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孤立性获得性 ACTH 缺乏症与原发性甲状腺功能减退症:短篇系列报道与文献复习

Isolated acquired ACTH deficiency and primary hypothyroidism: a short series and review.

机构信息

Department of Endocrinology and Metabolism, Cork University Hospital, Wilton, Cork, Ireland.

出版信息

Pituitary. 2011 Dec;14(4):358-61. doi: 10.1007/s11102-008-0164-9.

Abstract

Idiopathic isolated ACTH deficiency, congenital or acquired, is rare. It may be found in association with primary hypothyroidism. Here we describe four cases of acquired idiopathic isolated ACTH deficiency illustrating its importance and variable presentation. All cases had a structurally normal pituitary gland and persistently normal residual pituitary function. Three cases had co-existing primary hypothyroidism. We discuss the protean presentation of this rare but important condition, its treatment, associations, and possible aetiologies.

摘要

特发性孤立性 ACTH 缺乏症,先天性或获得性,较为罕见。它可能与原发性甲状腺功能减退症同时发生。本文描述了 4 例获得性特发性孤立性 ACTH 缺乏症病例,阐明了其重要性和多变的表现。所有病例的垂体结构均正常,且残留垂体功能持续正常。3 例伴有原发性甲状腺功能减退症。我们讨论了这种罕见但重要疾病的多种表现形式、治疗方法、相关因素和可能的病因。

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