Lhermitte-Duclos Disease is a Component of Cowden Syndrome: Typical MRI Findings

Abstract

Quick Response Code Abstract: Lhermitte-Duclos disease or dysplastic cerebellar gangliocytoma is a rare entity characterized by a hamartomatous lesion in the posterior fossa. Cowden’s syndrome or hamartoma-neoplasia syndrome is a rare underdiagnosed autosomal dominant genodermatosis with high incidence of malignant tumors. Lhermitte-Duclos disease may be a component of Cowden’s syndrome.