Vertical growth phase and positive sentinel node in thin melanoma
Autor(a) principal: | |
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Data de Publicação: | 2003 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0100-879X2003000300009 http://repositorio.unifesp.br/handle/11600/1669 |
Resumo: | Sentinel node (SN) status is the most important prognostic factor for localized melanoma. Usually, patients with Breslow thickness of less than 1.0 mm are not included in SN protocols. However, the literature presents a rate ranging from 3 to 7% of nodal recurrence in thin melanoma. Ulceration, regression and high mitotic rate have been considered to be indications for an SN biopsy. The metastatic potential of the vertical growth phase is uncertain. To correlate pathological features in thin melanoma with SN metastasis, we reviewed 358 patients submitted to SN biopsy. Seventy-seven patients with lesions of 1 mm or smaller were included in the study group. Histological evaluation of the primary tumor included thickness, Clark level, mitotic rate, ulceration, regression, and growth phase. Lymphoscintigraphy was performed on all patients. Lymphatic mapping and gamma probe detection were both used for SN biopsy. Histological examination of SN consisted of hematoxylin-eosin and immunohistochemical staining. Median follow-up was 37 months. Six patients had micrometastases. Statistical analysis by the Fisher test showed that ulceration (P = 0.019), high mitotic rate (P = 0.008) and vertical growth phase (P = 0.002) were positively correlated with micrometastases. If other studies confirm these results, more melanoma patients must be submitted to SN biopsy. |
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Vertical growth phase and positive sentinel node in thin melanomaThin melanomaSentinel nodeLymphoscintigraphyImmunohistochemistryMicrometastasisSentinel node (SN) status is the most important prognostic factor for localized melanoma. Usually, patients with Breslow thickness of less than 1.0 mm are not included in SN protocols. However, the literature presents a rate ranging from 3 to 7% of nodal recurrence in thin melanoma. Ulceration, regression and high mitotic rate have been considered to be indications for an SN biopsy. The metastatic potential of the vertical growth phase is uncertain. To correlate pathological features in thin melanoma with SN metastasis, we reviewed 358 patients submitted to SN biopsy. Seventy-seven patients with lesions of 1 mm or smaller were included in the study group. Histological evaluation of the primary tumor included thickness, Clark level, mitotic rate, ulceration, regression, and growth phase. Lymphoscintigraphy was performed on all patients. Lymphatic mapping and gamma probe detection were both used for SN biopsy. Histological examination of SN consisted of hematoxylin-eosin and immunohistochemical staining. Median follow-up was 37 months. Six patients had micrometastases. Statistical analysis by the Fisher test showed that ulceration (P = 0.019), high mitotic rate (P = 0.008) and vertical growth phase (P = 0.002) were positively correlated with micrometastases. If other studies confirm these results, more melanoma patients must be submitted to SN biopsy.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de CirurgiaUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de PatologiaHospital Israelita Albert Einstein Serviço de Medicina NuclearUNIFESP, EPM, Depto. de CirurgiaUNIFESP, EPM, Depto. de PatologiaSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Hospital Israelita Albert Einstein Serviço de Medicina NuclearOliveira Filho, Renato Santos de [UNIFESP]Ferreira, Lydia Masako [UNIFESP]Biasi, Luciano Jose [UNIFESP]Enokihara, Mílvia Maria Simões e Silva [UNIFESP]Paiva, Geruza Rezende [UNIFESP]Wagner, Jairo2015-06-14T13:29:57Z2015-06-14T13:29:57Z2003-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion347-350application/pdfhttp://dx.doi.org/10.1590/S0100-879X2003000300009Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 36, n. 3, p. 347-350, 2003.10.1590/S0100-879X2003000300009S0100-879X2003000300009.pdf0100-879XS0100-879X2003000300009http://repositorio.unifesp.br/handle/11600/1669WOS:000181920300009engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-05T22:48:25Zoai:repositorio.unifesp.br/:11600/1669Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-05T22:48:25Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Vertical growth phase and positive sentinel node in thin melanoma |
