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Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature

Pulmonary synovial sarcoma is a rare malignant tumor accounting for 10% of soft tissue sarcomas. It usually arises from the limbs and its occurrence in the lung is exceptional. We here report a clinical case of pulmonary synovial sarcoma in a 54-year-old man detected at a localised stage. This extre...

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Autores principales: Remy, Onana, Messouna, Mohammed, Akimana, Gloria, Kamdem, Marius, Errihani, Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7422737/
https://www.ncbi.nlm.nih.gov/pubmed/32849992
http://dx.doi.org/10.11604/pamj.2020.36.137.23034
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author Remy, Onana
Messouna, Mohammed
Akimana, Gloria
Kamdem, Marius
Errihani, Hassan
author_facet Remy, Onana
Messouna, Mohammed
Akimana, Gloria
Kamdem, Marius
Errihani, Hassan
author_sort Remy, Onana
collection PubMed
description Pulmonary synovial sarcoma is a rare malignant tumor accounting for 10% of soft tissue sarcomas. It usually arises from the limbs and its occurrence in the lung is exceptional. We here report a clinical case of pulmonary synovial sarcoma in a 54-year-old man detected at a localised stage. This extremely rare tumor has a specific immunohistochemical phenotype. This provides strong support for diagnosis. Cytogenetic study confirms the diagnosis by showing the presence of specific translocation t (X; 18). This is highly characteristic of synovial sarcoma regardless of its anatomical location. This study highlights the anatomo-clinical, therapeutic and prognostic characteristics of this rare tumor often unknown to clinicians.
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spelling pubmed-74227372020-08-25 Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature Remy, Onana Messouna, Mohammed Akimana, Gloria Kamdem, Marius Errihani, Hassan Pan Afr Med J Case Report Pulmonary synovial sarcoma is a rare malignant tumor accounting for 10% of soft tissue sarcomas. It usually arises from the limbs and its occurrence in the lung is exceptional. We here report a clinical case of pulmonary synovial sarcoma in a 54-year-old man detected at a localised stage. This extremely rare tumor has a specific immunohistochemical phenotype. This provides strong support for diagnosis. Cytogenetic study confirms the diagnosis by showing the presence of specific translocation t (X; 18). This is highly characteristic of synovial sarcoma regardless of its anatomical location. This study highlights the anatomo-clinical, therapeutic and prognostic characteristics of this rare tumor often unknown to clinicians. The African Field Epidemiology Network 2020-06-29 /pmc/articles/PMC7422737/ /pubmed/32849992 http://dx.doi.org/10.11604/pamj.2020.36.137.23034 Text en Copyright: Onana Remy et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Remy, Onana
Messouna, Mohammed
Akimana, Gloria
Kamdem, Marius
Errihani, Hassan
Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature
title Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature
title_full Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature
title_fullStr Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature
title_full_unstemmed Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature
title_short Le synovialosarcome du poumon: à propos d’un cas et revue de la littérature
title_sort le synovialosarcome du poumon: à propos d’un cas et revue de la littérature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7422737/
https://www.ncbi.nlm.nih.gov/pubmed/32849992
http://dx.doi.org/10.11604/pamj.2020.36.137.23034
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