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儿童促性腺激素细胞性腺皮质瘤 1 例报告。

Virilizing adrenocortical oncocytoma in a child: a case report.

机构信息

Department of Pediatrics, Hanyang University College of Medicine, Seoul, Korea.

出版信息

J Korean Med Sci. 2010 Jul;25(7):1077-9. doi: 10.3346/jkms.2010.25.7.1077. Epub 2010 Jun 17.

Abstract

Functioning adrenocortical oncocytomas are extremely rare and most reported patients are 40-60 yr of age. To our knowledge, only 2 cases of functioning adrenocortical oncocytomas have been reported in childhood. We report a case of functioning adrenocortical oncocytoma in a 14-yr-old female child presenting with virilization. She presented with deepening of the voice and excessive hair growth, and elevation of plasma testosterone and dehydroepiandrosterone sulfate. She had an adrenalectomy. The completely resected tumor composed predominantly of oncocytes without atypical mitosis and necrosis. A discussion of this case and a review of the literature on this entity are presented.

摘要

功能性肾上腺皮质嗜酸细胞瘤极为罕见,大多数报道的患者年龄在 40-60 岁之间。据我们所知,仅有 2 例儿童功能性肾上腺皮质嗜酸细胞瘤的病例报告。我们报告了一例 14 岁女性功能性肾上腺皮质嗜酸细胞瘤病例,表现为男性化。她表现为嗓音加深和过度毛发生长,以及血浆睾酮和硫酸脱氢表雄酮升高。她接受了肾上腺切除术。完全切除的肿瘤主要由嗜酸细胞瘤组成,没有非典型有丝分裂和坏死。本文讨论了该病例,并对该实体的文献进行了回顾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4a7/2890887/5e91e46f87a8/jkms-25-1077-g001.jpg

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