Mauro M A, Parker L A, Hartley W S, Renner J B, Mauro P M
Department of Radiology, University of North Carolina School of Medicine, Chapel Hill 27514.
AJR Am J Roentgenol. 1987 Nov;149(5):925-7. doi: 10.2214/ajr.149.5.925.
Epidermolysis bullosa is a group of dermatologic disorders with varied inheritance patterns having the common manifestation of blister or bulla formation after minor trauma. Sixteen patients with the disease had the following radiographic manifestations: esophageal stricture (16), fecal impaction (six), vaginal stenosis (one), epithelial bridging and fusion of the digits (six), and aspiration changes in the lungs (two). Esophageal strictures involved the pharynx or cervical esophagus in eight cases and were multiple in five; they ranged in length from 2 mm to 15 cm and tended to progress over time. The findings of esophageal stricture, particularly when multiple and involving the proximal esophagus, and/or the presence of distal phalangeal atrophy with soft-tissue webbing suggest the diagnosis of epidermolysis bullosa.
大疱性表皮松解症是一组具有多种遗传模式的皮肤病,其共同表现为轻微创伤后形成水疱或大疱。16例患有该疾病的患者有以下影像学表现:食管狭窄(16例)、粪块嵌塞(6例)、阴道狭窄(1例)、手指上皮桥接和融合(6例)以及肺部吸入性改变(2例)。食管狭窄累及咽部或颈段食管8例,其中5例为多发;长度从2毫米到15厘米不等,且往往随时间进展。食管狭窄的表现,尤其是多发且累及食管近端时,和/或伴有软组织蹼的远节指骨萎缩提示大疱性表皮松解症的诊断。