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小儿择期睾丸固定术中偶然发现多睾症:一例报告

Incidental finding of polyorchidism during elective orchidopexy in a child: a case report.

作者信息

Hussain Eiman Yassir Musa, Amedjoudj Khadidja

机构信息

Faculty of Medicine, Elrazi University, Khartoum, Sudan.

Department of Pediatric Surgery, Public Hospital Mohamed Boudiaf, Oum El Bouaghi, Algeria.

出版信息

Urol Case Rep. 2025 Sep 2;63:103197. doi: 10.1016/j.eucr.2025.103197. eCollection 2025 Nov.

DOI:10.1016/j.eucr.2025.103197
PMID:40979513
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12444454/
Abstract

Polyorchidism is a rare congenital anomaly characterized by the presence of more than two testes. It is commonly discovered incidentally during surgical exploration. We report a case of a 7-year-old male with Polyorchidism diagnosed during elective surgery for undescended left testis. An intra-scrotal supernumerary testis was found with a cryptorchidic testis located at the inguinal canal. We opted for Orchidectomy of the intrascrotal atrophic testis, and orchidopexy of the healthy testis. Histopathology confirmed the diagnosis. Postoperative recovery and follow-up were uneventful. This case highlights the importance of polyorchidism management based on anatomical and functional findings intraoperatively.

摘要

多睾症是一种罕见的先天性异常,其特征是存在两个以上的睾丸。它通常在手术探查时偶然发现。我们报告一例7岁男性,在择期手术治疗左侧隐睾时被诊断为多睾症。在阴囊内发现一个额外的睾丸,同时在腹股沟管处有一个隐睾。我们选择切除阴囊内萎缩的睾丸,并对健康的睾丸进行睾丸固定术。组织病理学证实了诊断。术后恢复和随访情况良好。该病例强调了基于术中解剖和功能发现进行多睾症管理的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8489/12444454/b7064f2253f9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8489/12444454/fcf8a52ce157/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8489/12444454/b7064f2253f9/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8489/12444454/fcf8a52ce157/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8489/12444454/b7064f2253f9/gr2.jpg

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本文引用的文献

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Supernumerary Testis (Polyorchidism).额外睾丸(多睾症)。
Balkan Med J. 2025 Mar 3;42(2):168-169. doi: 10.4274/balkanmedj.galenos.2024.2024-10-81. Epub 2025 Jan 13.
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Polyorchidism with testicular hydrocele: A case report.多睾症合并睾丸鞘膜积液:一例报告。
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J Med Case Rep. 2014 Dec 25;8:464. doi: 10.1186/1752-1947-8-464.
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