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J Am Acad Dermatol ; 90(2): 309-318, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-37988042

RESUMO

BACKGROUND: Dermoscopic and reflectance confocal microscopy (RCM) correlations between morphologic groups of melanoma have not yet been described. OBJECTIVE: Describe and compare dermoscopic and RCM features of cutaneous melanomas with histopathological confirmation. METHODS: Single center, retrospective analysis of consecutive melanomas evaluated with RCM (2015-2019). Lesions were clinically classified as typical, nevus-like, amelanotic/nonmelanoma skin cancer (NMSC)-like, seborrheic keratosis (SK)-like and lentigo/lentigo maligna (LM)-like. Presence or absence of common facial and nonfacial melanoma dermoscopic and RCM patterns were recorded. Clusters were compared with typical lesions by multivariate logistic regression. RESULTS: Among 583 melanoma lesions, significant differences between clusters were evident (compared to typical lesions). Observation of dermoscopic features (>50% of lesions) in amelanotic/NMSC-like lesions consistently displayed 3 patterns (atypical network, atypical vascular pattern + regression structures), and nevus-like and SK-like lesions and lentigo/LM-like lesions consistently displayed 2 patterns (atypical network + regression structures, and nonevident follicles + heavy pigmentation intensity). Differences were less evident with RCM, as almost all lesions were consistent with melanoma diagnosis. LIMITATIONS: Small SK-like lesions sample, single RCM analyses (no reproduction of outcome). CONCLUSION: RCM has the potential to augment our ability to consistently and accurately diagnose melanoma independently of clinical and dermoscopic features.


Assuntos
Sarda Melanótica de Hutchinson , Ceratose Seborreica , Lentigo , Melanoma , Nevo Pigmentado , Nevo , Neoplasias Cutâneas , Humanos , Melanoma/patologia , Dermoscopia , Estudos Retrospectivos , Neoplasias Cutâneas/patologia , Sarda Melanótica de Hutchinson/patologia , Ceratose Seborreica/diagnóstico , Nevo/diagnóstico por imagem , Nevo Pigmentado/patologia , Lentigo/diagnóstico , Microscopia Confocal , Diagnóstico Diferencial
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