Isolated Congenital Bilateral Choanal Atresia and Nasopharyngeal Atresia- a case report

Authors

  • Suman Das Pediatrics, Senior Resident, Calcutta National Medical College
  • Nirmalya Sarkar Senior Registrar, Apollo Gleangles Hospital
  • Kaushani Chatterjee Senior Resident, Calcutta National Medical College
  • Ayan Paul Junior Resident, Calcutta National Medical College

DOI:

https://doi.org/10.3329/bjms.v13i1.14454

Keywords:

Choanal atresia, oropharyngeal tube, transnasal surgery

Abstract

A term neonate developed respiratory distress, paradoxical cyanosis (relieved by crying) soon after birth. Inability to insert No.5 French infant feeding tube through the nose into the pharynx led to the diagnosis of Bilateral Choanal Atresia , which was confirmed by HRCT Scan of the nose. Insertion of an oropharyngeal tube reduced the respiratory distress. Extensive investigations did not reveal any other congenital anomaly. The baby was treated with Transnasal Surgery.

DOI: http://dx.doi.org/10.3329/bjms.v13i1.14454

Bangladesh Journal of Medical Science Vol. 13 No. 01 January2014: 91-94

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Author Biography

Ayan Paul, Junior Resident, Calcutta National Medical College

Junior Resident

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Published

2013-12-25

How to Cite

Das, S., Sarkar, N., Chatterjee, K., & Paul, A. (2013). Isolated Congenital Bilateral Choanal Atresia and Nasopharyngeal Atresia- a case report. Bangladesh Journal of Medical Science, 13(1), 91–94. https://doi.org/10.3329/bjms.v13i1.14454

Issue

Vol. 13 No. 1 (2014)

Section

Case Reports

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