Sanchez-Anguiano Maria Elena, Schaberg Kurt B, Truong Trinh T
Davis School of Medicine, University of California, Davis, CA.
Department of Pathology, University of California Davis, Davis, CA.
ACG Case Rep J. 2024 Sep 13;11(9):e01508. doi: 10.14309/crj.0000000000001508. eCollection 2024 Sep.
Esophageal epidermoid metaplasia (EEM) is a rare condition that has not been described in Stevens-Johnson syndrome (SJS) and has only been described once in pediatrics. Neither the relationship, treatment, nor surveillance between SJS, esophageal strictures, and EEM has been established. We report the first case of EEM in an 8-year-old girl with esophageal stricture after SJS. Pediatric patients presenting with dysphagia after SJS should be evaluated for esophageal stricture and subsequent EEM development. Owing to EEM's, association with esophageal squamous cell cancer, close follow-up, biopsy surveillance for dysplasia, endoscopic treatment, and TP53 genetic sequencing should be considered.
食管表皮化生(EEM)是一种罕见病症,在史蒂文斯-约翰逊综合征(SJS)中尚未有过描述,仅在儿科中有过一次报道。SJS、食管狭窄和EEM之间的关系、治疗方法及监测手段均未明确。我们报告了首例患SJS后出现食管狭窄的8岁女孩发生EEM的病例。SJS后出现吞咽困难的儿科患者应评估是否存在食管狭窄及后续EEM的发展情况。鉴于EEM与食管鳞状细胞癌有关,应考虑密切随访、对发育异常进行活检监测、内镜治疗以及TP53基因测序。