Type B congenital pyloric atresia: a case report

Authors

  • Dikshant Singh Department of Radio-Diagnosis, PGIMS, Rohtak, Haryana, India
  • T. Seetam Kumar Department of Radio-Diagnosis, PGIMS, Rohtak, Haryana, India
  • Jyotsna Sen Department of Radio-Diagnosis, PGIMS, Rohtak, Haryana, India

DOI:

https://doi.org/10.18203/2320-6012.ijrms20202913

Keywords:

Congenital pyloric atresia, Heineke-Mikulicz pyloroplasty, Neonatal intestinal obstruction

Abstract

This is a case of congenital pyloric atresia type B not associated with any other anomaly rare condition, seen as an isolated anomaly with excellent prognosis) of  two days female child presenting with vomiting since birth. X-ray abdomen showed only stomach air bubble, sonography showed distended stomach with echoes and on barium meal no passage of contrast was seen beyond pyloric antrum even after 24 hours. Patient underwent Heineke-Mikulicz pyloroplasty and postoperative recovery was uneventful.

References

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Farmakis SG, Herman TE, Siegel MJ. Congenital pyloric atresia, type B; with junctional epidermolysis bullosa. J Perinatol. 2014 Jul;34(7):572-3.

Nagra S, Cama JK. Pyloric atresia in a healthy newborne Two stage procedure. J Pediatr Surg Case Reports. 2014;2(1):12-4.

Bawazir OA, Al-Salem AH. Congenital pyloric atresia: Clinical features, diagnosis, associated anomalies, management and outcome. Ann Pediatr Surg. 2017;13(4):188-93.

Tomà P, Mengozzi E, Dell'Acqua AP, Mattioli G, Pieroni G, Fabrizzi G. Pyloric atresia: report of two cases (one associated with epidermolysis bullosa and one associated with multiple intestinal atresias) Pediatr Radiol. 2002;32:552-5.

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Published

2020-06-26

How to Cite

Singh, D., Kumar, T. S., & Sen, J. (2020). Type B congenital pyloric atresia: a case report. International Journal of Research in Medical Sciences, 8(7), 2666–2668. https://doi.org/10.18203/2320-6012.ijrms20202913

Issue

Section

Case Reports