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Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study

BACKGROUND: Alopecia areata (AA) is an autoimmune condition affecting hair-bearing regions of the body. Few studies worldwide have focused exclusively on beard alopecia areata (BAA). AIMS: To describe the clinical associations, comorbidities, and dermoscopy of BAA. MATERIALS AND METHODS: Forty-six p...

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Autores principales: Bhandary, Delanthimar Joshika, Girisha, Banavasi Shanmukha, Mahadevappa, Basanna Nagargund
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859745/
https://www.ncbi.nlm.nih.gov/pubmed/31807442
http://dx.doi.org/10.4103/idoj.IDOJ_508_18
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author Bhandary, Delanthimar Joshika
Girisha, Banavasi Shanmukha
Mahadevappa, Basanna Nagargund
author_facet Bhandary, Delanthimar Joshika
Girisha, Banavasi Shanmukha
Mahadevappa, Basanna Nagargund
author_sort Bhandary, Delanthimar Joshika
collection PubMed
description BACKGROUND: Alopecia areata (AA) is an autoimmune condition affecting hair-bearing regions of the body. Few studies worldwide have focused exclusively on beard alopecia areata (BAA). AIMS: To describe the clinical associations, comorbidities, and dermoscopy of BAA. MATERIALS AND METHODS: Forty-six patients with BAA were recruited for this hospital-based cross-sectional study. Patients with disease onset of less than 1 month, patches showing extension, and appearance of new patches within the past 1 month were grouped under active disease. Dermoscopy was performed using handheld polarized dermoscope. Chi-square test was applied to know the various associations. P value <0.05 was considered statistically significant. STATA 11.2 was used for analysis of data. RESULTS: The mean age was 31.07 ± 8.72 years. The majority (50%) belonged to 20–29 age group. Twenty-two (48%) patients had active disease. Fourteen (30.43%) patients had extra-beard manifestation of AA. Statistically significant association was noted between active disease and extra-beard manifestation (P = 0.034). Diabetes mellitus and hypertension were noted in one and three patients, respectively. Alcohol abuse was noted in six patients and smoking in five patients. Dermoscopic findings such as black dots, short vellus hair, tapering hair, nonfollicular white dots, regrowing hair, yellow dots, and black dots were similar to findings noted in AA. Uncommon findings such as peripilar sign, i-hair, perifollicular hemorrhage, and tulip hair were observed in BAA. LIMITATIONS: Small sample size, lack of follow-up. CONCLUSION: Trichoscopy of BAA may reveal newer nonfollicular findings, in addition to the follicular findings already described in literature for AA.
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spelling pubmed-68597452019-12-05 Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study Bhandary, Delanthimar Joshika Girisha, Banavasi Shanmukha Mahadevappa, Basanna Nagargund Indian Dermatol Online J Original Article BACKGROUND: Alopecia areata (AA) is an autoimmune condition affecting hair-bearing regions of the body. Few studies worldwide have focused exclusively on beard alopecia areata (BAA). AIMS: To describe the clinical associations, comorbidities, and dermoscopy of BAA. MATERIALS AND METHODS: Forty-six patients with BAA were recruited for this hospital-based cross-sectional study. Patients with disease onset of less than 1 month, patches showing extension, and appearance of new patches within the past 1 month were grouped under active disease. Dermoscopy was performed using handheld polarized dermoscope. Chi-square test was applied to know the various associations. P value <0.05 was considered statistically significant. STATA 11.2 was used for analysis of data. RESULTS: The mean age was 31.07 ± 8.72 years. The majority (50%) belonged to 20–29 age group. Twenty-two (48%) patients had active disease. Fourteen (30.43%) patients had extra-beard manifestation of AA. Statistically significant association was noted between active disease and extra-beard manifestation (P = 0.034). Diabetes mellitus and hypertension were noted in one and three patients, respectively. Alcohol abuse was noted in six patients and smoking in five patients. Dermoscopic findings such as black dots, short vellus hair, tapering hair, nonfollicular white dots, regrowing hair, yellow dots, and black dots were similar to findings noted in AA. Uncommon findings such as peripilar sign, i-hair, perifollicular hemorrhage, and tulip hair were observed in BAA. LIMITATIONS: Small sample size, lack of follow-up. CONCLUSION: Trichoscopy of BAA may reveal newer nonfollicular findings, in addition to the follicular findings already described in literature for AA. Wolters Kluwer - Medknow 2019-11-01 /pmc/articles/PMC6859745/ /pubmed/31807442 http://dx.doi.org/10.4103/idoj.IDOJ_508_18 Text en Copyright: © 2019 Indian Dermatology Online Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Bhandary, Delanthimar Joshika
Girisha, Banavasi Shanmukha
Mahadevappa, Basanna Nagargund
Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study
title Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study
title_full Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study
title_fullStr Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study
title_full_unstemmed Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study
title_short Clinico-Dermoscopic Pattern of Beard Alopecia Areata: A Cross-Sectional Study
title_sort clinico-dermoscopic pattern of beard alopecia areata: a cross-sectional study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6859745/
https://www.ncbi.nlm.nih.gov/pubmed/31807442
http://dx.doi.org/10.4103/idoj.IDOJ_508_18
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