Hoffman W H, England B G, Gomez L M, Rosculet G, Gala R R
Neuropediatrics. 1987 Feb;18(1):37-9. doi: 10.1055/s-2008-1052432.
A child diagnosed with long-standing primary hypothyroidism at age 10 and subsequent pseudotumor cerebri after initiation of thyroid therapy developed an empty sella and inappropriate thyrotropin secretion. No other evidence of thyroid hormone resistance was evident nor was there evidence of other endocrine dysfunction. This case confirms previous reports of a relationship between autoimmune thyroid disease, pseudotumor cerebri, empty sella and inappropriate anterior pituitary function.
一名10岁时被诊断为长期原发性甲状腺功能减退症的儿童,在开始甲状腺治疗后出现了假性脑瘤,随后出现了空蝶鞍和促甲状腺激素分泌异常。没有其他甲状腺激素抵抗的证据,也没有其他内分泌功能障碍的证据。该病例证实了先前关于自身免疫性甲状腺疾病、假性脑瘤、空蝶鞍和垂体前叶功能异常之间关系的报道。