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Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania
BACKGROUND: Papulosquamous skin diseases can be challenging to diagnose, especially in dark skin. Dermoscopy is reported to be helpful, but few data are available on its use in skin type IV or darker. OBJECTIVE: To describe dermoscopic features in plaque-type psoriasis (PP), lichen planus (LP), and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Derm101.com
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368079/ https://www.ncbi.nlm.nih.gov/pubmed/30775148 http://dx.doi.org/10.5826/dpc.0901a11 |
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author | Nwako-Mohamadi, Maitseo K. Masenga, John E. Mavura, David Jahanpour, Ola F. Mbwilo, Eva Blum, Andreas |
author_facet | Nwako-Mohamadi, Maitseo K. Masenga, John E. Mavura, David Jahanpour, Ola F. Mbwilo, Eva Blum, Andreas |
author_sort | Nwako-Mohamadi, Maitseo K. |
collection | PubMed |
description | BACKGROUND: Papulosquamous skin diseases can be challenging to diagnose, especially in dark skin. Dermoscopy is reported to be helpful, but few data are available on its use in skin type IV or darker. OBJECTIVE: To describe dermoscopic features in plaque-type psoriasis (PP), lichen planus (LP), and pityriasis rosea (PR) patients attending the Regional Dermatology Training Centre in Moshi, Northern Tanzania, and to compare findings with published data. METHODS: A descriptive cross-sectional study was conducted at a tertiary hospital from October 2016 to June 2017. Fifty-six patients with PP, 25 with LP, and 9 with PR were enrolled consecutively. Clinical diagnosis was confirmed with histopathology in 74.4%. Dermoscopic vascular and nonvascular features from 225 lesions were analyzed. RESULTS: Of the 90 patients enrolled, 58.9% were male and the median age was 50 (interquartile range 32.8–60.0) years. In PP lesions, red dots were found in 64.2% and white scale in 45.5%. In LP lesions the background was violet in 45.5% and 58.2% revealed Wickham striae. In PR lesions a dull red background was found in 50.0%, white scale in 83.3%, but no vessels were detectable. CONCLUSION: Dermoscopy features in PP, LP, and PR in dark skin are mostly similar to those in light skin. |
format | Online Article Text |
id | pubmed-6368079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Derm101.com |
record_format | MEDLINE/PubMed |
spelling | pubmed-63680792019-02-15 Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania Nwako-Mohamadi, Maitseo K. Masenga, John E. Mavura, David Jahanpour, Ola F. Mbwilo, Eva Blum, Andreas Dermatol Pract Concept Articles BACKGROUND: Papulosquamous skin diseases can be challenging to diagnose, especially in dark skin. Dermoscopy is reported to be helpful, but few data are available on its use in skin type IV or darker. OBJECTIVE: To describe dermoscopic features in plaque-type psoriasis (PP), lichen planus (LP), and pityriasis rosea (PR) patients attending the Regional Dermatology Training Centre in Moshi, Northern Tanzania, and to compare findings with published data. METHODS: A descriptive cross-sectional study was conducted at a tertiary hospital from October 2016 to June 2017. Fifty-six patients with PP, 25 with LP, and 9 with PR were enrolled consecutively. Clinical diagnosis was confirmed with histopathology in 74.4%. Dermoscopic vascular and nonvascular features from 225 lesions were analyzed. RESULTS: Of the 90 patients enrolled, 58.9% were male and the median age was 50 (interquartile range 32.8–60.0) years. In PP lesions, red dots were found in 64.2% and white scale in 45.5%. In LP lesions the background was violet in 45.5% and 58.2% revealed Wickham striae. In PR lesions a dull red background was found in 50.0%, white scale in 83.3%, but no vessels were detectable. CONCLUSION: Dermoscopy features in PP, LP, and PR in dark skin are mostly similar to those in light skin. Derm101.com 2019-01-31 /pmc/articles/PMC6368079/ /pubmed/30775148 http://dx.doi.org/10.5826/dpc.0901a11 Text en ©2019 Nwako-Mohamadi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Articles Nwako-Mohamadi, Maitseo K. Masenga, John E. Mavura, David Jahanpour, Ola F. Mbwilo, Eva Blum, Andreas Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania |
title | Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania |
title_full | Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania |
title_fullStr | Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania |
title_full_unstemmed | Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania |
title_short | Dermoscopic Features of Psoriasis, Lichen Planus, and Pityriasis Rosea in Patients With Skin Type IV and Darker Attending the Regional Dermatology Training Centre in Northern Tanzania |
title_sort | dermoscopic features of psoriasis, lichen planus, and pityriasis rosea in patients with skin type iv and darker attending the regional dermatology training centre in northern tanzania |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6368079/ https://www.ncbi.nlm.nih.gov/pubmed/30775148 http://dx.doi.org/10.5826/dpc.0901a11 |
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