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A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula
Aphallia or penile agenesis is a rare case of the genitourinary system which has an association with upper urinary tract disorder. Failure of fetal genital tubercle formation in the embryonic period is the cause of this disorder. The incidence of aphallia according to previous studies is about 1 in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530489/ https://www.ncbi.nlm.nih.gov/pubmed/36204399 http://dx.doi.org/10.1016/j.radcr.2022.08.107 |
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author | Kian, Behnam Esmaeilian, Saeed Kayedi, Mehrdad |
author_facet | Kian, Behnam Esmaeilian, Saeed Kayedi, Mehrdad |
author_sort | Kian, Behnam |
collection | PubMed |
description | Aphallia or penile agenesis is a rare case of the genitourinary system which has an association with upper urinary tract disorder. Failure of fetal genital tubercle formation in the embryonic period is the cause of this disorder. The incidence of aphallia according to previous studies is about 1 in 10-30 million births. We report a case of a child with the absence of the penis with associated kidney hypoplasia and vesicorectal fistula. |
format | Online Article Text |
id | pubmed-9530489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95304892022-10-05 A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula Kian, Behnam Esmaeilian, Saeed Kayedi, Mehrdad Radiol Case Rep Case Report Aphallia or penile agenesis is a rare case of the genitourinary system which has an association with upper urinary tract disorder. Failure of fetal genital tubercle formation in the embryonic period is the cause of this disorder. The incidence of aphallia according to previous studies is about 1 in 10-30 million births. We report a case of a child with the absence of the penis with associated kidney hypoplasia and vesicorectal fistula. Elsevier 2022-09-30 /pmc/articles/PMC9530489/ /pubmed/36204399 http://dx.doi.org/10.1016/j.radcr.2022.08.107 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Kian, Behnam Esmaeilian, Saeed Kayedi, Mehrdad A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula |
title | A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula |
title_full | A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula |
title_fullStr | A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula |
title_full_unstemmed | A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula |
title_short | A rare case report of aphallia with hypoplastic kidney and vesicorectal fistula |
title_sort | rare case report of aphallia with hypoplastic kidney and vesicorectal fistula |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530489/ https://www.ncbi.nlm.nih.gov/pubmed/36204399 http://dx.doi.org/10.1016/j.radcr.2022.08.107 |
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