title |
Vertical growth phase and positive sentinel node in thin melanoma |
spellingShingle |
Vertical growth phase and positive sentinel node in thin melanoma Oliveira Filho, Renato Santos de [UNIFESP] Thin melanoma Sentinel node Lymphoscintigraphy Immunohistochemistry Micrometastasis |
title_short |
Vertical growth phase and positive sentinel node in thin melanoma |
title_full |
Vertical growth phase and positive sentinel node in thin melanoma |
title_fullStr |
Vertical growth phase and positive sentinel node in thin melanoma |
title_full_unstemmed |
Vertical growth phase and positive sentinel node in thin melanoma |
title_sort |
Vertical growth phase and positive sentinel node in thin melanoma |
author |
Oliveira Filho, Renato Santos de [UNIFESP] |
author_facet |
Oliveira Filho, Renato Santos de [UNIFESP] Ferreira, Lydia Masako [UNIFESP] Biasi, Luciano Jose [UNIFESP] Enokihara, Mílvia Maria Simões e Silva [UNIFESP] Paiva, Geruza Rezende [UNIFESP] Wagner, Jairo |
author_role |
author |
author2 |
Ferreira, Lydia Masako [UNIFESP] Biasi, Luciano Jose [UNIFESP] Enokihara, Mílvia Maria Simões e Silva [UNIFESP] Paiva, Geruza Rezende [UNIFESP] Wagner, Jairo |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Hospital Israelita Albert Einstein Serviço de Medicina Nuclear |
dc.contributor.author.fl_str_mv |
Oliveira Filho, Renato Santos de [UNIFESP] Ferreira, Lydia Masako [UNIFESP] Biasi, Luciano Jose [UNIFESP] Enokihara, Mílvia Maria Simões e Silva [UNIFESP] Paiva, Geruza Rezende [UNIFESP] Wagner, Jairo |
dc.subject.por.fl_str_mv |
Thin melanoma Sentinel node Lymphoscintigraphy Immunohistochemistry Micrometastasis |
topic |
Thin melanoma Sentinel node Lymphoscintigraphy Immunohistochemistry Micrometastasis |
description |
Sentinel node (SN) status is the most important prognostic factor for localized melanoma. Usually, patients with Breslow thickness of less than 1.0 mm are not included in SN protocols. However, the literature presents a rate ranging from 3 to 7% of nodal recurrence in thin melanoma. Ulceration, regression and high mitotic rate have been considered to be indications for an SN biopsy. The metastatic potential of the vertical growth phase is uncertain. To correlate pathological features in thin melanoma with SN metastasis, we reviewed 358 patients submitted to SN biopsy. Seventy-seven patients with lesions of 1 mm or smaller were included in the study group. Histological evaluation of the primary tumor included thickness, Clark level, mitotic rate, ulceration, regression, and growth phase. Lymphoscintigraphy was performed on all patients. Lymphatic mapping and gamma probe detection were both used for SN biopsy. Histological examination of SN consisted of hematoxylin-eosin and immunohistochemical staining. Median follow-up was 37 months. Six patients had micrometastases. Statistical analysis by the Fisher test showed that ulceration (P = 0.019), high mitotic rate (P = 0.008) and vertical growth phase (P = 0.002) were positively correlated with micrometastases. If other studies confirm these results, more melanoma patients must be submitted to SN biopsy. |
publishDate |
2003 |
dc.date.none.fl_str_mv |
2003-03-01 2015-06-14T13:29:57Z 2015-06-14T13:29:57Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0100-879X2003000300009 Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 36, n. 3, p. 347-350, 2003. 10.1590/S0100-879X2003000300009 S0100-879X2003000300009.pdf 0100-879X S0100-879X2003000300009 http://repositorio.unifesp.br/handle/11600/1669 WOS:000181920300009 |
url |
http://dx.doi.org/10.1590/S0100-879X2003000300009 http://repositorio.unifesp.br/handle/11600/1669 |
identifier_str_mv |
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 36, n. 3, p. 347-350, 2003. 10.1590/S0100-879X2003000300009 S0100-879X2003000300009.pdf 0100-879X S0100-879X2003000300009 WOS:000181920300009 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal of Medical and Biological Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
347-350 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268363776458752 |