Urachal Tumor: A Case Report of an Extremely Rare Carcinoma

The urachus is a tubular structure that connects the bladder to the allantois in the embryonic development, involuting after the third trimester. The urachus carcinoma is an extremely rare tumor that accounts for <1% of all bladder cancers. We report a case of a 46-year-old woman, with no past me...

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Main Authors: José Palla Garcia, Rita Sampaio, Carlos Peixoto
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Case Reports in Pathology
Online Access:http://dx.doi.org/10.1155/2017/1942595
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author José Palla Garcia
Rita Sampaio
Carlos Peixoto
author_facet José Palla Garcia
Rita Sampaio
Carlos Peixoto
author_sort José Palla Garcia
collection DOAJ
description The urachus is a tubular structure that connects the bladder to the allantois in the embryonic development, involuting after the third trimester. The urachus carcinoma is an extremely rare tumor that accounts for <1% of all bladder cancers. We report a case of a 46-year-old woman, with no past medical history, complaining of hematuria with 6-month duration and a physical exam and an abdominal computed topographic scan revealing an exophytic mass of 6.8 cm longer axis that grew depending on the anterior bladder wall, invading the anterior abdominal wall. Cystoscopy detected mucosal erosion. The biopsy showed structures of adenocarcinoma of enteric type. The surgical specimen showed urachus adenocarcinoma of enteric type with stage IVA in the Sheldon system and stage III in the Mayo system. This case has a 3-year follow-up without disease recurrence.
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spelling doaj-art-8947326a90fe425eb58d9bb68361e0de2025-02-03T01:09:44ZengWileyCase Reports in Pathology2090-67812090-679X2017-01-01201710.1155/2017/19425951942595Urachal Tumor: A Case Report of an Extremely Rare CarcinomaJosé Palla Garcia0Rita Sampaio1Carlos Peixoto2Department of Pathology, Pathological Anatomy Service, Centro Hospitalar do Porto, Largo Professor Abel Salazar, 4099-003 Porto, PortugalDepartment of Pathology, Pathological Anatomy Service, Centro Hospitalar do Porto, Largo Professor Abel Salazar, 4099-003 Porto, PortugalDepartment of Pathology, Pathological Anatomy Service, Centro Hospitalar do Porto, Largo Professor Abel Salazar, 4099-003 Porto, PortugalThe urachus is a tubular structure that connects the bladder to the allantois in the embryonic development, involuting after the third trimester. The urachus carcinoma is an extremely rare tumor that accounts for <1% of all bladder cancers. We report a case of a 46-year-old woman, with no past medical history, complaining of hematuria with 6-month duration and a physical exam and an abdominal computed topographic scan revealing an exophytic mass of 6.8 cm longer axis that grew depending on the anterior bladder wall, invading the anterior abdominal wall. Cystoscopy detected mucosal erosion. The biopsy showed structures of adenocarcinoma of enteric type. The surgical specimen showed urachus adenocarcinoma of enteric type with stage IVA in the Sheldon system and stage III in the Mayo system. This case has a 3-year follow-up without disease recurrence.http://dx.doi.org/10.1155/2017/1942595
spellingShingle José Palla Garcia
Rita Sampaio
Carlos Peixoto
Urachal Tumor: A Case Report of an Extremely Rare Carcinoma
Case Reports in Pathology
title Urachal Tumor: A Case Report of an Extremely Rare Carcinoma
title_full Urachal Tumor: A Case Report of an Extremely Rare Carcinoma
title_fullStr Urachal Tumor: A Case Report of an Extremely Rare Carcinoma
title_full_unstemmed Urachal Tumor: A Case Report of an Extremely Rare Carcinoma
title_short Urachal Tumor: A Case Report of an Extremely Rare Carcinoma
title_sort urachal tumor a case report of an extremely rare carcinoma
url http://dx.doi.org/10.1155/2017/1942595
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