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Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding.

作者信息

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

出版信息

Cesk Patol. 2025;61(2):92-97.

PMID:40763010
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.

摘要

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