A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report

A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic ure...

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Detalles Bibliográficos
Autores principales: Yamaçake, Kleiton Gabriel Ribeiro, Giron, Amilcar Martins, Tannuri, Uenis, Srougi, Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Israelita de Ensino e Pesquisa Albert Einstein 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891169/
https://www.ncbi.nlm.nih.gov/pubmed/25003932
http://dx.doi.org/10.1590/S1679-45082014RC2746
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author Yamaçake, Kleiton Gabriel Ribeiro
Giron, Amilcar Martins
Tannuri, Uenis
Srougi, Miguel
author_facet Yamaçake, Kleiton Gabriel Ribeiro
Giron, Amilcar Martins
Tannuri, Uenis
Srougi, Miguel
author_sort Yamaçake, Kleiton Gabriel Ribeiro
collection PubMed
description A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic urethra, criptorquidy bilateral with nonpalpable testis and imperforate anus. A colostomy was constructed immediately after birth. The child underwent excision of perineal mass, bilateral orchidopexy, Duplay neourethroplasty and coloanal anastomosis at 3 months of age. The histopathological examination of the perineal mass revealed a hamartoma.
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spelling pubmed-48911692016-08-10 A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report Yamaçake, Kleiton Gabriel Ribeiro Giron, Amilcar Martins Tannuri, Uenis Srougi, Miguel Einstein (Sao Paulo) Case Report A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic urethra, criptorquidy bilateral with nonpalpable testis and imperforate anus. A colostomy was constructed immediately after birth. The child underwent excision of perineal mass, bilateral orchidopexy, Duplay neourethroplasty and coloanal anastomosis at 3 months of age. The histopathological examination of the perineal mass revealed a hamartoma. Instituto Israelita de Ensino e Pesquisa Albert Einstein 2014 /pmc/articles/PMC4891169/ /pubmed/25003932 http://dx.doi.org/10.1590/S1679-45082014RC2746 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yamaçake, Kleiton Gabriel Ribeiro
Giron, Amilcar Martins
Tannuri, Uenis
Srougi, Miguel
A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report
title A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report
title_full A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report
title_fullStr A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report
title_full_unstemmed A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report
title_short A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report
title_sort rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891169/
https://www.ncbi.nlm.nih.gov/pubmed/25003932
http://dx.doi.org/10.1590/S1679-45082014RC2746
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