Journal of Pediatric Neurology 2009; 07(03): 307-310
DOI: 10.3233/JPN-2009-0295
Case Report
Georg Thieme Verlag KG Stuttgart – New York

Neurocysticercosis presenting as central diabetes insipidus in a boy

Seema Rohilla
a   Department of Radiodiagnosis & Imaging, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, University of Health Sciences, Rohtak, Haryana, India
,
Manoj Rawal
b   Department of Pediatrics, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, University of Health Sciences, Rohtak, Haryana, India
,
Rohtas K. Yadav
a   Department of Radiodiagnosis & Imaging, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, University of Health Sciences, Rohtak, Haryana, India
,
Amit Ahuja
a   Department of Radiodiagnosis & Imaging, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, University of Health Sciences, Rohtak, Haryana, India
,
Sanjiv Nanda
b   Department of Pediatrics, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, University of Health Sciences, Rohtak, Haryana, India
,
Dhara B. Dhaulakhandi
c   Department of Biotechnology & Molecular Medicine, Pt. B. D. Sharma Post Graduate Institute of Medical Sciences, University of Health Sciences, Rohtak, Haryana, India
› Author Affiliations

Subject Editor:
Further Information

Publication History

12 May 2008

22 December 2008

Publication Date:
30 July 2015 (online)

Abstract

Neurocysticercosis (NCC) is known to have varied presentations ranging from simple psychosis to stroke and death. While NCC may affect any part of brain or spinal cord, endocrinopathies due to NCC involving hypothalamus and pituitary gland are very rare. A 7-year-old child presented with polyuria and polydipsia for 1 year. After ruling out peripheral diabetes insipidus, a magnetic resonance imaging scan of the brain was done which showed a small cystic lesion in the proximal pituitary stalk. Similar cystic lesions were also seen in other areas of the brain. Cerebrospinal fluid enzyme linked immunosorbent assay for cysticercosis was positive. Such a case of NCC involving pituitary stalk and presenting as central diabetes insipidus is, to the best of our knowledge, the first report of both the location and clinical presentation of NCC in children.