Abstract
Objective: To evaluate the quality of life and the impact of melasma on women with the disease. Methods: This is a qualitative-quantitative study in which 52 women over 18 years of age with melasma participated. The reflection of melasma in the social, emotional and professional sphere was evaluated by means of a virtual questionnaire, composed of: MELASQoL, DLQI-BRA, HADS Scale and Socio-Economic-Demographic Questionnaire. Students' t-test was applied to the results obtained to compare differences between the scores of the sample. This research was approved by the Ethics and Research with Human Beings Committee. Results: The research evidenced that: 67,3% of the participants did not perform dermatological medical follow-up; 78.8% used makeup to cover their macules; 82,6% and 86,5% felt depressed and less attractive to others; for 48,1% and 71,1% of them, melasma did not affect the performance of daily and leisure activities, as well as work and studies; 36,5% of them did not feel pleasure in leisure moments; and 30,8% did not enjoy the same things as before. Conclusion: We conclude that melasma affects the quality of life of women with this disease. Moreover, dissatisfaction with self-image, combined with daily stress, can worsen anxiety and depression.
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