Gupta Smriti, Handa Sanjeev, Chatterjee Debajyoti, De Dipankar, Mahajan Rahul
Department of Dermatology, Venereology, and Leprology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Indian Dermatol Online J. 2024 Jul 15;15(5):834-836. doi: 10.4103/idoj.idoj_503_23. eCollection 2024 Sep-Oct.
Epidermolysis bullosa (EB) is a heterogeneous group of genetic disorders characterized by the formation of blisters either spontaneously or at the sites of trauma. These heal with post-inflammatory hypopigmentation, scarring, or milia formation. We hereby present a child who presented with widespread hypopigmented atrophic areas, blistering at trauma-prone sites, and nail dystrophy. The significance of this particular case lies in the challenge of distinguishing between epidermolysis bullosa and bullous extragenital lichen sclerosus et atrophicus.
大疱性表皮松解症（EB）是一组遗传性疾病，其特征是自发或在创伤部位形成水疱。这些水疱愈合后会出现炎症后色素减退、瘢痕形成或粟丘疹。我们在此报告一名儿童，其表现为广泛的色素减退性萎缩区域、易发生创伤部位的水疱形成以及甲营养不良。这个特殊病例的意义在于区分大疱性表皮松解症和大疱性外生殖器硬化萎缩性苔藓的挑战。
