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العنوان
Efficacy and Safety of Diphenylcyclopropenone (DPCP) as a Depigmenting Therapy in Extensive Vitiligo /
المؤلف
Abdelmotaleb, Maysoon Asem Elsayed.
هيئة الاعداد
باحث / ميسون عاصم السيد عبدالمطلب
مشرف / مروى عبد الله
مشرف / رانيا محمود الحسيني
مشرف / رانيا محمود الحسيني
تاريخ النشر
2021.
عدد الصفحات
125p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الأمراض الجلدية
تاريخ الإجازة
1/1/2021
مكان الإجازة
جامعة عين شمس - كلية الطب - الامراض الجلدية
الفهرس
Only 14 pages are availabe for public view

from 125

from 125

Abstract

SUMMARY
P
atients with extensive vitiligo who have residual pigmentation affecting exposed areas especially acral sites or patients with vitiligo universalis often seek depigmentation. At present, there is no ideal depigmenting therapy available. Possible options include; monobenzyl ether of hydroquinone (MBEH) cream, phenol, cryotherapy and Q-switched lasers. Diphenylcyclopropenone (DPCP) has been reported to rarely cause vitiligo as a side effect during the treatment of alopecia areata.
The aim of the present work was to evaluate the efficacy and safety of DPCP as a depigmenting therapy in extensive Vitiligo.
This is a pilot single arm clinical trial. Twenty patients with extensive vitiligo were recruited from the vitiligo outpatient clinic of Dermatology, Venereology and Andrology Department, Ain Shams University Hospitals. We used DPCP applied topically to residual pigmented patches (sensitization session then therapeutic sessions).
Depigmentation occurred among 5 patients (25% of cases). Depigmentation occurred in different tested sites including the scalp, forearm and back within 4 – 8 weeks. Itching and blister formation were the main side effects leading to intolerability and drop-outs to the DPCP treatment.
Cosmetic result of DPCP depigmentation was acceptable with no skin atrophy. Our data favors the use of DPCP as a depigmenting agent for treatment of extensive vitiligo using protocols with less concentrations to improve satisfaction of patients.SUMMARY
P
atients with extensive vitiligo who have residual pigmentation affecting exposed areas especially acral sites or patients with vitiligo universalis often seek depigmentation. At present, there is no ideal depigmenting therapy available. Possible options include; monobenzyl ether of hydroquinone (MBEH) cream, phenol, cryotherapy and Q-switched lasers. Diphenylcyclopropenone (DPCP) has been reported to rarely cause vitiligo as a side effect during the treatment of alopecia areata.
The aim of the present work was to evaluate the efficacy and safety of DPCP as a depigmenting therapy in extensive Vitiligo.
This is a pilot single arm clinical trial. Twenty patients with extensive vitiligo were recruited from the vitiligo outpatient clinic of Dermatology, Venereology and Andrology Department, Ain Shams University Hospitals. We used DPCP applied topically to residual pigmented patches (sensitization session then therapeutic sessions).
Depigmentation occurred among 5 patients (25% of cases). Depigmentation occurred in different tested sites including the scalp, forearm and back within 4 – 8 weeks. Itching and blister formation were the main side effects leading to intolerability and drop-outs to the DPCP treatment.
Cosmetic result of DPCP depigmentation was acceptable with no skin atrophy. Our data favors the use of DPCP as a depigmenting agent for treatment of extensive vitiligo using protocols with less concentrations to improve satisfaction of patients.