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Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study

INTRODUCTION: Minimal knowledge exists regarding skin cancers in Black individuals, which may adversely affect patient care. OBJECTIVES: To describe clinical features and risk factors of skin cancers in Black individuals. METHODS: Retrospective study of Black individuals diagnosed with skin cancer b...

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Autores principales: Manci, Rachel N, Dauscher, Megan, Marchetti, Michael A, Usatine, Richard, Rotemberg, Veronica, Dusza, Stephen W, Marghoob, Ashfaq A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116536/
https://www.ncbi.nlm.nih.gov/pubmed/35646436
http://dx.doi.org/10.5826/dpc.1202a75
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author Manci, Rachel N
Dauscher, Megan
Marchetti, Michael A
Usatine, Richard
Rotemberg, Veronica
Dusza, Stephen W
Marghoob, Ashfaq A
author_facet Manci, Rachel N
Dauscher, Megan
Marchetti, Michael A
Usatine, Richard
Rotemberg, Veronica
Dusza, Stephen W
Marghoob, Ashfaq A
author_sort Manci, Rachel N
collection PubMed
description INTRODUCTION: Minimal knowledge exists regarding skin cancers in Black individuals, which may adversely affect patient care. OBJECTIVES: To describe clinical features and risk factors of skin cancers in Black individuals. METHODS: Retrospective study of Black individuals diagnosed with skin cancer between January 2000 and January 2020 at our institution. RESULTS: 38,589 patients were diagnosed with skin cancer, of which 165 were Black individuals. One-hundred-thirteen of these Black individuals were diagnosed with melanoma, 35 with squamous cell carcinoma (SCC), and 17 with basal cell carcinoma (BCC). Most melanomas (80.0%, n = 90) were of the acral subtype; 75% (6 of 8 cases with dermoscopic images) displayed a parallel ridge pattern (PRP). The surrounding uninvolved background skin was visible in 7 cases, all demonstrating a PRP. This disappeared adjacent to most of the melanoma lesions (n = 4, 57.1%). creating a peripheral hypopigmented “halo”. The nonmelanoma skin cancers were pigmented and had similar dermoscopic features as reported in predominantly White populations. Most SCCs (n = 5, 71.4%) had a hypopigmented “halo” and most BCCs (n = 10, 55.6%) had an accentuated reticular network adjacent to the lesions. CONCLUSIONS: Skin cancers are pigmented in Black individuals. In both acral melanomas and SCCs, we noted a peripheral rim of hypopigmentation between the lesions and the surrounding uninvolved background skin, while BCCs had accentuation of the background pigmentation adjacent to the lesions. Most acral melanomas displayed a PRP, which was also seen in surrounding uninvolved background skin.
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spelling pubmed-91165362022-05-27 Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study Manci, Rachel N Dauscher, Megan Marchetti, Michael A Usatine, Richard Rotemberg, Veronica Dusza, Stephen W Marghoob, Ashfaq A Dermatol Pract Concept Original Article INTRODUCTION: Minimal knowledge exists regarding skin cancers in Black individuals, which may adversely affect patient care. OBJECTIVES: To describe clinical features and risk factors of skin cancers in Black individuals. METHODS: Retrospective study of Black individuals diagnosed with skin cancer between January 2000 and January 2020 at our institution. RESULTS: 38,589 patients were diagnosed with skin cancer, of which 165 were Black individuals. One-hundred-thirteen of these Black individuals were diagnosed with melanoma, 35 with squamous cell carcinoma (SCC), and 17 with basal cell carcinoma (BCC). Most melanomas (80.0%, n = 90) were of the acral subtype; 75% (6 of 8 cases with dermoscopic images) displayed a parallel ridge pattern (PRP). The surrounding uninvolved background skin was visible in 7 cases, all demonstrating a PRP. This disappeared adjacent to most of the melanoma lesions (n = 4, 57.1%). creating a peripheral hypopigmented “halo”. The nonmelanoma skin cancers were pigmented and had similar dermoscopic features as reported in predominantly White populations. Most SCCs (n = 5, 71.4%) had a hypopigmented “halo” and most BCCs (n = 10, 55.6%) had an accentuated reticular network adjacent to the lesions. CONCLUSIONS: Skin cancers are pigmented in Black individuals. In both acral melanomas and SCCs, we noted a peripheral rim of hypopigmentation between the lesions and the surrounding uninvolved background skin, while BCCs had accentuation of the background pigmentation adjacent to the lesions. Most acral melanomas displayed a PRP, which was also seen in surrounding uninvolved background skin. Mattioli 1885 2022-04-01 /pmc/articles/PMC9116536/ /pubmed/35646436 http://dx.doi.org/10.5826/dpc.1202a75 Text en ©2022 Manci et al. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (BY-NC-4.0), https://creativecommons.org/licenses/by-nc/4.0/, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Original Article
Manci, Rachel N
Dauscher, Megan
Marchetti, Michael A
Usatine, Richard
Rotemberg, Veronica
Dusza, Stephen W
Marghoob, Ashfaq A
Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study
title Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study
title_full Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study
title_fullStr Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study
title_full_unstemmed Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study
title_short Features of Skin Cancer in Black Individuals: A Single-Institution Retrospective Cohort Study
title_sort features of skin cancer in black individuals: a single-institution retrospective cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116536/
https://www.ncbi.nlm.nih.gov/pubmed/35646436
http://dx.doi.org/10.5826/dpc.1202a75
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