St John's Institute of Dermatology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
Dermatology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Orphanet J Rare Dis. 2020 Jun 6;15(1):142. doi: 10.1186/s13023-020-01403-x.
Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement and complications. A number of emergency situations may occur in the context of EB including obstruction to oral intake from oral or esophageal blisters or scarring, acute airway obstruction, acute urinary retention, sepsis and corneal erosions. Whilst general management principles apply in each of these settings, specific considerations are essential in managing EB to avoid undue trauma or damage to delicate tissues. These recommendations have been developed from a literature review and consensus from experts of the European Network for Rare Skin Disorders (ERN-Skin) to aid decision-making and optimize clinical care by non-EB expert health professionals encountering emergency situations in babies, children and adults with EB.
大疱性表皮松解症(EB)是一组具有皮肤和黏膜表面脆弱特征的遗传疾病。不同类型的 EB 的严重程度差异很大,也会发生皮肤外的累及和并发症。在 EB 背景下可能会出现许多紧急情况,包括口腔或食管水疱或瘢痕引起的口腔摄入受阻、急性气道阻塞、急性尿潴留、败血症和角膜糜烂。虽然这些情况下都适用一般的管理原则,但在管理 EB 时需要特别考虑,以避免对脆弱组织造成不必要的创伤或损害。这些建议是从文献回顾和欧洲罕见皮肤疾病网络(ERN-Skin)专家的共识中制定的,旨在帮助非 EB 专家的医疗保健专业人员在遇到患有 EB 的婴儿、儿童和成人的紧急情况时做出决策并优化临床护理。