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一名新生儿右侧睾丸坏死,左侧睾丸未降。

Right testicular necrosis and left vanishing testis in a neonate.

作者信息

Miyata Ichiro, Yoshikawa Hideki, Ikemoto Mamoru, Eto Yoshikatsu

机构信息

Department of Pediatrics, Jikei University School of Medicine, Tokyo, Japan.

出版信息

J Pediatr Endocrinol Metab. 2007 Mar;20(3):449-54. doi: 10.1515/jpem.2007.20.3.449.

Abstract

We describe a rare case of right testicular necrosis and left vanishing testis in a neonate. The patient presented with a right swollen testis and left non-palpable testis at birth. Exploratory laparotomy was performed at 23 days after birth, and the right testis was extirpated because of extensive necrosis due to torsion of the spermatic cord. Histopathological examination revealed a massively necrotic testicular structure with hypertrophy of Leydig cells. Hypergonadotropinemia was also recognized before operation. On laparoscopy at the age of 5.3 years, a normal left vas deferens and spermatic vessels exiting through the internal inguinal ring were confirmed, although the patient's left testis was not found in the intraperitoneal cavity. An hCG test demonstrated no response of serum testosterone. These findings suggested a diagnosis of left vanishing testis due to testicular regression. We therefore speculated that bilateral asynchronous testicular torsion had occurred prenatally in this patient.

摘要

我们描述了一例新生儿罕见的右侧睾丸坏死及左侧睾丸消失的病例。该患者出生时右侧睾丸肿大,左侧睾丸无法触及。出生23天后进行了剖腹探查术,右侧睾丸因精索扭转导致广泛坏死而被切除。组织病理学检查显示睾丸结构大量坏死,伴有Leydig细胞肥大。术前还发现了高促性腺激素血症。在5.3岁时进行腹腔镜检查,尽管在腹腔内未发现患者的左侧睾丸,但确认了正常的左侧输精管和通过腹股沟内环穿出的精索血管。人绒毛膜促性腺激素(hCG)试验显示血清睾酮无反应。这些发现提示诊断为左侧睾丸因睾丸退化而消失。因此,我们推测该患者在产前发生了双侧异步睾丸扭转。

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