Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding.

Dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease (LDD), is a rare lesion of the posterior cranial fossa, classified among glioneuronal and neuronal tumors of the CNS, WHO grade 1. It typically has a characteristic radiological appearance on magnetic resonance imaging in the form of "tiger stripes" on T2-weighted images. In adults, LDD is often associated with Cowden syndrome and PTEN gene mutations. Our case report presents a 51-year-old patient with a somewhat atypical finding on magnetic resonance imaging, where histopathological examination surprisingly revealed dysplastic gangliocytoma of the cerebellum with a PTEN gene mutation, subsequently confirmed to be of germline origin. The patient was then examined for other manifestations of Cowden syndrome and is being followed up in a specialized clinic, with cascade genetic testing also conducted in her family.

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PubMed
Published
2025-01-01
Primary Topic
Glioma Diagnosis and Treatment
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article
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article

Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding.

Radim Brabec, Iva Dolinová, Marián Švajdler, Tomáš Jirásek et al.
PubMed
Glioma Diagnosis and Treatment
article

Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding.

Radim Brabec, Iva Dolinová, Marián Švajdler, Tomáš Jirásek, Jana Engelová, Tomáš Klinger, Markéta Hojsáková, Tereza Piskáčková, Renata Michalovská
article en

Abstract

Dysplastic gangliocytoma of the cerebellum, also known as Lhermitte-Duclos disease (LDD), is a rare lesion of the posterior cranial fossa, classified among glioneuronal and neuronal tumors of the CNS, WHO grade 1. It typically has a characteristic radiological appearance on magnetic resonance imaging in the form of "tiger stripes" on T2-weighted images. In adults, LDD is often associated with Cowden syndrome and PTEN gene mutations. Our case report presents a 51-year-old patient with a somewhat atypical finding on magnetic resonance imaging, where histopathological examination surprisingly revealed dysplastic gangliocytoma of the cerebellum with a PTEN gene mutation, subsequently confirmed to be of germline origin. The patient was then examined for other manifestations of Cowden syndrome and is being followed up in a specialized clinic, with cascade genetic testing also conducted in her family.

PubMedVol. 61(2)
Openalex Percentile: Top 73%
Glioma Diagnosis and Treatment
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Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding. — Radim Brabec, Iva Dolinová, et al. · PubMed (2025) | TGRS Research Map | TGRS