Epidermolysis Bullosa associated with pyloric stenosis: A case report

Authors

  • H Herizchi Ghadim
  • S Aslan Abadi
Abstract:

Epidermolysis bullosa are a group of hereditary skin diseases manifested as blisters on the sites of trauma to the skin. According to the level of blister development, epidermolysis bullosa are divided into the following groups: epidermolysis bullosa simplex, junctional epidermolysis bullosa and dystrophic epidermolysis bullosa. The latter two groups are associated with poorer prognosis and higher mortality and morbidity in comparison with the first group due to the mucosal involvement and associated anomalies in other organs. The presented case was a neonate whom was presented with several blisters and erosions on skin since birth as well as clinical findings suggesting stomach outlet obstruction. It is important to evaluate neonates with epidermolysis bullosa for presence of probable associated anomalies.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Epidermolysis Bullosa with Hypertrophic Pyloric Stenosis in a Newborn.

Epidermolysis bullosa (EB) is an inherited blistering disorder characterized by the fragility of the skin and mucous membranes. Extracutaneous manifestations can be associated. We report a unique concomitant occurrence of EB and hypertrophic pyloric stenosis in a newborn.

full text

Case of Epidermolysis Bullosa with Pyloric Atresia

Epidermolysis bullosa (EB) is a rare hereditary disorder characterized by formation of blisters following minor trauma. It has been traditionally categorized by the level of basement membrane zone separation into EB simplex (EBS), junctional EB (JEB), and dystrophic EB (DEB). Recently, hemidesmosomal EB has been proposed as a fourth category, which includes EB with muscular dystrophy and EB wit...

full text

Epidermolysis Bullosa Puriginosa: Report of a Case

Epidermolysis Bullosa Puriginosa is a genetic mechanobullous disease characterized by pruritus, lichenified or nodular prurigo-like lesions, occasional trauma-induced blistering, excoriations, milia, nail dystrophy and albopapuloid lesions that appear at birth or later. Scarring and prurigo are most prominent on the shins. Herein, we report a case with a history of blisters since childhood foll...

full text

Congenital Hypertrophic Pyloric Stenosis: A Case Report

Background Hypertrophic pyloric stenosis (HPS) is a common surgical condition in infancy, and typically presents at 2-4 weeks of age. Case Presentation A full term male neonate in Zeinabieh hospital, Shiraz, Iran was presented with oral feeding intolerance from birth, bile-stained...

full text

Prenatal diagnosis of junctional epidermolysis bullosa associated with pyloric atresia.

Prenatal diagnosis of junctional epidermolysis bullosa associated with pyloric atresia was carried out in a couple at risk. Their two previous children had died during the first months of life of the same disorder despite surgery for the pyloric abnormality. Ultrastructural study of fetal skin biopsies obtained at 18 weeks' gestation showed dermal-epidermal separation at the lamina lucida level...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 8  issue suppl

pages  45- 48

publication date 2005-10-01

By following a journal you will be notified via email when a new issue of this journal is published.

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023