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分泌促肾上腺皮质激素的类癌肿瘤在库欣综合征出现12年后得以确诊并接受治疗。

Adrenocorticotropin-secreting carcinoid tumour identified and treated 12 years after presentation with Cushing's syndrome.

作者信息

Vaidya B, Richardson D, Hilton C J, Kendall-Taylor P

机构信息

Department of Medicine (Endocrinology), Royal Victoria Infirmary, Newcastle upon Tyne, UK.

出版信息

Postgrad Med J. 1997 Nov;73(865):737-9. doi: 10.1136/pgmj.73.865.737.

Abstract

A case of Cushing's syndrome due to an adrenocorticotropin (ACTH) secreting bronchial carcinoid tumour is described. Endocrine assessment suggested ectopic ACTH syndrome, but imaging revealed no tumour. Bilateral adrenalectomy was performed, and computed tomographic scans of chest and abdomen were performed annually. A small nodule became apparent in the right lung 12 years after the presentation, which postoperatively was confirmed as the bronchial carcinoid tumour responsible for the ectopic ACTH syndrome.

摘要

本文描述了一例因分泌促肾上腺皮质激素(ACTH)的支气管类癌肿瘤导致的库欣综合征病例。内分泌评估提示异位ACTH综合征,但影像学检查未发现肿瘤。遂行双侧肾上腺切除术,并每年进行胸部和腹部的计算机断层扫描。就诊12年后,右肺出现一个小结节,术后证实为导致异位ACTH综合征的支气管类癌肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ec/2431578/4d07de8be3cb/postmedj00155-0052-a.jpg

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