DIENCEPHALIC SYNDROME IN A PEDIATRIC PATIENT WITH SUPRASELLAR LESION: CASE REPORT AND REVIEW OF LITERATURE

Authors

  • Johnstone Muthoka Department of Surgery, University of Nairobi
  • Christopher Musau Department of Surgery, University of Nairobi

Abstract

Diencephalic syndrome (DES) is an exceedingly rare condition with fewer than 100 cases reported in literature. It presents as failure to thrive (FTT) in pediatric patients associated with central nervous neoplastic lesions in the suprasellar region. Its characteristic signs and symptoms are related to hypothalamic dysfunction, viz, emaciated body, normal linear growth, normal or precocious intellect, hyperalertness, hyperkinesia and euphoria. Such non-specific presentation usually delays diagnosis of the brain lesion. Herein, we present the case 3-year-old girl with diencephalic syndrome who presented to our neurosurgical unit. She had been earlier managed for Malnutrition and presumed Pulmonary Tuberculosis without much improvement. Further management by the pediatric endocrinologist without change in condition prompted brain imaging. Brain MRI showed a large iso-intense suprasellar lesion, vividly enhancing, causing mild hydrocephalus. Right pterional craniotomy with subtotal resection was done. Histopathology confirmed Hypothalamic Glioma and the patient was referred to Oncology for further management.

Published

26-05-2022

How to Cite

1.
Muthoka J, Musau C. DIENCEPHALIC SYNDROME IN A PEDIATRIC PATIENT WITH SUPRASELLAR LESION: CASE REPORT AND REVIEW OF LITERATURE. EAJNS [Internet]. 2022 May 26 [cited 2024 Feb. 27];1(1). Available from: https://theeajns.org/index.php/eajns/article/view/24

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Section

Conference Abstracts

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