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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....

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Detalles Bibliográficos
Autores principales: Karray, Amina, Sahli, Sondos, Rahal, Zohra, Aziza, Bochra, Jouini, Riadh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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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