藏于先天性左肺发育不全的促肾上腺皮质激素肿瘤

IF 1.6 4区医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS

Interactive cardiovascular and thoracic surgery Pub Date : 2022-05-16 DOI:10.1093/icvts/ivac130

Xueyu Chen, Yajie Zhang, Jules Lin, Hecheng Li

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引用次数: 0

摘要

由于难以定位隐匿性促肾上腺皮质激素(ACTH)肿瘤，异位促肾上腺皮质激素(ACTH)综合征一直是治疗上的挑战。在这里，我们报告一例67岁的女性异位ACTH综合征和ACTH分泌肿瘤隐藏在先天性左肺发育不全。本例患者行左侧全肺切除术后取得满意的治疗效果。

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An ACTH-secreting tumour hidden in a congenitally hypoplastic left lung

Abstract Ectopic adrenocorticotrophic hormone (ACTH) syndrome has historically been a therapeutic challenge because of the difficulty localizing occult ACTH-secreting tumours. Here, we report a case of a 67-year-old woman with ectopic ACTH syndrome and had an ACTH-secreting tumour hidden within a congenitally hypoplastic left lung. A satisfactory therapeutic outcome was obtained after left pneumonectomy was performed on patient in this case.

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来源期刊

Interactive cardiovascular and thoracic surgery CARDIAC & CARDIOVASCULAR SYSTEMS-

CiteScore

3.30

自引率

0.00%

发文量

292

审稿时长

2-4 weeks

期刊介绍： Interactive CardioVascular and Thoracic Surgery (ICVTS) publishes scientific contributions in the field of cardiovascular and thoracic surgery, covering all aspects of surgery of the heart, vessels and the chest. The journal publishes a range of article types including: Best Evidence Topics; Brief Communications; Case Reports; Original Articles; State-of-the-Art; Work in Progress Report.