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一例伴有原发性闭经的多发性内分泌腺瘤病

A case of multiple endocrine adenomatosis with primary amenorrhoea.

作者信息

Vandeweghe M, Braxel K, Schutyser J, Vermeulen A

出版信息

Postgrad Med J. 1978 Sep;54(635):618-22. doi: 10.1136/pgmj.54.635.618.

Abstract

A well documented sporadic case of multiple endocrine adenomatosis (MEA) type I, with the pituitary tumour presenting as a prolactinoma, is described in a 28-year-old female. Primary amenorrhoea, resulting from hyperprolactinaemia, was the first symptom of the polyglandular neoplasia. A gastrinoma was removed from the head of the pancreas and latent hyperparathyroidism appeared to be present. Treatment with bromocriptine was poorly tolerated; neurosurgical intervention was refused by the patient. The possibility that a serum prolactin determination may be useful in detecting pituitary involvement in MEA deserves consideration.

摘要

本文描述了一例记录详尽的散发型I型多发性内分泌腺瘤病(MEA),患者为一名28岁女性,垂体肿瘤表现为催乳素瘤。高催乳素血症导致的原发性闭经是这种多腺体肿瘤形成的首发症状。从胰头切除了胃泌素瘤,且似乎存在潜在的甲状旁腺功能亢进。患者对溴隐亭治疗耐受性差;患者拒绝了神经外科干预。血清催乳素测定可能有助于检测MEA患者的垂体受累情况,这一可能性值得考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3584/2425223/730793a333c6/postmedj00261-0043-a.jpg

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