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The Role of Multidisciplinary Diagnosis in Managing a Rare Case Report of Congenital Urachal Fistula Complicated by Sertoli-Leydig Cell Tumor and Male Pseudohermaphroditism

2026-06-05

Abstract excerpt

<title>Abstract</title> <p>Background The concurrent occurrence of congenital urachal fistula, Sertoli-Leydig cell tumor, and male pseudohermaphroditism is exceptionally rare, with no similar case reported to date..Congenital urachal fistula is a rare embryological remnant resulting from incomplete closure of the urachus, presenting inflammation of the umbilicus and purulent discharge. Sertoli-Leydig cell tumor...

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Literature Corpus work
9d3707c6-5b86-5280-acf2-d7ff562a2be9
DOI
10.21203/rs.3.rs-9527556/v1
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The Role of Multidisciplinary Diagnosis in Managing a Rare Case Report of Congenital Urachal Fistula Complicated by Sertoli-Leydig Cell Tumor and Male PseudohermaphroditismDOI 10.21203/rs.3.rs-9527556/v1
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