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一例罕见的促肾上腺皮质激素(ACTH)非依赖性大肾上腺增生病例,显示ACTH异位分泌。

A rare case of adrenocorticotropic hormone (ACTH)-independent macroadrenal hyperplasia showing ectopic production of ACTH.

作者信息

Iwata Minoru, Oki Yutaka, Okazawa Teruyo, Ishizawa Shin, Taka Chihiro, Yamazaki Katsuya, Tobe Kazuyuki, Fukuoka Junya, Sasano Hironobu, Nishikawa Tetsuo

机构信息

The First Department of Internal Medicine, Faculty of Medicine, University of Toyama, Japan.

出版信息

Intern Med. 2012;51(16):2181-7. doi: 10.2169/internalmedicine.51.7547. Epub 2012 Aug 15.

Abstract

A 57-year-old Japanese man presented with drug-resistant hypertension without Cushingoid features. Endocrinological tests revealed autonomous secretion of cortisol with suppressed plasma adrenocorticotropic hormone (ACTH). Imaging examinations showed multiple macronodules in the bilateral adrenal gland. These findings were consistent with subclinical Cushing's syndrome caused by ACTH-independent macronodular adrenal hyperplasia (AIMAH). Left adrenalectomy was performed and the resected adrenal lesion was consistent with the pathological diagnosis of AIMAH. Furthermore, in resected tissue, we demonstrated intraadrenal production of ACTH by immunohistochemical analysis and RIA. This is a very rare case of AIMAH showing ectopic production of ACTH, which may be associated with autonomous cortisol secretion.

摘要

一名57岁的日本男性,患有耐药性高血压,无库欣样特征。内分泌检查显示皮质醇自主分泌,同时血浆促肾上腺皮质激素(ACTH)受到抑制。影像学检查显示双侧肾上腺有多个大结节。这些发现符合由ACTH非依赖性大结节性肾上腺增生(AIMAH)引起的亚临床库欣综合征。实施了左侧肾上腺切除术,切除的肾上腺病变与AIMAH的病理诊断相符。此外,在切除组织中,我们通过免疫组织化学分析和放射免疫分析证实了肾上腺内有ACTH产生。这是一例极为罕见的AIMAH病例,显示ACTH异位产生,这可能与皮质醇自主分泌有关。

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