Weber F, Bauer J W, Sepp N, Högler W, Salmhofer W, Hintner H, Fritsch P
Department of Dermatology and Venereology, University of Innsbruck, Austria.
Acta Derm Venereol. 2001 Jun-Jul;81(3):189-92. doi: 10.1080/000155501750376285.
We report here on three patients suffering from recessive dystrophic epidermolysis bullosa and one suffering from generalized atrophic benign epidermolysis bullosa, all of whom developed cutaneous squamous cell carcinoma. Our observations and a review of the literature suggest that squamous cell carcinoma in generalized atrophic benign epidermolysis bullosa is very infrequent and has a better outcome compared to skin cancer in recessive dystrophic epidermolysis bullosa. These differences could be explained by the distinct pathophysiology and clinical course of each of these variants of epidermolysis bullosa. In contrast to UV-induced skin cancer, the tumours in epidermolysis bullosa develop on distal extremities at sites of chronic wound healing. The cases reported here underline the exceptional importance of early histopathological assessment of suspicious skin lesions in patients with epidermolysis bullosa.
我们在此报告3例隐性营养不良型大疱性表皮松解症患者和1例泛发性萎缩性良性大疱性表皮松解症患者,他们均发生了皮肤鳞状细胞癌。我们的观察结果及文献回顾表明,泛发性萎缩性良性大疱性表皮松解症中的鳞状细胞癌非常罕见,与隐性营养不良型大疱性表皮松解症中的皮肤癌相比,预后更好。这些差异可以通过大疱性表皮松解症每种变体独特的病理生理学和临床病程来解释。与紫外线诱导的皮肤癌不同,大疱性表皮松解症中的肿瘤发生在远端肢体慢性伤口愈合部位。此处报告的病例强调了对大疱性表皮松解症患者可疑皮肤病变进行早期组织病理学评估的特殊重要性。