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Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study

BACKGROUND: Progressive macular hypomelanosis (PMH) is a disease of unclear etiology. Propionbacterium acnes (P. acnes) was claimed to be an etiological factor. OBJECTIVES: The purpose of this study was to document the clinicopathological features of PMH in Egyptian patients and to evaluate the ther...

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Autores principales: Selim, Mohamed Khaled, Ahmed, El-Shahat Farag, Abdelgawad, Mamdouh Morsy, El-Kamel, Mohammed Fawzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Derm101.com 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881075/
https://www.ncbi.nlm.nih.gov/pubmed/24396712
http://dx.doi.org/10.5826/dpc.0101a03
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author Selim, Mohamed Khaled
Ahmed, El-Shahat Farag
Abdelgawad, Mamdouh Morsy
El-Kamel, Mohammed Fawzy
author_facet Selim, Mohamed Khaled
Ahmed, El-Shahat Farag
Abdelgawad, Mamdouh Morsy
El-Kamel, Mohammed Fawzy
author_sort Selim, Mohamed Khaled
collection PubMed
description BACKGROUND: Progressive macular hypomelanosis (PMH) is a disease of unclear etiology. Propionbacterium acnes (P. acnes) was claimed to be an etiological factor. OBJECTIVES: The purpose of this study was to document the clinicopathological features of PMH in Egyptian patients and to evaluate the therapeutic outcome. METHODS: Patients with clinical features of PMH were recruited. Wood’s lamp examination, skin scrapings for fungi, and skin biopsy specimens were obtained. Biopsies were stained with hematoxylin and eosin, PAS, Fontana-Masson, and S100 protein. Patients received either narrow-band UVB (nbUVB) or nbUVB plus daily topical clindamycin 1% and benzoyl peroxide gel 5% (bcUVB). The period of active treatment was 14 weeks followed by a follow-up period of 24 weeks. RESULTS: Twenty-nine patients were included. Microscopic evaluation of skin biopsy specimens showed no significant differences between lesional and normal skin. Fontana-Masson stained sections showed overall reduction of melanin granules in the basal layer of lesional skin only and S100 staining did not detect significant differences in the number of melanocytes in lesional and normal skin. Nearly complete repigmentation was reported in 10 patients treated with bcUVB compared to 9 patients treated with nbUVb with no significant differences between both groups after 14 weeks. Only 2 patients in each group retained the pigmentation and the remaining patients returned to the baseline color before treatment. CONCLUSIONS: This study documented the clinicopathological features of PMH among Egyptians. No permanently effective treatment is available. Further studies are needed to prove or disprove the pathogenic role of P. acnes in PMH.
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spelling pubmed-38810752014-01-06 Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study Selim, Mohamed Khaled Ahmed, El-Shahat Farag Abdelgawad, Mamdouh Morsy El-Kamel, Mohammed Fawzy Dermatol Pract Concept Research BACKGROUND: Progressive macular hypomelanosis (PMH) is a disease of unclear etiology. Propionbacterium acnes (P. acnes) was claimed to be an etiological factor. OBJECTIVES: The purpose of this study was to document the clinicopathological features of PMH in Egyptian patients and to evaluate the therapeutic outcome. METHODS: Patients with clinical features of PMH were recruited. Wood’s lamp examination, skin scrapings for fungi, and skin biopsy specimens were obtained. Biopsies were stained with hematoxylin and eosin, PAS, Fontana-Masson, and S100 protein. Patients received either narrow-band UVB (nbUVB) or nbUVB plus daily topical clindamycin 1% and benzoyl peroxide gel 5% (bcUVB). The period of active treatment was 14 weeks followed by a follow-up period of 24 weeks. RESULTS: Twenty-nine patients were included. Microscopic evaluation of skin biopsy specimens showed no significant differences between lesional and normal skin. Fontana-Masson stained sections showed overall reduction of melanin granules in the basal layer of lesional skin only and S100 staining did not detect significant differences in the number of melanocytes in lesional and normal skin. Nearly complete repigmentation was reported in 10 patients treated with bcUVB compared to 9 patients treated with nbUVb with no significant differences between both groups after 14 weeks. Only 2 patients in each group retained the pigmentation and the remaining patients returned to the baseline color before treatment. CONCLUSIONS: This study documented the clinicopathological features of PMH among Egyptians. No permanently effective treatment is available. Further studies are needed to prove or disprove the pathogenic role of P. acnes in PMH. Derm101.com 2011-01-31 /pmc/articles/PMC3881075/ /pubmed/24396712 http://dx.doi.org/10.5826/dpc.0101a03 Text en Copyright ©2011 Selim 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 Research
Selim, Mohamed Khaled
Ahmed, El-Shahat Farag
Abdelgawad, Mamdouh Morsy
El-Kamel, Mohammed Fawzy
Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study
title Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study
title_full Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study
title_fullStr Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study
title_full_unstemmed Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study
title_short Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study
title_sort progressive macular hypomelanosis among egyptian patients: a clinicopathological study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881075/
https://www.ncbi.nlm.nih.gov/pubmed/24396712
http://dx.doi.org/10.5826/dpc.0101a03
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