Non-functioning paraganglioma of the bladder: case report and literature review
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Revista Brasileira de Cancerologia (Online) |
DOI: | 10.32635/2176-9745.RBC.2004v50n3.2028 |
Texto Completo: | https://rbc.inca.gov.br/index.php/revista/article/view/2028 |
Resumo: | Introduction: Paragangliomas are pheochromocytomas with an extra-adrenal location. They can be found between the base of the skull and the bladder. They account for less than 0.06% of all bladder tumors, and were first reported by Zimmermann in 1953, and Rodriguez-Rubio in 1975. Case report: A 17 year old male patient was admitted to Alto Vale Regional Hospital with hematuria and urinary retention. He was examined but nothing positive was found, after which he was discharged for outpatient treatment. After the vesical tumor was diagnosed, the patient was admitted to Hospital for elective surgical treatment of the tumor. After this, pathological analysis revealed a paraganglioma, confirmed by immunohistochemistry. Eleven months after surgery, the patient remains healthy and assymptomatic. Discussion: Paragangliomas usually appear between 11 and 70 years, and are clinically classified as functioning or non-functioning depending on cathecolaminergic production by the tumor. Ten to fifteen percent of bladder paragangliomas are malignant. The diagnosis is confirmed by urinary vanilmandelic acid and urinary metanephryns, ultrassonography, excretory urography, cistoscopy, computerized tomography, magnetic nuclear resonance, and 131-metaiodobenzilguanidine iodine cintilography, with the last one being the most sensitive according to the literature. The treatment is surgical, and the prognosis is uncertain due to small number of cases reported. |
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Revista Brasileira de Cancerologia (Online) |
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Non-functioning paraganglioma of the bladder: case report and literature reviewParaganglioma não-funcionante de bexiga: relato de caso e revisão da literaturaParagangliomaNeoplasias da bexigaFeocromocitomaTumor vesicalParagangliomaBladder neoplasmsPheochromocytomaVesical tumorIntroduction: Paragangliomas are pheochromocytomas with an extra-adrenal location. They can be found between the base of the skull and the bladder. They account for less than 0.06% of all bladder tumors, and were first reported by Zimmermann in 1953, and Rodriguez-Rubio in 1975. Case report: A 17 year old male patient was admitted to Alto Vale Regional Hospital with hematuria and urinary retention. He was examined but nothing positive was found, after which he was discharged for outpatient treatment. After the vesical tumor was diagnosed, the patient was admitted to Hospital for elective surgical treatment of the tumor. After this, pathological analysis revealed a paraganglioma, confirmed by immunohistochemistry. Eleven months after surgery, the patient remains healthy and assymptomatic. Discussion: Paragangliomas usually appear between 11 and 70 years, and are clinically classified as functioning or non-functioning depending on cathecolaminergic production by the tumor. Ten to fifteen percent of bladder paragangliomas are malignant. The diagnosis is confirmed by urinary vanilmandelic acid and urinary metanephryns, ultrassonography, excretory urography, cistoscopy, computerized tomography, magnetic nuclear resonance, and 131-metaiodobenzilguanidine iodine cintilography, with the last one being the most sensitive according to the literature. The treatment is surgical, and the prognosis is uncertain due to small number of cases reported.Introdução: Os paragangliomas são feocromocitomas de localização extra-adrenal, podendo ser encontrados desde a base do crânio até a bexiga. Representam menos de 0,06% de todos os tumores da bexiga, sendo os primeiros casos publicados por Zimmermann em 1953, e por Rodriguez-Rubio em 1975. Relato do caso: Paciente de 17 anos, masculino, deu entrada no Hospital Regional Alto Vale apresentando hematúria e retenção urinária. Foi investigado sem achados positivos, tendo recebido alta hospitalar para investigação ambulatorial do quadro. Diagnosticado o tumor vesical ambulatorialmente, o paciente foi internado para tratamento cirúrgico eletivo do tumor, cujo exame anátomo-patológico revelou a presença de um paraganglioma, confirmado após imunohistoquímica. Onze meses após a cirurgia o paciente permanece hígido e assintomático. Discussão: A idade de apresentação oscila entre os 11 e os 70 anos. Clinicamente são classificados em funcionantes e não-funcionantes de acordo com a presença de produção catecolaminérgica pela neoplasia. Dez a quinze por cento dos paragangliomas de bexiga são malignos. O diagnóstico é confirmado pela dosagem do Ácido Vanilmandélico e Metanefrinas urinárias, Ultrassonografia, Urografia Excretora, Cistoscopia, Tomografia Computadorizada, Ressonância Nuclear Magnética e a Cintilografia com Iodo 131-Metaiodobenzilguanidina, sendo este último apontado como o mais sensível pela literatura. O tratamento é cirúrgico, e o prognóstico ainda é uma incógnita devido ao ainda pequeno número de casos relatados.INCA2004-09-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelato de Casoapplication/pdfhttps://rbc.inca.gov.br/index.php/revista/article/view/202810.32635/2176-9745.RBC.2004v50n3.2028Revista Brasileira de Cancerologia; Vol. 50 No. 3 (2004): July/Aug./Sept; 227-232Revista Brasileira de Cancerologia; Vol. 50 Núm. 3 (2004): jul./ago/sept.; 227-232Revista Brasileira de Cancerologia; v. 50 n. 3 (2004): jul./ago.set.; 227-2322176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporhttps://rbc.inca.gov.br/index.php/revista/article/view/2028/1249Silva, Ulysses Messias da Manteuffel, Ricardo Alexandre Serapião, Mônica Sedrez, Roberto Carlos info:eu-repo/semantics/openAccess2021-11-29T20:32:32Zoai:rbc.inca.gov.br:article/2028Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2021-11-29T20:32:32Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false |
