盘状蛋白结构域受体1在瘢痕疙瘩中的免疫组织化学表达

R. Samaka, Amr El Meanawy, Mohammed A. Basha, Shimaa Abdel-Raouf
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摘要

目的探讨盘状蛋白结构域受体1 (DDR1)在瘢痕疙瘩瘢痕中的作用。瘢痕疙瘩是由惰性的胶原蛋白团形成的。因此,胶原蛋白和DDR1的表达可能决定了组织瘢痕的性质和程度。患者和方法本病例对照研究对20例瘢痕疙瘩患者和40例年龄匹配、性别匹配和部位匹配的表面健康志愿者的表面正常皮肤进行了研究。皮肤活检送Menoufia大学医学院病理学系进行组织病理学评估和DDR1免疫组织化学染色。结果DDR1在瘢痕疙瘩(病灶及病灶周围)表皮表达均为阳性。其强度在所有病变活检中均为轻度,在病灶周围活检中仅占20%。真皮表达在所有病变周围病例中呈阳性,只有30%的病变活检呈阳性。DDR1在瘢痕疙瘩表皮和真皮中的表达强度在病变和病变周围瘢痕疙瘩中有显著差异(P < 0.001)。病变瘢痕疙瘩表皮和真皮中DDR1表达h值与病变周围瘢痕疙瘩有显著性差异(P < 0.001)。病变表皮组与病变真皮组瘢痕疙瘩h评分呈显著正相关(r = 0.552;P = 0.012)。在对照组中,所有活组织检查均发现DDR1表皮阳性表达,细胞质定位和基底地形。轻度占52.5%,中度占47.5%。H-score的平均±SD值为81.50±39.52。所有活组织检查均发现DDR1阳性真皮表达,具有细胞质定位和基底地形。50%为轻度,50%为中度。H-score的平均±SD值为82±27.38。结论DDR1在瘢痕疙瘩中的表达可能与瘢痕的早期发病有关。
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Immunohistochemical expression of discoidin domain receptor 1 in keloid scar
Objectives To assess the role of discoidin domain receptor 1 (DDR1) in keloid scar. Background Keloid scars are formed of inert masses of collagen. Therefore, expression of collagen and DDR1 may determine the nature and extent of tissue scarring. Patients and methods This case–control study was carried out on 20 patients presented with keloid and 40 age-matched, sex-matched, and site-matched apparently normal skin from apparently healthy volunteers. Skin biopsies were sent to the Pathology Department of Faculty of Medicine, Menoufia University, for histopathological assessment and immunohistochemical staining of DDR1. Results Epidermal expression of DDR1 was positive in all keloid cases (lesional and perilesional). Its intensity was mild in all lesional biopsies and in only 20% of perilesional ones. Dermal expression was positive in all perilesional cases and in only 30% of lesional biopsies. A significant difference was found between lesional and perilesional keloid regarding DDR1 expression intensity in the epidermis and dermis (P < 0.001). A significant difference was found between lesional and perilesional keloid regarding DDR1 expression H-score in the epidermis and dermis (P < 0.001). A significant positive correlation was found between lesional epidermal and lesional dermal groups regarding keloid H-score (r = 0.552; P = 0.012). In control group, positive epidermal expression of DDR1 was found in all biopsies, with cytoplasmic localization and basal topography. Mild intensity was seen in 52.5% and moderate intensity was seen in 47.5%. The mean ± SD values of H-score were 81.50 ± 39.52. Positive dermal expression of DDR1 was found in all biopsies, with cytoplasmic localization and basal topography. Mild intensity was seen in 50% and moderate intensity was seen in 50%. The mean ± SD values of H-score were 82 ± 27.38. Conclusion DDR1 expression in keloid scar is suspected in early pathogenesis.
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