Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature

Detalhes bibliográficos
Autor(a) principal: Labrusco, Miguel
Data de Publicação: 2022
Outros Autores: Oliveira, Sara, Teixeira, Ana, Paulos, Lígia, Oom, Paulo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.25754/pjp.2022.23208
Resumo: Rhabdomyosarcoma is one of the most common neoplasms in paediatrics. However, its location in the temporal region is rare. We report a case of a 6 year old male admitted to the Emergency Department with a recurrent history of right otalgia, with progressive clinical worsening despite seriated antibiotics and corticotherapy. Image characterization with both computer tomography and magnetic resonance imaging were suggestive of a space occupying lesion, confirmed with an exploratory tympanomastoidectomy, that revealed an obliterative polypoid lesion. The samples sent for pathology exam were later confirmed to be a rhabdomyosarcoma. The patient underwent combined chemotherapy and radiotherapy, initially with improvement, however, clinical relapse followed with rapid decline to death 9 months after his first symptoms. This case highlights the importance of a strong clinical suspicion in cases presenting with persistence of common symptoms in pediatrics.
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spelling Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting FeatureCase reportsRhabdomyosarcoma is one of the most common neoplasms in paediatrics. However, its location in the temporal region is rare. We report a case of a 6 year old male admitted to the Emergency Department with a recurrent history of right otalgia, with progressive clinical worsening despite seriated antibiotics and corticotherapy. Image characterization with both computer tomography and magnetic resonance imaging were suggestive of a space occupying lesion, confirmed with an exploratory tympanomastoidectomy, that revealed an obliterative polypoid lesion. The samples sent for pathology exam were later confirmed to be a rhabdomyosarcoma. The patient underwent combined chemotherapy and radiotherapy, initially with improvement, however, clinical relapse followed with rapid decline to death 9 months after his first symptoms. This case highlights the importance of a strong clinical suspicion in cases presenting with persistence of common symptoms in pediatrics.Sociedade Portuguesa de Pediatria2022-01-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25754/pjp.2022.23208eng2184-44532184-3333Labrusco, MiguelOliveira, SaraTeixeira, AnaPaulos, LígiaOom, Pauloinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-08-03T02:58:16Zoai:ojs.revistas.rcaap.pt:article/23208Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:25:37.580893Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
title Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
spellingShingle Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
Labrusco, Miguel
Case reports
title_short Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
title_full Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
title_fullStr Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
title_full_unstemmed Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
title_sort Pediatric Rhabdomyosarcoma with Acute Otitis Media as Presenting Feature
author Labrusco, Miguel
author_facet Labrusco, Miguel
Oliveira, Sara
Teixeira, Ana
Paulos, Lígia
Oom, Paulo
author_role author
author2 Oliveira, Sara
Teixeira, Ana
Paulos, Lígia
Oom, Paulo
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Labrusco, Miguel
Oliveira, Sara
Teixeira, Ana
Paulos, Lígia
Oom, Paulo
dc.subject.por.fl_str_mv Case reports
topic Case reports
description Rhabdomyosarcoma is one of the most common neoplasms in paediatrics. However, its location in the temporal region is rare. We report a case of a 6 year old male admitted to the Emergency Department with a recurrent history of right otalgia, with progressive clinical worsening despite seriated antibiotics and corticotherapy. Image characterization with both computer tomography and magnetic resonance imaging were suggestive of a space occupying lesion, confirmed with an exploratory tympanomastoidectomy, that revealed an obliterative polypoid lesion. The samples sent for pathology exam were later confirmed to be a rhabdomyosarcoma. The patient underwent combined chemotherapy and radiotherapy, initially with improvement, however, clinical relapse followed with rapid decline to death 9 months after his first symptoms. This case highlights the importance of a strong clinical suspicion in cases presenting with persistence of common symptoms in pediatrics.
publishDate 2022
dc.date.none.fl_str_mv 2022-01-24
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dc.language.iso.fl_str_mv eng
language eng
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2184-3333
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dc.publisher.none.fl_str_mv Sociedade Portuguesa de Pediatria
publisher.none.fl_str_mv Sociedade Portuguesa de Pediatria
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