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先天性疝的一个惊人发现:完全性脾性腺融合带。

A surprising content of congenital hernia: complete splenogonadal fusion band.

作者信息

Lakshmanan Prakash Manikka, Reddy Ajit Kumar, Nutakki Aditya

机构信息

Department of Radiology, Mahatma Gandhi Medical College & Research Institute, Pondicherry, India.

出版信息

BMJ Case Rep. 2014 Mar 26;2014:bcr2014203640. doi: 10.1136/bcr-2014-203640.

Abstract

Splenogonadal fusion is a rare congenital anomaly. We present the case of a 6-year-old boy who presented with a left inguinoscrotal swelling. With a clinical diagnosis of left congenital inguinal hernia the patient was taken up for explorative laparotomy where a transperitoneal band was noted adherent to the left testis. Biopsy revealed normal splenic tissue. Postoperatively the boy was imaged and a diagnosis of splenogonadal fusion was made. This article illustrates the imaging features of this rare anomaly.

摘要

脾性腺融合是一种罕见的先天性异常。我们报告一例6岁男孩,其表现为左侧腹股沟阴囊肿胀。临床诊断为左侧先天性腹股沟疝,该患者接受了剖腹探查术,术中发现一条经腹膜的索带附着于左侧睾丸。活检显示为正常脾组织。术后对该男孩进行了影像学检查,确诊为脾性腺融合。本文阐述了这种罕见异常的影像学特征。

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