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Urachal rhabdomyosarcoma: A case report of an extremely rare localisation
Urachus is a tubular structure connecting the allatois to the bladder's apex, in the embryonic development. We report a rare case of a 5-year-old boy, with no past medical history, complaining of secondary enuresis, pollakiuria and urgent incontinence. Physical exam revealed a hypogastric mass....
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/PMC9121247/ https://www.ncbi.nlm.nih.gov/pubmed/35600805 http://dx.doi.org/10.1016/j.eucr.2022.102109 |
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author | Karray, Amina Sahli, Sondos Rahal, Zohra Aziza, Bochra Jouini, Riadh |
author_facet | Karray, Amina Sahli, Sondos Rahal, Zohra Aziza, Bochra Jouini, Riadh |
author_sort | Karray, Amina |
collection | PubMed |
description | Urachus is a tubular structure connecting the allatois to the bladder's apex, in the embryonic development. We report a rare case of a 5-year-old boy, with no past medical history, complaining of secondary enuresis, pollakiuria and urgent incontinence. Physical exam revealed a hypogastric mass. Echo guided percutaneous biopsy followed by a histological analysis showed embryonal RMS. The remainder of the staging ruled out metastasis. The patient received neoadjuvant chemotherapy before proceeding to complete tumor excision. Surgical exploration revealed that the tumor was primitively related to the urachus. Total resection was performed. The one year follow-up was uneventful. |
format | Online Article Text |
id | pubmed-9121247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91212472022-05-21 Urachal rhabdomyosarcoma: A case report of an extremely rare localisation Karray, Amina Sahli, Sondos Rahal, Zohra Aziza, Bochra Jouini, Riadh Urol Case Rep Pediatrics Urachus is a tubular structure connecting the allatois to the bladder's apex, in the embryonic development. We report a rare case of a 5-year-old boy, with no past medical history, complaining of secondary enuresis, pollakiuria and urgent incontinence. Physical exam revealed a hypogastric mass. Echo guided percutaneous biopsy followed by a histological analysis showed embryonal RMS. The remainder of the staging ruled out metastasis. The patient received neoadjuvant chemotherapy before proceeding to complete tumor excision. Surgical exploration revealed that the tumor was primitively related to the urachus. Total resection was performed. The one year follow-up was uneventful. Elsevier 2022-05-10 /pmc/articles/PMC9121247/ /pubmed/35600805 http://dx.doi.org/10.1016/j.eucr.2022.102109 Text en © 2022 The Authors 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 | Pediatrics Karray, Amina Sahli, Sondos Rahal, Zohra Aziza, Bochra Jouini, Riadh Urachal rhabdomyosarcoma: A case report of an extremely rare localisation |
title | Urachal rhabdomyosarcoma: A case report of an extremely rare localisation |
title_full | Urachal rhabdomyosarcoma: A case report of an extremely rare localisation |
title_fullStr | Urachal rhabdomyosarcoma: A case report of an extremely rare localisation |
title_full_unstemmed | Urachal rhabdomyosarcoma: A case report of an extremely rare localisation |
title_short | Urachal rhabdomyosarcoma: A case report of an extremely rare localisation |
title_sort | urachal rhabdomyosarcoma: a case report of an extremely rare localisation |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121247/ https://www.ncbi.nlm.nih.gov/pubmed/35600805 http://dx.doi.org/10.1016/j.eucr.2022.102109 |
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