Synovial sarcoma: case report

Detalhes bibliográficos
Autor(a) principal: RIBEIRO,Isabella Lima Arrais
Data de Publicação: 2017
Outros Autores: MONTEIRO,Larissa Cavalcanti, MELO,Ana Carolina Rodrigues de, LYRA,Tácio Candeia, FERREIRA FILHO,Julio Cesar Campos, PAZ,Alexandre Rolim da, BONAN,Paulo Rogério Ferreti, VALENÇA,Ana Maria Gondim
Tipo de documento: Artigo
Idioma: eng
Título da fonte: RGO - Revista Gaúcha de Odontologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1981-86372017000300260
Resumo: ABSTRACT Introduction: Synovial sarcomas are rare and aggressive neoplasms located in the head and neck region and usually occurs in young adults. Presentation of case: This report presents a case of synovial sarcoma in a 15-year-old male patient who sought medical treatment for painful symptoms and associated dysphagia. The lesion was nodular, extensive, localized in the parotid region, and extended to the left cervical region. The patient was treated in a referral hospital with a treatment protocol that initially included chemotherapy for six months and surgery to attempt to excise the lesion, but the surgery was ineffective because removal could have damaged important vital structures. The Computed Tomography scan showed a hypodense area with diffuse growth and no involvement of the facial bones and the histopathological analysis revealed pleomorphic and oval spindle cells with rounded epithelial cells that formed nests surrounded by fibrous tissue. The Immunohistochemistry analysis was conclusive for the diagnosis of a high-grade SS in the parotid and left cervical regions. The medical team opted for palliative treatment with cervical radiotherapy. The patient remained hospitalized for four months after the surgery and died after 15 months since the diagnosis for compromise of airway by fast tumor growth. Conclusion: The synovial sarcoma, when diagnosed late may reduce the survival of patients because of the complications that tumor growth can bring to the prognosis and quality of life.
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spelling Synovial sarcoma: case reportInduction chemotherapyNeoplasmsSynovial sarcomaABSTRACT Introduction: Synovial sarcomas are rare and aggressive neoplasms located in the head and neck region and usually occurs in young adults. Presentation of case: This report presents a case of synovial sarcoma in a 15-year-old male patient who sought medical treatment for painful symptoms and associated dysphagia. The lesion was nodular, extensive, localized in the parotid region, and extended to the left cervical region. The patient was treated in a referral hospital with a treatment protocol that initially included chemotherapy for six months and surgery to attempt to excise the lesion, but the surgery was ineffective because removal could have damaged important vital structures. The Computed Tomography scan showed a hypodense area with diffuse growth and no involvement of the facial bones and the histopathological analysis revealed pleomorphic and oval spindle cells with rounded epithelial cells that formed nests surrounded by fibrous tissue. The Immunohistochemistry analysis was conclusive for the diagnosis of a high-grade SS in the parotid and left cervical regions. The medical team opted for palliative treatment with cervical radiotherapy. The patient remained hospitalized for four months after the surgery and died after 15 months since the diagnosis for compromise of airway by fast tumor growth. Conclusion: The synovial sarcoma, when diagnosed late may reduce the survival of patients because of the complications that tumor growth can bring to the prognosis and quality of life.Faculdade São Leopoldo Mandic2017-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1981-86372017000300260RGO - Revista Gaúcha de Odontologia v.65 n.3 2017reponame:RGO - Revista Gaúcha de Odontologia (Online)instname:Faculdade São Leopoldo