Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis

Detalhes bibliográficos
Autor(a) principal: Cordeiro de Almeida, João
Data de Publicação: 2023
Outros Autores: Fernandes, Diogo, Martins, Dora, Agostinho, Pedro Gil, Gomes, Idílio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.25748/arp.28366
Resumo: A 36-year-old female patient seeks her primary care physician for a 2-year history of right back pain associated with diminished strength in her left arm. The patient is referred to our hospital following the findings of a computed tomography scan which shows a nodular, oval-shaped, soft tissue density mass located in the upper third of the right thoracic wall in intimate relation with the intercostal muscles. Above it, in close proximity with the right pulmonary apex and located in the thoracic inlet, there is another mass with the same tomographic characteristics. Surgical resection is conducted and final pathology results are consistent with multicentric, low grade fusocellular neoplasia. Later genetic testing by Sanger sequencing detects the mutation S45F in the CTNNB1 gene, confirming the diagnosis of multifocal extra-abdominal desmoid fibromatosis.
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spelling Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare DiagnosisFibromatose Extra-Abdominal Multifocal: Um Diagnóstico RaroCasos ClínicosA 36-year-old female patient seeks her primary care physician for a 2-year history of right back pain associated with diminished strength in her left arm. The patient is referred to our hospital following the findings of a computed tomography scan which shows a nodular, oval-shaped, soft tissue density mass located in the upper third of the right thoracic wall in intimate relation with the intercostal muscles. Above it, in close proximity with the right pulmonary apex and located in the thoracic inlet, there is another mass with the same tomographic characteristics. Surgical resection is conducted and final pathology results are consistent with multicentric, low grade fusocellular neoplasia. Later genetic testing by Sanger sequencing detects the mutation S45F in the CTNNB1 gene, confirming the diagnosis of multifocal extra-abdominal desmoid fibromatosis.Paciente do sexo feminino de 36 anos recorre ao seu médico de família por dorsalgia associada a sensação de diminuição de força no braço esquerdo com 2 anos de evolução. É encaminhada para o nosso hospital na sequência de tomografia computadorizada torácica que mostra massa nodular com densidade de tecidos moles no terço superior da parede torácica direita e em íntima relação com os músculos intercostais. Acima desta lesão, na dependência do inlet torácico, encontramos outra massa de características semelhantes. É realizada ressecção cirúrgica e estudo anatomopatológico que é consistente com neoplasia fusocelular de baixo grau, multicêntrica. Estudo genético efectuado posteriormente por sequenciação de Sanger detecta a mutação S45F no gene CTNNB1, confirmando o diagnóstico de fibromatose extra-abdominal multifocal.SPRMN2023-09-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25748/arp.28366eng2183-13512183-1351Cordeiro de Almeida, JoãoFernandes, DiogoMartins, DoraAgostinho, Pedro GilGomes, Idílioinfo: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:RCAAP2023-09-29T03:15:53Zoai:ojs.revistas.rcaap.pt:article/28366Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:31:40.064865Repositório 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 Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
Fibromatose Extra-Abdominal Multifocal: Um Diagnóstico Raro
title Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
spellingShingle Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
Cordeiro de Almeida, João
Casos Clínicos
title_short Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
title_full Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
title_fullStr Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
title_full_unstemmed Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
title_sort Multifocal Extra-Abdominal Desmoid Fibromatosis: A Rare Diagnosis
author Cordeiro de Almeida, João
author_facet Cordeiro de Almeida, João
Fernandes, Diogo
Martins, Dora
Agostinho, Pedro Gil
Gomes, Idílio
author_role author
author2 Fernandes, Diogo
Martins, Dora
Agostinho, Pedro Gil
Gomes, Idílio
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Cordeiro de Almeida, João
Fernandes, Diogo
Martins, Dora
Agostinho, Pedro Gil
Gomes, Idílio
dc.subject.por.fl_str_mv Casos Clínicos
topic Casos Clínicos
description A 36-year-old female patient seeks her primary care physician for a 2-year history of right back pain associated with diminished strength in her left arm. The patient is referred to our hospital following the findings of a computed tomography scan which shows a nodular, oval-shaped, soft tissue density mass located in the upper third of the right thoracic wall in intimate relation with the intercostal muscles. Above it, in close proximity with the right pulmonary apex and located in the thoracic inlet, there is another mass with the same tomographic characteristics. Surgical resection is conducted and final pathology results are consistent with multicentric, low grade fusocellular neoplasia. Later genetic testing by Sanger sequencing detects the mutation S45F in the CTNNB1 gene, confirming the diagnosis of multifocal extra-abdominal desmoid fibromatosis.
publishDate 2023
dc.date.none.fl_str_mv 2023-09-27
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