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持续性苗勒管综合征:单侧隐睾的罕见病因。

Persistent Mullerian duct syndrome: a rare cause of unilateral cryptorchidism.

作者信息

Keukens Laura, Zijp Gerda, Mul Dick

机构信息

Pediatrics Department, HAGAziekenhuis/Juliana Children's Hospital, The Hague, Netherlands.

出版信息

BMJ Case Rep. 2012 Sep 12;2012:bcr0220125722. doi: 10.1136/bcr.02.2012.5722.

Abstract

Persistent Mullerian duct syndrome (PMDS) is a rare syndrome and sometimes the cause of a common problem in paediatric and surgical practice, namely undescended testes. PMDS is a recessive disease in which there is a defect in anti-Mullerian hormone secretion or receptor activity resulting in persistence of Mullerian structures such as a uterus or fallopian tubes with otherwise normal virilisation. Here the authors present a case of a 1½-year-old boy who was referred to their hospital because of unilateral cryptorchidism. During laparoscopic surgery, two gonads were present joined together by a uterus-like structure. Additional investigations showed a normal male karyotype and biopsies of the gonads revealed infantile testis parenchyma making the diagnosis PMDS likely.

摘要

持续性苗勒管综合征(PMDS)是一种罕见的综合征,有时是儿科和外科临床中常见问题(即隐睾)的病因。PMDS是一种隐性疾病,其抗苗勒管激素分泌或受体活性存在缺陷,导致苗勒管结构(如子宫或输卵管)持续存在,而男性化过程在其他方面正常。本文作者报告了一例1.5岁男孩因单侧隐睾转诊至他们医院的病例。在腹腔镜手术中,发现两个性腺通过一个类似子宫的结构连接在一起。进一步检查显示男性核型正常,性腺活检显示为婴儿型睾丸实质,这使得PMDS的诊断很有可能。

相似文献

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Persistent Mullerian Duct Syndrome associated with transverse testicular ectopia: a case report.
Eur J Pediatr Surg. 1997 Feb;7(1):60-2. doi: 10.1055/s-2008-1071055.

本文引用的文献

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A visual pitfall: persistent Müllerian duct syndrome (PMDS).一个视觉陷阱:持续性苗勒管综合征(PMDS)。
Acta Paediatr. 2008 Jan;97(1):129-32. doi: 10.1111/j.1651-2227.2007.00573.x. Epub 2007 Dec 3.
9
Anti-Müllerian hormone receptor defect.抗苗勒管激素受体缺陷
Best Pract Res Clin Endocrinol Metab. 2006 Dec;20(4):599-610. doi: 10.1016/j.beem.2006.09.004.

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