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2021 ERN-Skin 共识临床立场声明:大疱性表皮松解症的实际管理

2021-09-21 欧洲罕见皮肤病网络European Network for Rare Skin Disorders JEADV

遗传性大疱性表皮松解症 (EB) 包括罕见的疾病,表现为皮肤和粘膜的脆弱和起泡,临床严重程度不同。由于疾病的罕见性和复杂性、广泛的皮肤外表现以及对患者和家庭成员日常生活的深远影响,EB ​​的管理具有

中文标题:

2021 ERN-Skin 共识临床立场声明:大疱性表皮松解症的实际管理

发布日期:

2021-09-21

简要介绍:

遗传性大疱性表皮松解症 (EB) 包括罕见的疾病,表现为皮肤和粘膜的脆弱和起泡,临床严重程度不同。由于疾病的罕见性和复杂性、广泛的皮肤外表现以及对患者和家庭成员日常生活的深远影响,EB ​​的管理具有挑战性。尽管每个欧洲国家都有为 EB 提供多学科护理的参考中心,但通常由不专门研究这种罕见疾病的医疗保健专业人员来治疗 EB 患者。在这里,欧洲罕见和未确诊皮肤病参考网络 (ERN-Skin, https://ern-skin.eu) 为最常见的临床问题、皮肤水疱和伤口、口腔表现、疼痛和瘙痒的诊断和管理提出实用建议。

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Acad Dermatol Venereol - 2021 - Has - Practical management of epidermolysis bullosa consensus clinical position statement.pdf
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