先天性肾上腺增生症成人罕见的肾上腺休止期肿瘤和大量肾上腺肿大,模仿多形性肉瘤转移。

IF 2.8 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Pierluigi Mazzeo, Irene Tizianel, Francesca Galuppini, Marta Sbaraglia, Mattia Barbot
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引用次数: 0

摘要

背景:先天性肾上腺皮质增生症(CAH)是一种常染色体隐性遗传疾病,其特点是由于类固醇合成过程中的酶缺陷导致皮质醇水平受损。在患有 CAH 的成年男性患者中,与疾病控制不佳有关的一种常见并发症是在睾丸中出现异位肾上腺皮质组织,即睾丸肾上腺休息瘤(TART)。相反,女性的卵巢肾上腺休止期肿瘤(OART)极为罕见,而性腺以外部位的肾上腺休止期肿瘤也非常罕见,文献中仅有极少数描述:我们报告了一例未经治疗的 CAH 男性患者,其肿瘤学病史为多形性肉瘤,表现为双侧肾上腺肿大以及腰周和脐周部位的肾上腺憩室瘤,与肉瘤转移相似:结论:对于患有 CAH 且长期未接受治疗的患者,即使肾上腺肿大和异位肾上腺憩室肿瘤在性腺以外的其他部位出现的情况并不常见,也应予以怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uncommon adrenal rest tumors and massive adrenal enlargement in adult with congenital adrenal hyperplasia mimicking metastasis from pleomorphic sarcoma.

Background: Congenital adrenal hyperplasia (CAH) encompassed a bunch of autosomal recessive disorders characterized by impaired cortisol levels due to an enzymatic deficiency in steroid synthesis. In adult male patients with CAH, a frequent complication related to poor disease control is the development of ectopic adrenocortical tissue in the testes, named testicular adrenal rest tumors (TART). Conversely, ovarian adrenal rest tumors (OART) in females are extremely rare and adrenal rests in sites other than gonads are so uncommon to have been described only few times in literature.

Case presentation: We report a case of a male patient with untreated CAH and oncologic history of pleomorphic sarcoma who presented with massive bilateral adrenal enlargement and adrenal rest tumors in peri-lumbar and peri-cecal sites, which mimicked metastasis from sarcoma.

Conclusions: The development of massive adrenal enlargement and ectopic adrenal rest tumors in sites other than gonads, even if very uncommon, should be suspected in patients with CAH and prolonged periods of undertreatment.

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来源期刊
BMC Endocrine Disorders
BMC Endocrine Disorders ENDOCRINOLOGY & METABOLISM-
CiteScore
4.40
自引率
0.00%
发文量
280
审稿时长
>12 weeks
期刊介绍: BMC Endocrine Disorders is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of endocrine disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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