Treatment outcomes and Follow-Up results of a sample of females with Frontal fibrosing Alopecia

Document Type : Original Research Papers

Authors

1 M.S.C. of Dermatology and Andrology

2 Professor of Dermatology and Andrology Faculty of Medicine Benha University

3 Assistant Professor of Dermatology, Venereology and Andrology Faculty of Medicine- Benha University

4 Assistant Professor of Clinical and Chemical Pathology Faculty of Medicine Benha University

Abstract

Background: Scarring alopecia may take several forms, one of which is Frontal Fibrosing Alopecia (FFA), a clinical variation of lichen planopilaris (LPP). Scarring alopecia on the hairline is a characteristic of this condition, which mostly affects women after menopause. Purpose: This research set out to conduct a retrospective trial of FFA in Egypt with the intention of evaluating its many components, including its clinical features and treatment results. Methods: Fifty female patients with frontal fibrosing alopecia were included in the research between January 2021 and January 2023 from the dermatology outpatient clinic of Benha University hospital. All individuals who took part in the study provided their written informed permission. A local ethics committee at Benha Faculty of Medicine reviewed the study and gave its approval for it to include human volunteers. Trichoscopic evaluation of frontal fibrosing alopecia and dermatological evaluation of clinical status were also performed on all patients. Outcomes of treatment and durations of six months to a year of follow-up were recorded.Findings: Our research comprised a total of fifty female patients. Onset occurred at an average age of 47±5.7 years. The typical time frame was 1.5±0.5 years. Additionally, characteristic symptoms of concurrent lichen planus were noted in 21 individuals (22.6%), and 28 patients (30.1%) had thyroid problems. Twelve patients (12.9%) had hypertension, while six patients (6.5%) had diabetes. There were less of other goods. Conclusion: FFA signifies a multi-faceted skin condition that necessitates more research because to the lack of a definitive therapy.

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