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男性子宫切除术?一例罕见病例报告。

Hysterectomy in a male? A rare case report.

作者信息

Sherwani Afak Yusuf, Shah Abdul Qayoom, Wani Abdul Majeed, Bashir Ahmad Chalkoo, Bashir Ahmad Khan, Sofi Farooq Ahmad, Wani Ashfaq Amin, Lone Wasim, Sherwani Ab Hamid, Sheikh Mehmood Rashid, Sharma Raj Reshi

机构信息

Department of General surgery, District Hospital Baramulla, Kashmir, India.

Department of General surgery, District Hospital Baramulla, Kashmir, India.

出版信息

Int J Surg Case Rep. 2014;5(12):1285-7. doi: 10.1016/j.ijscr.2014.10.020. Epub 2014 Oct 30.

Abstract

INTRODUCTION

Persistent Mullerian duct syndrome is a rare form of male pseudo-hermaphroditism characterized by the presence of Mullerian duct structures in an otherwise phenotypically, as well as genotypically, normal man; only a few cases have been reported in the worldwide literature. A great variety of organs have been found in indirect inguinal hernial sacs.

PRESENTATION OF CASE

We report a case of 70 year old man, father of 4 children with unilateral cryptorchidism on the right side and left-sided obstructed inguinal hernia containing uterus and fallopian tube (that is, hernia uteri inguinalis; type I male form of persistent Mullerian duct syndrome) coincidentally detected during an operation for an obstructed left inguinal hernia.

DISCUSSION

PMDS is usually coincidently detected during surgical operation, as was in our case. However pre-operative ultrasonography, computerized tomography and MRI allow possible pre-operative diagnosis.(3) CONCLUSION: In cases of unilateral or bilateral cryptorchidism associated with hernia, as in our patient's case, the possibility of PMDS should be kept in mind.

摘要

引言

持续性苗勒管综合征是男性假两性畸形的一种罕见形式,其特征是在表型和基因型均正常的男性体内存在苗勒管结构;全球文献中仅报道了少数病例。在腹股沟斜疝囊内发现了各种各样的器官。

病例介绍

我们报告一例70岁男性病例,他是4个孩子的父亲,右侧单侧隐睾,左侧腹股沟疝嵌顿,术中意外发现疝内容物为子宫和输卵管(即腹股沟子宫疝;持续性苗勒管综合征的I型男性形式)。

讨论

如我们的病例所示,PMDS通常在手术过程中偶然发现。然而,术前超声、计算机断层扫描和磁共振成像有助于进行术前诊断。结论:在单侧或双侧隐睾合并疝的病例中,如我们患者的情况,应考虑到PMDS的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/700f/4276263/a5d04616b7f7/gr1.jpg

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