1. Diffuse paediatric cerebellar glioma: two identical imaging phenotypes of an extremely rare entity with disparate pathology.
- Author
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McLaughlin A, Lakshmanan R, Dyke J, Warne R, Saha S, Lind C, and Bynevelt M
- Subjects
- Humans, Magnetic Resonance Imaging, Cerebellum diagnostic imaging, Cerebellar Neoplasms diagnostic imaging, Cerebellar Neoplasms genetics, Glioma diagnostic imaging, Glioma genetics, Glioma pathology, Brain Neoplasms pathology, Hamartoma Syndrome, Multiple genetics, Hamartoma Syndrome, Multiple pathology, Hamartoma Syndrome, Multiple surgery
- Abstract
Although the posterior fossa is a common location for paediatric brain tumours [1], diffuse glioma isolated to the cerebellum is an extremely rare imaging entity. Only two cases of isolated diffuse paediatric cerebellar glioma have been reported in the English language to the best of our knowledge [2, 3], and only one of these cases had a similar imaging phenotype to our cases [3]. Although somewhat similar to Lhermitte-Duclos (dysplastic gangliocytoma of the cerebellum), the appearances are distinct from other neoplastic entities of the paediatric posterior fossa. Clinical presentation and neurological examination findings are vital however to help differentiate other diffuse pathologies involving the cerebellum such as rhombencephalitis. Presented here are two diffuse cerebellar gliomas in children under the age of 3 with near identical imaging phenotypes demonstrating differing histological and molecular genetic profiles., (© 2023. Crown.)
- Published
- 2023
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