Miller M J, Horst T V
Acta Endocrinol (Copenh). 1982 Apr;99(4):573-6. doi: 10.1530/acta.0.0990573.
A patient presented with severe primary hypothyroidism and secondary adrenal insufficiency due to the isolated deficiency of ACTH. The diagnostic evidence suggests that both are of an autoimmune aetiology. Acquired isolated or unitrophic ACTH deficiency is a rare but definite cause of adrenal insufficiency. Additional case reports and autopsy studies describing acquired isolated ACTH deficiency associated with autoimmune thyroid disease have appeared in the literature suggesting that the association is more than coincidental. Combined thyroid and adrenal failure should not always be considered to be the result of combined end organ failure. Unitrophic isolated ACTH deficiency may coexist with primary hypothyroidism.
一名患者因促肾上腺皮质激素(ACTH)单独缺乏而出现严重的原发性甲状腺功能减退和继发性肾上腺功能不全。诊断证据表明两者均为自身免疫病因。获得性孤立性或单一性ACTH缺乏是肾上腺功能不全的一种罕见但明确的病因。文献中出现了更多描述与自身免疫性甲状腺疾病相关的获得性孤立性ACTH缺乏的病例报告和尸检研究,表明这种关联并非偶然。甲状腺和肾上腺联合衰竭不应总是被认为是终末器官联合衰竭的结果。单一性孤立性ACTH缺乏可能与原发性甲状腺功能减退共存。