保守治疗14岁男童腹膜内多角症1例报告及文献复习。

Case Reports in Urology Pub Date : 2025-09-09 eCollection Date: 2025-01-01 DOI:10.1155/criu/5258413
Panagiotis Nikolinakos, Abhisekh Chatterjee, Efstratios Christianakis, Ioannis Alexandrou, Nikolaos Chatzikrachtis, Elisavet Kotsi, Viktor Alargkof, Ivo Donkov, Samuel Bishara, Nikolaos Zavras, Joseph M Norris
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引用次数: 0

摘要

多儿症或多睾丸(snt)是一种罕见的先天性疾病,其管理仍存在争议,特别是在具有其他伴随特征的儿科病例中。我们报告一个14岁男孩的腹囊内多儿症,由于父母的偏好和组织学确认的需要,手术治疗。患者有2周的阴囊无痛性沉重感。体格检查和多普勒超声检查显示一个1.8厘米的肿块融合到左侧睾丸下极,并伴有1级精索静脉曲张、精索积液和睾丸阑尾。虽然最初提供了阴囊MRI,但家庭拒绝支持及时的组织学确认。手术探查证实合并多生睾丸,活检显示精子发生正常;这与A3型三兰花症一致。随访12个月,无并发症或症状复发。本病例强调了在影像不确定或需要组织学证实的情况下,手术探查的应用。家长的关心和长期的保证也可能合理地影响管理决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Conservative Management of Intrascrotal Polyorchidism in a 14-Year-Old Boy: A Case Report and Review of the Current Literature.

Conservative Management of Intrascrotal Polyorchidism in a 14-Year-Old Boy: A Case Report and Review of the Current Literature.

Conservative Management of Intrascrotal Polyorchidism in a 14-Year-Old Boy: A Case Report and Review of the Current Literature.

Polyorchidism, or supernumerary testes (SNTs), is a rare congenital condition, management of which remains debated, particularly in paediatric cases with other concomitant features. We report a case of intrascrotal polyorchidism in a 14-year-old boy managed surgically due to parental preference and the need for histological confirmation. The patient presented with a 2-week history of painless heaviness in the scrotum. Physical examination and Doppler ultrasonography revealed a 1.8 cm mass fused to the inferior pole of the left testicle with associated Grade 1 varicocele, hydrocele and testicular appendix. Although MRI of the scrotum was initially offered, the family declined in favour of timely histological confirmation. Surgical exploration confirmed a fused supernumerary testicle and a biopsy showed normal spermatogenesis; this was consistent with Type A3 triorchidism. The patient had no complications or recurrence of symptoms at 12-month follow-up. This case highlights the use of surgical exploration in selected intrascrotal polyorchidism cases where imaging can be inconclusive or histological confirmation is required. Parental concerns and long-term reassurance may also reasonably influence management decisions.

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