病例出现对液体复苏无反应的低血压和电解质紊乱,后来被诊断为自身免疫性多内分泌腺综合征II型。
原发性肾上腺功能不全在临床上可能表现为对液体复苏无反应的休克。自身免疫性多内分泌腺综合征2型是一种罕见的自身免疫性疾病,每10万人中有1.5 - 4.5人患病。存在潜在的自身免疫性疾病应引发对多种并发自身免疫性疾病的怀疑。