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一名儿童的原发性甲状腺功能减退症酷似垂体大腺瘤。

Primary hypothyroidism in a child mimicking a pituitary macroadenoma.

作者信息

Hopper N W, Albanese A

机构信息

Department of Paediatric Endocrinology, St. George's Hospital, London SW17 0QT, UK.

出版信息

Horm Res. 2005;63(2):61-4. doi: 10.1159/000083568. Epub 2005 Jan 24.

Abstract

We report the case of an 11-year-old girl with primary autoimmune hypothyroidism causing secondary pituitary enlargement. She presented with headaches and a pituitary mass on MRI thought to be due to a pituitary macroadenoma. Resolution of the pituitary mass and symptoms occurred with thyroxine therapy. It is mandatory to rule out primary hypothyroidism as a cause of pituitary enlargement before surgery is considered.

摘要

我们报告了一例11岁原发性自身免疫性甲状腺功能减退导致继发性垂体增大的女孩病例。她因头痛就诊,磁共振成像(MRI)显示垂体肿块,最初认为是垂体大腺瘤所致。甲状腺素治疗后垂体肿块及症状消失。在考虑手术前,必须排除原发性甲状腺功能减退作为垂体增大的病因。

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