Mandic (FSLM)instacron:FSLM10.1590/1981-863720170002000123194info:eu-repo/semantics/openAccessRIBEIRO,Isabella Lima ArraisMONTEIRO,Larissa CavalcantiMELO,Ana Carolina Rodrigues deLYRA,Tácio CandeiaFERREIRA FILHO,Julio Cesar CamposPAZ,Alexandre Rolim daBONAN,Paulo Rogério FerretiVALENÇA,Ana Maria Gondimeng2019-08-06T00:00:00Zoai:scielo:S1981-86372017000300260Revistahttp://revodonto.bvsalud.org/scielo.php?script=sci_serial&pid=1981-8637&lng=pt&nrm=isohttps://old.scielo.br/oai/scielo-oai.php||contato@revistargo.com.br1981-86370103-6971opendoar:2019-08-06T00:00RGO - Revista Gaúcha de Odontologia (Online) - Faculdade São Leopoldo Mandic (FSLM)false
dc.title.none.fl_str_mv Synovial sarcoma: case report
title Synovial sarcoma: case report
spellingShingle Synovial sarcoma: case report
RIBEIRO,Isabella Lima Arrais
Induction chemotherapy
Neoplasms
Synovial sarcoma
title_short Synovial sarcoma: case report
title_full Synovial sarcoma: case report
title_fullStr Synovial sarcoma: case report
title_full_unstemmed Synovial sarcoma: case report
title_sort Synovial sarcoma: case report
author RIBEIRO,Isabella Lima Arrais
author_facet RIBEIRO,Isabella Lima Arrais
MONTEIRO,Larissa Cavalcanti
MELO,Ana Carolina Rodrigues de
LYRA,Tácio Candeia
FERREIRA FILHO,Julio Cesar Campos
PAZ,Alexandre Rolim da
BONAN,Paulo Rogério Ferreti
VALENÇA,Ana Maria Gondim
author_role author
author2 MONTEIRO,Larissa Cavalcanti
MELO,Ana Carolina Rodrigues de
LYRA,Tácio Candeia
FERREIRA FILHO,Julio Cesar Campos
PAZ,Alexandre Rolim da
BONAN,Paulo Rogério Ferreti
VALENÇA,Ana Maria Gondim
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv RIBEIRO,Isabella Lima Arrais
MONTEIRO,Larissa Cavalcanti
MELO,Ana Carolina Rodrigues de
LYRA,Tácio Candeia
FERREIRA FILHO,Julio Cesar Campos
PAZ,Alexandre Rolim da
BONAN,Paulo Rogério Ferreti
VALENÇA,Ana Maria Gondim
dc.subject.por.fl_str_mv Induction chemotherapy
Neoplasms
Synovial sarcoma
topic Induction chemotherapy
Neoplasms
Synovial sarcoma
description ABSTRACT Introduction: Synovial sarcomas are rare and aggressive neoplasms located in the head and neck region and usually occurs in young adults. Presentation of case: This report presents a case of synovial sarcoma in a 15-year-old male patient who sought medical treatment for painful symptoms and associated dysphagia. The lesion was nodular, extensive, localized in the parotid region, and extended to the left cervical region. The patient was treated in a referral hospital with a treatment protocol that initially included chemotherapy for six months and surgery to attempt to excise the lesion, but the surgery was ineffective because removal could have damaged important vital structures. The Computed Tomography scan showed a hypodense area with diffuse growth and no involvement of the facial bones and the histopathological analysis revealed pleomorphic and oval spindle cells with rounded epithelial cells that formed nests surrounded by fibrous tissue. The Immunohistochemistry analysis was conclusive for the diagnosis of a high-grade SS in the parotid and left cervical regions. The medical team opted for palliative treatment with cervical radiotherapy. The patient remained hospitalized for four months after the surgery and died after 15 months since the diagnosis for compromise of airway by fast tumor growth. Conclusion: The synovial sarcoma, when diagnosed late may reduce the survival of patients because of the complications that tumor growth can bring to the prognosis and quality of life.
publishDate 2017
dc.date.none.fl_str_mv 2017-09-01
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1981-863720170002000123194
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dc.publisher.none.fl_str_mv Faculdade São Leopoldo Mandic
publisher.none.fl_str_mv Faculdade São Leopoldo Mandic
dc.source.none.fl_str_mv RGO - Revista Gaúcha de Odontologia v.65 n.3 2017
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