Pyloric atresia and epidermolysis bullosa: A fatal association

Author:

Kundu Soham1,Mahapatra Alapan2,Halder Dhrubajyoti3,Halder Pankaj Kumar4

Affiliation:

1. Department of General Surgery, R. G. Kar Medical College, Kolkata, West Bengal, India

2. Department of Pediatric Medicine, R. G. Kar Medical College, Kolkata, West Bengal, India

3. Department of Pediatrics, Dafodil Hospital, Kolkata, West Bengal, India

4. Department of Pediatric Surgery, R. G. Kar Medical College, Kolkata, West Bengal, India

Abstract

Abstract Pyloric atresia (PA) contributes less than 1% of all gastrointestinal atresias with an incidence of 1 in 100,000 newborns. It is often associated with epidermolysis bullosa (EB) or aplasia cutis congenita. This association is believed to be lethal because of the increased risk of developing septicemia, electrolyte imbalance, and protein loss. Here, we attempt to highlight the fatal complications of PA with EB in a 10-day-old female baby and reevaluate the representative features that an astute clinician needs to be aware of.

Publisher

Medknow

Reference8 articles.

1. Congenital pyloric atresia: Clinical features, diagnosis, associated anomalies, management and outcome;Bawazira;Ann Pediatr Surg,2017

2. Missed congenital pyloric atresia with gastric perforation in a neonate;Khan;J Neonat Surg,2012

3. Pyloric atresia associated with epidermolysis bullosa: Report of two cases and review of the literature;Bicakci;Ulus Travma Acil Cerrahi Derg,2012

4. Congenital pyloric atresia and associated anomalies: A case series;Gupta;J Neonatal Surg,2013

5. Pyloric atresia: A report of ten patients;Ksia;Afr J Paediatr Surg,2013

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