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表现为垂体瘤的原发性甲状腺功能减退症。

Primary thyroid failure presenting as a pituitary tumour.

作者信息

Daggett P, Harsoulis P, Kuku S F, Pearse E, Fraser T R

出版信息

Postgrad Med J. 1975 Feb;51(592):85-9. doi: 10.1136/pgmj.51.592.85.

Abstract

A 20-year-old female was referred as a pituitary tumour with failure to grow. Primary hypothyroidism from the age of 8 had been diagnosed at the age of 11, when the patient was put on thyroid replacement therapy. Routine investigations showed normal anterior pituitary function, and confirmed the diagnosis of primary hypothyroidism. A needle biopsy of the pituitary gland revealed an empty fossa. The possible relation of the empty sella with the primary hypothyroidism is discussed. A chromosome anomaly, deletion of the short arm of an X chromosome, was found and its contribution to the delayed growth is discussed.

摘要

一名20岁女性因垂体肿瘤伴生长发育迟缓前来就诊。患者自8岁起出现原发性甲状腺功能减退,11岁时确诊,随后开始接受甲状腺替代治疗。常规检查显示垂体前叶功能正常,确诊为原发性甲状腺功能减退。垂体针吸活检显示蝶鞍空泡。本文讨论了空蝶鞍与原发性甲状腺功能减退之间可能存在的关系。此外,还发现了一种染色体异常,即X染色体短臂缺失,并探讨了其对生长发育迟缓的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536b/2495715/c72116dd8896/postmedj00290-0040-a.jpg

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