三睾丸症:一种罕见的泌尿生殖系统异常。

Trupti Tonape, Gurjit Singh, P Koushik, Trinath Tumepalli
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引用次数: 7

摘要

多睾丸症是一种极其罕见的先天性异常,指的是存在两个以上的睾丸。在2岁的儿童中很少有三睾丸症的报道。多子女症通常是偶然发现的。与多囊症相关的最常见异常是腹股沟疝(30%)、睾丸下降症(15%至30%)、睾丸扭转(13%)和鞘膜积液(9%)。一个两岁的孩子带来了双侧睾丸隐睾正常里程碑。阴囊及腹部超声检查显示两睾丸均位于腹股沟管内。术中左侧有2个睾丸,属于Leung III类,右侧有1个睾丸。多子女症的治疗仍然存在争议。多囊症的处理取决于睾丸引流系统的位置、大小和解剖组织以及患者的年龄。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Triorchidism: a rare genitourinary abnormality.

Triorchidism: a rare genitourinary abnormality.

Triorchidism: a rare genitourinary abnormality.

Triorchidism: a rare genitourinary abnormality.

Polyorchidism is an extremely rare congenital anomaly which refers to the presence of more than two testicles. There are very few reports of triorchidism in a 2 year old child. Polyorchidism is usually discovered incidentally. The most common anomalies associated with polyorchidism are inguinal hernia (30%), maldescended testis (15% to 30%), testicular torsion (13%) and hydrocele (9%). A 2-year-old child was brought with bilateral undescended testis with normal milestones. Ultrasonography of scrotum and abdomen showed both the testes to be in inguinal canal. Intra-operatively, on left side - there were two testes, which belonged to Leung III class and one testis on right side. Management of polyorchidism is still controversial. The management of polyorchidism will depend upon the location, size and anatomical organisation of the testicular drainage system and the age of the patient.

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