Literature DB >> 28684259

Zinner Syndrome: A Diagnostic Challenge. The Aid of Morphology, Embryology, and Immunohistochemistry.

Michela Campora1, Alberto Olivero2, Carlo Toncini3, Bruno Spina3, Ezio Fulcheri4, Carlo Terrone5, Valerio Gaetano Vellone1.   

Abstract

We investigate a patient with right kidney agenesis. Imaging showed the presence of a cystic mass dislocating the bladder. The specimen showed three formations: a kidney remnant, a ureter with blind-ending branch, and a cyst, from which departed another tubular structure, considered the deferential duct. The specimen was sampled. The supposed kidney was formed by cystic structures. Examination of the tubular structures disclosed smooth muscle fibers with no lumen, whereas the cyst was surrounded by fibrous and hemorrhagic walls. Collaboration among specialists allowed the diagnosis of Zinner syndrome, a congenital malformation due to an abnormal development of the Wolffian duct.
Copyright © 2017 Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 28684259     DOI: 10.1016/j.urology.2017.06.013

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  1 in total

1.  Incidental imaging findings suggesting Zinner syndrome in a young patient with pulmonary embolism: A case report.

Authors:  Benedikt Hergan; Franz A Fellner; Kaveh Akbari
Journal:  Radiol Case Rep       Date:  2020-02-19
  1 in total

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