Gambichler Thilo, Mamali Konstantina, Scheel Christina
Dr. Gambichler and Dr. Scheel are with the Department of Dermatology, Venereology and Allergology at Ruhr-University Bochum in Bochum, Germany.
Dr, Mamali is with Cosmetic Derma Medicine in Athens, Greece.
J Clin Aesthet Dermatol. 2020 Sep;13(9):E53-E58. Epub 2020 Sep 1.
We provide a brief review on mid-dermal elastolysis (MDE) and summarize clinical data of 105 patients with MDE who were reported in the literature since the disease was first described in 1977. In doing so, emphasis is placed on pathomechanisms and therapeutic aspects. MDE is a rare, acquired skin disease histopathologically characterized by selective loss of elastic fibers in the mid-dermis. Lesions are commonly observed on the trunk and proximal extremities. These include well-circumscribed patches of fine wrinkles, perifollicular papular protrusions, and persistent reticular erythema. With respect to pathomechanisms, current data suggest that different cell types (e.g., macrophages, fibroblasts) might chronically overexpress matrix metalloproteinases resulting in an enhanced elastolytic activity. Together with decreased expression of the tissue inhibitors of metalloproteinases, this is thought to result in zonal degradation and loss of elastic tissue in the mid-dermis. However, the exact mechanisms leading to the enhanced elastolytic activity in MDE remain elusive. A multifactorial pathogenesis is likely, including genetic predisposition, chronic inflammation, and (auto)immune processes. Moreover, the capacity for elastic fiber renewal appears to be diminished in patients with MDE, limiting regenerative potential and informing possible treatment strategies, for example, by stimulating elastic fiber synthesis. Although the course of MDE is usually benign and asymptomatic, it can cause severe cosmetic problems. Hence, new therapeutic approaches that block increased elastolytic activity and enhance regeneration of elastic tissue observed in MDE patients are required.
我们对真皮中层弹性纤维溶解症(MDE)进行简要综述,并总结自1977年该病首次被描述以来文献中报道的105例MDE患者的临床数据。在此过程中,重点关注发病机制和治疗方面。MDE是一种罕见的获得性皮肤病,其组织病理学特征为真皮中层弹性纤维选择性缺失。病变常见于躯干和近端肢体。这些病变包括边界清晰的细纹斑块、毛囊周围丘疹样突起和持续性网状红斑。关于发病机制,目前的数据表明不同细胞类型(如巨噬细胞、成纤维细胞)可能长期过度表达基质金属蛋白酶,导致弹性蛋白酶活性增强。再加上金属蛋白酶组织抑制剂表达降低,这被认为会导致真皮中层弹性组织的带状降解和丧失。然而,导致MDE中弹性蛋白酶活性增强的确切机制仍不清楚。发病机制可能是多因素的,包括遗传易感性、慢性炎症和(自身)免疫过程。此外,MDE患者弹性纤维更新能力似乎下降,限制了再生潜力,并为可能的治疗策略提供了思路,例如通过刺激弹性纤维合成。虽然MDE的病程通常是良性且无症状的,但它可能会导致严重的美容问题。因此,需要新的治疗方法来阻断MDE患者中观察到的弹性蛋白酶活性增加并增强弹性组织的再生。