Marathe Kalyani, Lu Jun, Morel Kimberly D
Department of Dermatology, Columbia University College of Physicians and Surgeons, 161 Fort Washington Avenue, 12th Floor, New York, NY, 10032, USA.
Department of Dermatology, University of Connecticut School of Medicine, 21 South Road, Farmington, CT, 06032, USA.
Clin Dermatol. 2015 Nov-Dec;33(6):644-56. doi: 10.1016/j.clindermatol.2015.09.007. Epub 2015 Sep 14.
Bullous diseases may be rare; however, this does not preclude the clinician from being familiar with their manifestations and treatment. After ruling out infection, genetically inherited blistering diseases are more likely to be the cause of blistering or erosions in the neonatal period, whereas immunobullous diseases are more common in adults. Published literature on immunobullous disorders reflects information gleaned from case reports and open-label case series; prospective studies and evidence-based treatments are limited. Although there may be overlapping clinical features, significant clinical differences exist between adults and children. Evidence-based treatment guidelines are limited, and information from the adult literature cannot be readily generalized to the pediatric population. This paper reviews the approach to blistering conditions and the differences among bullous pemphigoid, linear immunoglobulin A disease, dermatitis herpetiformis, pemphigus foliaceus, pemphigus vulgaris, and paraneoplastic pemphigus in adult versus pediatric patients.
大疱性疾病可能较为罕见;然而,这并不妨碍临床医生熟悉其表现及治疗方法。排除感染因素后,遗传性大疱性疾病更有可能是新生儿期水疱或糜烂的病因,而免疫性大疱性疾病在成人中更为常见。已发表的关于免疫性大疱性疾病的文献反映了从病例报告和开放标签病例系列中收集到的信息;前瞻性研究和循证治疗方法有限。尽管成人和儿童可能存在重叠的临床特征,但两者之间也存在显著的临床差异。循证治疗指南有限,且来自成人文献的信息不能轻易推广至儿科人群。本文综述了对水疱性疾病的处理方法,以及成人与儿科患者在大疱性类天疱疮、线状免疫球蛋白A病、疱疹样皮炎、落叶型天疱疮、寻常型天疱疮和副肿瘤性天疱疮方面的差异。