dc.creatorCOSTA, Helena Olegario da
dc.creatorSOTTO, Mirian N.
dc.creatorVALENTE, Neusa Yuriko Sakai
dc.creatorSILVA, Luiz Fernando Ferraz da
dc.creatorSANCHES JR., Jose Antonio
dc.creatorSILVA, Ana Maria Goncalves da
dc.creatorFESTA NETO, Cyro
dc.date.accessioned2012-10-19T17:22:02Z
dc.date.accessioned2018-07-04T15:06:47Z
dc.date.available2012-10-19T17:22:02Z
dc.date.available2018-07-04T15:06:47Z
dc.date.created2012-10-19T17:22:02Z
dc.date.issued2011
dc.identifierAMERICAN JOURNAL OF DERMATOPATHOLOGY, v.33, n.7, p.669-674, 2011
dc.identifier0193-1091
dc.identifierhttp://producao.usp.br/handle/BDPI/21972
dc.identifier10.1097/DAD.0b013e31820d9bf3
dc.identifierhttp://dx.doi.org/10.1097/DAD.0b013e31820d9bf3
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1618745
dc.description.abstractBackground: The prognostic significance of spontaneous regression in melanoma, especially thin lesions, has been a controversial issue for the past 20 years, although recent studies suggest that extensive and late regression may be related to worse prognosis. Many data suggest that lymphangiogenesis predicts metastatic spread in melanoma. Methods: We have quantified lymphatic microvascular density (LMVD) in thin (<= 1.0 mm) superficial spreading melanomas comparing regressive and nonregressive melanomas, regressive and nonregressive areas from the same tumor, and early and late histological stages of regression in the same tumor. In addition, we tried to correlate lymphangiogenesis and tumor growth phase. We conducted histological examinations and immunohistochemical analyses using monoclonal antibody D2-40 with subsequent quantification by image analysis of 37 melanomas, 16 regressive and 21 nonregressive (controls). Results: We found higher LMVD in the late stage of regression compared with nonregressive area (internal control) of regressive melanomas. Conclusions: Our study suggest that the late stage of spontaneous regression in thin melanomas may be related to worse prognosis as it showed higher LMVD, and evidence shows that this is related with increased risk of metastatic spread. But this supposition must be confirmed by a longer follow-up for detection of lymph node metastases.
dc.languageeng
dc.publisherLIPPINCOTT WILLIAMS & WILKINS
dc.relationAmerican Journal of Dermatopathology
dc.rightsCopyright LIPPINCOTT WILLIAMS & WILKINS
dc.rightsclosedAccess
dc.subjectmelanoma
dc.subjectspontaneous neoplasm regression
dc.subjecthistology
dc.subjectprognosis
dc.subjectlymphangiogenesis
dc.titleMicrovascular Lymphatic Density Analysis in Cutaneous Regressive and Nonregressive Superficial Spreading Melanomas Using the Lymphatic Marker D2-40
dc.typeArtículos de revistas


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