Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa

Epidermolysis bullosa is a genetically transmitted skin disorder that typically manifests with trauma-induced skin blistering, scarring and in some cases mucosal involvement. Esophageal webs, strictures or stenosis can be found in about a third of the patients with the recessive dystrophic ty...

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Main Authors: Zlatko Djurić, Aleksandar Nagorni, Dragoljub Zivanović
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2012-06-01
Series:The Turkish Journal of Pediatrics
Online Access:https://turkjpediatr.org/article/view/1639
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author Zlatko Djurić
Aleksandar Nagorni
Dragoljub Zivanović
author_facet Zlatko Djurić
Aleksandar Nagorni
Dragoljub Zivanović
author_sort Zlatko Djurić
collection DOAJ
description Epidermolysis bullosa is a genetically transmitted skin disorder that typically manifests with trauma-induced skin blistering, scarring and in some cases mucosal involvement. Esophageal webs, strictures or stenosis can be found in about a third of the patients with the recessive dystrophic type of this disease. We report a six-year-old girl with recessive dystrophic epidermolysis bullosa and progressive dysphagia. Almost complete esophageal occlusion was found on barium swallow and esophagoscopy (endoscopic signs of esophagitis were also seen). She was treated successfully with fluoroscopically guided balloon dilatation and esomeprazole. Fluoroscopically guided balloon dilatation and postdilatation use of esomeprazole is a safe and effective therapy for recessive dystrophic epidermolysis bullosa patients with almost complete esophageal occlusion and esophagitis.
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language English
publishDate 2012-06-01
publisher Hacettepe University Institute of Child Health
record_format Article
series The Turkish Journal of Pediatrics
spelling doaj-art-fd4c63e2e1ba4b1e96ecb070e93d4e802025-08-20T03:00:54ZengHacettepe University Institute of Child HealthThe Turkish Journal of Pediatrics0041-43012791-64212012-06-01543Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosaZlatko Djurić0Aleksandar NagorniDragoljub ZivanovićDivision of Gastroenterology, Children's Hospital, Niş, Serbia. Epidermolysis bullosa is a genetically transmitted skin disorder that typically manifests with trauma-induced skin blistering, scarring and in some cases mucosal involvement. Esophageal webs, strictures or stenosis can be found in about a third of the patients with the recessive dystrophic type of this disease. We report a six-year-old girl with recessive dystrophic epidermolysis bullosa and progressive dysphagia. Almost complete esophageal occlusion was found on barium swallow and esophagoscopy (endoscopic signs of esophagitis were also seen). She was treated successfully with fluoroscopically guided balloon dilatation and esomeprazole. Fluoroscopically guided balloon dilatation and postdilatation use of esomeprazole is a safe and effective therapy for recessive dystrophic epidermolysis bullosa patients with almost complete esophageal occlusion and esophagitis. https://turkjpediatr.org/article/view/1639
spellingShingle Zlatko Djurić
Aleksandar Nagorni
Dragoljub Zivanović
Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa
The Turkish Journal of Pediatrics
title Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa
title_full Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa
title_fullStr Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa
title_full_unstemmed Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa
title_short Esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa
title_sort esophagitis and almost complete esophageal occlusion in a girl with epidermolysis bullosa
url https://turkjpediatr.org/article/view/1639
work_keys_str_mv AT zlatkodjuric esophagitisandalmostcompleteesophagealocclusioninagirlwithepidermolysisbullosa
AT aleksandarnagorni esophagitisandalmostcompleteesophagealocclusioninagirlwithepidermolysisbullosa
AT dragoljubzivanovic esophagitisandalmostcompleteesophagealocclusioninagirlwithepidermolysisbullosa