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Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity

BACKGROUND: Female pattern hair loss (FPHL) is a progressive hair loss disorder with unclear triggering and supporting factors. Trichoscopic features of each stage of FPHL have not been specifically elaborated previously. AIMS: To analyze characteristics and investigate associations of clinico-labor...

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Autores principales: Zhang, Xingqi, Caulloo, Sillani, Zhao, Ying, Zhang, Bin, Cai, Zeming, Yang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358934/
https://www.ncbi.nlm.nih.gov/pubmed/22628986
http://dx.doi.org/10.4103/0974-7753.96082
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author Zhang, Xingqi
Caulloo, Sillani
Zhao, Ying
Zhang, Bin
Cai, Zeming
Yang, Jian
author_facet Zhang, Xingqi
Caulloo, Sillani
Zhao, Ying
Zhang, Bin
Cai, Zeming
Yang, Jian
author_sort Zhang, Xingqi
collection PubMed
description BACKGROUND: Female pattern hair loss (FPHL) is a progressive hair loss disorder with unclear triggering and supporting factors. Trichoscopic features of each stage of FPHL have not been specifically elaborated previously. AIMS: To analyze characteristics and investigate associations of clinico-laboratory and trichoscopic features of female patients in regard to the severity of hair loss in FPHL and to facilitate its diagnosis using noninvasive scalp dermoscopy (trichoscopy) in Fitzpatrick skin type III patients. MATERIALS AND METHODS: Clinico-laboratory and trichoscopic data from 60 patients with FPHL were analyzed using Spearman's correlation test. RESULTS: Patients had mean age of 34.4±10.6 years and mean duration of hair loss of 4.49±3.76 years. Of all, 45% (27/60) had a family history of pattern hair loss (PHL) and had an earlier onset of hair loss. Stage of hair loss positively correlated with duration and age at presentation. No association was found between the severity of FPHL and laboratory values including anemic and gonadal hormone profiles. Characteristic trichoscopic features (at 10-fold magnification) of FPHL were peripilar signs (PPS) (brown, BPPS and white, WPPS), white dots, scalp pigmentation, and focal atrichia. WPPS, scalp pigmentation, and focal atrichia positively correlated with the stage and duration of hair loss. CONCLUSIONS: Family history of PHL causes an earlier onset of hair loss but does not influence its course or severity. The latter is also not affected by abnormal anemic profile or hormonal levels. PPS, scalp pigmentation, focal atrichia, and white dots are characteristic of PHL. WPPS, scalp pigmentation, and focal atrichia reflect advanced PHL.
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spelling pubmed-33589342012-05-24 Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity Zhang, Xingqi Caulloo, Sillani Zhao, Ying Zhang, Bin Cai, Zeming Yang, Jian Int J Trichology Original Article BACKGROUND: Female pattern hair loss (FPHL) is a progressive hair loss disorder with unclear triggering and supporting factors. Trichoscopic features of each stage of FPHL have not been specifically elaborated previously. AIMS: To analyze characteristics and investigate associations of clinico-laboratory and trichoscopic features of female patients in regard to the severity of hair loss in FPHL and to facilitate its diagnosis using noninvasive scalp dermoscopy (trichoscopy) in Fitzpatrick skin type III patients. MATERIALS AND METHODS: Clinico-laboratory and trichoscopic data from 60 patients with FPHL were analyzed using Spearman's correlation test. RESULTS: Patients had mean age of 34.4±10.6 years and mean duration of hair loss of 4.49±3.76 years. Of all, 45% (27/60) had a family history of pattern hair loss (PHL) and had an earlier onset of hair loss. Stage of hair loss positively correlated with duration and age at presentation. No association was found between the severity of FPHL and laboratory values including anemic and gonadal hormone profiles. Characteristic trichoscopic features (at 10-fold magnification) of FPHL were peripilar signs (PPS) (brown, BPPS and white, WPPS), white dots, scalp pigmentation, and focal atrichia. WPPS, scalp pigmentation, and focal atrichia positively correlated with the stage and duration of hair loss. CONCLUSIONS: Family history of PHL causes an earlier onset of hair loss but does not influence its course or severity. The latter is also not affected by abnormal anemic profile or hormonal levels. PPS, scalp pigmentation, focal atrichia, and white dots are characteristic of PHL. WPPS, scalp pigmentation, and focal atrichia reflect advanced PHL. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3358934/ /pubmed/22628986 http://dx.doi.org/10.4103/0974-7753.96082 Text en Copyright: © International Journal of Trichology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Zhang, Xingqi
Caulloo, Sillani
Zhao, Ying
Zhang, Bin
Cai, Zeming
Yang, Jian
Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity
title Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity
title_full Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity
title_fullStr Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity
title_full_unstemmed Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity
title_short Female Pattern Hair Loss: Clinico-Laboratory Findings and Trichoscopy Depending on Disease Severity
title_sort female pattern hair loss: clinico-laboratory findings and trichoscopy depending on disease severity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358934/
https://www.ncbi.nlm.nih.gov/pubmed/22628986
http://dx.doi.org/10.4103/0974-7753.96082
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