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以阴囊急症形式表现的卵睾性发育障碍

Ovotesticular Disorder of Sex Development Presenting as a Scrotal Emergency.

作者信息

Zhao Junfeng, Zhu Jianming, Ding Shuxia, Li Haibo

机构信息

Departments of a Pediatrics Surgery.

Pediatric Endocrinology.

出版信息

Pediatrics. 2023 Dec 1;152(6). doi: 10.1542/peds.2023-061810.

Abstract

Ovotesticular (OT) disorder of sex development (DSD) is a rare condition that affects the development of reproductive organs and manifests in a wide range of phenotypic presentations. The clinical diagnosis of this condition is challenging because of its atypical nature, and the variability of presentation in 46,XX OT-DSD cases makes it a complex issue in medical practice. We report a case of a 13-year-old boy who presented with left scrotal pain. Further exploration revealed a tunica rupture without testicular torsion of the left testis, whereas the histopathological analysis of a nodule excised from the right testis indicated the presence of ovotestis tissues. A second nonemergent surgery preserved the testicular tissues as the ovarian tissue in both gonads was excised. After 22 months of follow-up, the patient's testes produced normal testosterone levels sustained over time without any exogenous supplementation. This case reveals that, in male children who present with an acute scrotal disease as adolescents, the gonads should be retained until the etiology is confirmed, and the possibility of OT-DSD should be considered.

摘要

卵睾性性发育障碍(OT-DSD)是一种罕见疾病,影响生殖器官的发育,并表现出广泛的表型特征。由于其非典型性质,这种疾病的临床诊断具有挑战性,而46,XX OT-DSD病例表现的变异性使其成为医学实践中的一个复杂问题。我们报告一例13岁男孩,因左侧阴囊疼痛就诊。进一步检查发现左侧睾丸白膜破裂但无睾丸扭转,而从右侧睾丸切除的一个结节的组织病理学分析显示存在卵睾组织。第二次非急诊手术保留了睾丸组织,因为双侧性腺中的卵巢组织均被切除。经过22个月的随访,患者的睾丸在没有任何外源性补充的情况下,随着时间的推移产生了正常水平的睾酮。该病例表明,对于青春期出现急性阴囊疾病的男性儿童,在病因确诊之前应保留性腺,并应考虑OT-DSD的可能性。

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