Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Rev Gastroenterol Mex ; 76(3): 279-85, 2011.
Article in Spanish | MEDLINE | ID: mdl-22041322

ABSTRACT

Epidermolysis bullosa acquisita (EBA) is a rare auto-immune dermatologic disease, produced by auto-antibodies against colagen VII. We report a 44 years old male patient with EBA diagnosed 15 years before, who presented with progressive disphagia, being diagnosed an esophageal involvement of EBA. The patient was submitted to endoscopic treatment with thermoplastic bougie dilation and intralesional corticosteroid injection. The patient improved clinically with recovery of nutritional status. Esophageal involvement in EBA is very rare and its reason is still unknown. Endoscopic approach must be cautiously performed with the use of small diameter endoscopes, small caliber dilators, intralesional injection of corticosteroid and enteral tube in order to minimize the risks of complications, as well as esophageal rest from food trauma and better reparatory molding of the epithelium.


Subject(s)
Epidermolysis Bullosa Acquisita/complications , Esophageal Stenosis/etiology , Esophageal Stenosis/therapy , Esophagoscopy , Glucocorticoids/administration & dosage , Prednisone/administration & dosage , Adult , Combined Modality Therapy , Dilatation/instrumentation , Humans , Injections, Intralesional , Male
SELECTION OF CITATIONS
SEARCH DETAIL
...