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العنوان
Immunohistochemical study of perforin and fas ligand in vitiligo /
الناشر
May Malek Abdelhamid Kohil ,
المؤلف
May Malek Abdelhamid Kohil
هيئة الاعداد
باحث / May Malek Abdelhamid Kohil
مشرف / Akmal Saad Hassan
مشرف / Sara Bahaa El Din Mahmoud
مشرف / Safinaz Salah El Din
تاريخ النشر
2019
عدد الصفحات
99 P. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الأمراض الجلدية
تاريخ الإجازة
1/12/2019
مكان الإجازة
جامعة القاهرة - كلية الطب - Dermatology
الفهرس
Only 14 pages are availabe for public view

from 125

from 125

Abstract

Background: Several studies demonstrated a major pathological role of melanocyte-specific cytotoxic CD8+T cells in the pathogenesis of vitiligo. It has been suggested that apoptosis, rather than necrosis, is the mechanism of melanocyte depletion in vitiligo. Objectives: The aim of this study was to evaluate the expression and distribution of perforin and fraction of apoptosis stimulation ligand (FasL) in the epidermis and dermis of the perilesional and non lesional vitiligo skin in comparison to controls, to assess their possible role in mediating apoptosis in vitiligo. Methods: Twenty patients with active non segmental vitiligo and 20 healthy controls were enrolled in the study. Skin biopsies were taken from perilesional and non lesional skin of patients with vitiligo, as well as covered skin of controls. Immunostaining for perforin and FasL was performed and the quantitative analysis for the expression of perforin and FasL was carried out in the epidermis and dermis of biopsied specimens. Results: Epidermal perforin, dermal perforin, epidermal FasL, dermal FasL were significantly higher in perilesional as well as non lesional skin than controls. There was a statistically significant positive correlation between epidermal and dermal perforin in perilesional skin. There was a statistically significant positive correlation between epidermal and dermal perforin, as well as epidermal and dermal FasL in non lesional skin. There was a statistically significant positive correlation between epidermal and dermal FasL in controls