Journal of Pediatric Neurology 2023; 21(02): 118-121
DOI: 10.1055/s-0042-1751263
Case Report

Basal Ganglia Germinoma in an Adolescent: A Case Report

Shilpa Kulkarni
1   Division of Pediatric Neurosciences, Bai Jerbai Wadia Hospital For Children, Mumbai, India
,
Anish Ainapure
1   Division of Pediatric Neurosciences, Bai Jerbai Wadia Hospital For Children, Mumbai, India
,
Foram Gala
1   Division of Pediatric Neurosciences, Bai Jerbai Wadia Hospital For Children, Mumbai, India
,
Payal Shah
1   Division of Pediatric Neurosciences, Bai Jerbai Wadia Hospital For Children, Mumbai, India
,
Vrushabh Gavali
1   Division of Pediatric Neurosciences, Bai Jerbai Wadia Hospital For Children, Mumbai, India
› Author Affiliations
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Abstract

Germ cell tumors are rare tumors and may pose a diagnostic dilemma. We present a 15-year-old boy with insidious onset right hemiparesis followed by polyuria and polydipsia. Later, he also developed cognitive decline and speech disturbances. Serial magnetic resonance images (MRIs) over a 2-year period showed progressive atrophy of the left caudate nucleus, along with Wallerian degeneration of the left internal capsule and crus of midbrain. Further in the course, imaging revealed an ill-defined signal intensity involving left ganglio-capsulo-thalamic region with increased perfusion which was suggestive of basal ganglia germinoma. Beta human chorionic gonadotropin levels were mildly elevated. This case illustrates an uncommon presentation of a central nervous system germinoma which is often misdiagnosed in the early stages because of its atypical symptomatology and MRI findings.



Publication History

Received: 08 April 2022

Accepted: 23 May 2022

Article published online:
16 August 2022

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