dc.title.none.fl_str_mv |
Non-functioning paraganglioma of the bladder: case report and literature review Paraganglioma não-funcionante de bexiga: relato de caso e revisão da literatura |
title |
Non-functioning paraganglioma of the bladder: case report and literature review |
spellingShingle |
Non-functioning paraganglioma of the bladder: case report and literature review Non-functioning paraganglioma of the bladder: case report and literature review Silva, Ulysses Messias da Paraganglioma Neoplasias da bexiga Feocromocitoma Tumor vesical Paraganglioma Bladder neoplasms Pheochromocytoma Vesical tumor Silva, Ulysses Messias da Paraganglioma Neoplasias da bexiga Feocromocitoma Tumor vesical Paraganglioma Bladder neoplasms Pheochromocytoma Vesical tumor |
title_short |
Non-functioning paraganglioma of the bladder: case report and literature review |
title_full |
Non-functioning paraganglioma of the bladder: case report and literature review |
title_fullStr |
Non-functioning paraganglioma of the bladder: case report and literature review Non-functioning paraganglioma of the bladder: case report and literature review |
title_full_unstemmed |
Non-functioning paraganglioma of the bladder: case report and literature review Non-functioning paraganglioma of the bladder: case report and literature review |
title_sort |
Non-functioning paraganglioma of the bladder: case report and literature review |
author |
Silva, Ulysses Messias da |
author_facet |
Silva, Ulysses Messias da Silva, Ulysses Messias da Manteuffel, Ricardo Alexandre Serapião, Mônica Sedrez, Roberto Carlos Manteuffel, Ricardo Alexandre Serapião, Mônica Sedrez, Roberto Carlos |
author_role |
author |
author2 |
Manteuffel, Ricardo Alexandre Serapião, Mônica Sedrez, Roberto Carlos |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Silva, Ulysses Messias da Manteuffel, Ricardo Alexandre Serapião, Mônica Sedrez, Roberto Carlos |
dc.subject.por.fl_str_mv |
Paraganglioma Neoplasias da bexiga Feocromocitoma Tumor vesical Paraganglioma Bladder neoplasms Pheochromocytoma Vesical tumor |
topic |
Paraganglioma Neoplasias da bexiga Feocromocitoma Tumor vesical Paraganglioma Bladder neoplasms Pheochromocytoma Vesical tumor |
description |
Introduction: Paragangliomas are pheochromocytomas with an extra-adrenal location. They can be found between the base of the skull and the bladder. They account for less than 0.06% of all bladder tumors, and were first reported by Zimmermann in 1953, and Rodriguez-Rubio in 1975. Case report: A 17 year old male patient was admitted to Alto Vale Regional Hospital with hematuria and urinary retention. He was examined but nothing positive was found, after which he was discharged for outpatient treatment. After the vesical tumor was diagnosed, the patient was admitted to Hospital for elective surgical treatment of the tumor. After this, pathological analysis revealed a paraganglioma, confirmed by immunohistochemistry. Eleven months after surgery, the patient remains healthy and assymptomatic. Discussion: Paragangliomas usually appear between 11 and 70 years, and are clinically classified as functioning or non-functioning depending on cathecolaminergic production by the tumor. Ten to fifteen percent of bladder paragangliomas are malignant. The diagnosis is confirmed by urinary vanilmandelic acid and urinary metanephryns, ultrassonography, excretory urography, cistoscopy, computerized tomography, magnetic nuclear resonance, and 131-metaiodobenzilguanidine iodine cintilography, with the last one being the most sensitive according to the literature. The treatment is surgical, and the prognosis is uncertain due to small number of cases reported. |
publishDate |
2004 |
dc.date.none.fl_str_mv |
2004-09-30 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Relato de Caso |
format |
article |
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publishedVersion |
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https://rbc.inca.gov.br/index.php/revista/article/view/2028 10.32635/2176-9745.RBC.2004v50n3.2028 |
url |
https://rbc.inca.gov.br/index.php/revista/article/view/2028 |
identifier_str_mv |
10.32635/2176-9745.RBC.2004v50n3.2028 |
dc.language.iso.fl_str_mv |
por |
language |
por |
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https://rbc.inca.gov.br/index.php/revista/article/view/2028/1249 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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INCA |
publisher.none.fl_str_mv |
INCA |
dc.source.none.fl_str_mv |
Revista Brasileira de Cancerologia; Vol. 50 No. 3 (2004): July/Aug./Sept; 227-232 Revista Brasileira de Cancerologia; Vol. 50 Núm. 3 (2004): jul./ago/sept.; 227-232 Revista Brasileira de Cancerologia; v. 50 n. 3 (2004): jul./ago.set.; 227-232 2176-9745 reponame:Revista Brasileira de Cancerologia (Online) instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) instacron:INCA |
instname_str |
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
instacron_str |
INCA |
institution |
INCA |
reponame_str |
Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) |
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Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
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rbc@inca.gov.br |
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1822181974470557696 |
dc.identifier.doi.none.fl_str_mv |
10.32635/2176-9745.RBC.2004v50n3.2028 |