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J Korean Radiol Soc. 1998 Feb;38(2):297-299. Korean. Case Report. https://doi.org/10.3348/jkrs.1998.38.2.297
Oh KS , Choi ST , Jung GS , Huh JD , Suh KS , Joh YD .
Department of Diagnostic Radiology, Gospel Hospital, Medical College of Kosin University.
Department of General Surgery, Mariawhe Mercy Hospital.
Department of Dermatology, Gospel Hospital, Medical College of Kosin University.
Abstract

Epidermolysis bullosa dystrophica is a rare skin disease characterized by milia, nail dystrophy, andblistering of the skin and mucous membranes in response to minimal trauma. A forty years old man had typical skinlesions on the extremities, and the presence of distal phalangeal wedge deformity with soft tissue webbing wasnoted. multiple segmental strictures and ulceration involved the cervical and distal esophagus. Esophageal balloondilatation was therefore performed and dysphagia was relieved. The authors describe a case involving multipleesophageal strictures and musculoskeletal lesion, with clinically and radiologically documented epidermolysisbullosa dystrophica.

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