A Rare Case Report on Frontal Encephalocele

Authors

  • Dinesh Kumar Barolia Department of Pediatric Surgery, J. K. Lon Hospital, S. M. S. Medical College, Jaipur, Rajasthan, India.
  • Sunil Mehra Department of Pediatric Surgery, J. K. Lon Hospital, S. M. S. Medical College, Jaipur, Rajasthan, India.
  • Vinita Chaturvedi Department of Pediatric Surgery, J. K. Lon Hospital, S. M. S. Medical College, Jaipur, Rajasthan, India.
  • Neeraj Tuteja Department of Pediatric Surgery, J. K. Lon Hospital, S. M. S. Medical College, Jaipur, Rajasthan, India.
  • Soumyodhriti Ghosh Department of Pediatric Surgery, J. K. Lon Hospital, S. M. S. Medical College, Jaipur, Rajasthan, India.
  • Ramjee Prasad Department of Pediatric Surgery, J. K. Lon Hospital, S. M. S. Medical College, Jaipur, Rajasthan, India.

DOI:

https://doi.org/10.9734/bpi/rdmmr/v4/4914F

Keywords:

Encephalocele, frontal, frontal encephalocele, frontonasal encephalocele, meninges

Abstract

Background: Frontal encephalocele is less common than occipital encephalocele. Frontal encephalocele is protrusion of brain content through defect in frontal bone. Meninges and part of frontal lobe was protruding through defect in this case. Its management is typical and different approach for repair. We introduce ventriculo peritoneal shunt first to reduce the size of swelling and manage the hydrocephalus.

Case Report: Encephalocele is a congenital anomaly that causes the brain component to protrude through the cranial defect.  We are reporting a case of frontal encephalocele in three month old male child. The swelling was skin covered.

Conclusion: Frontal encephalocele is a rare entity. A case of congenital frontal encephalocele, an uncommon neural tube defect, is described.

Published

2021-10-04

How to Cite

Dinesh Kumar Barolia, Sunil Mehra, Vinita Chaturvedi, Neeraj Tuteja, Soumyodhriti Ghosh, & Ramjee Prasad. (2021). A Rare Case Report on Frontal Encephalocele. Recent Developments in Medicine and Medical Research Vol. 4, 96–100. https://doi.org/10.9734/bpi/rdmmr/v4/4914F