A Case Report of Lhermitte-Duclos Disease in a 10-Month-Old Child Presenting with Hydrocephalus
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چکیده
منابع مشابه
Lhermitte-duclos Disease in a Young Adult Case Report
Dysplastic gangliocytoma of the cerebellum is a very rare lesion. The other names assigned to this pathology are Lhermitte-Duclos disease. ganglioneuroma. hamartoma of the cerebellum. purkengioma. granule cell hypertrophy or granulomolecular hypertrophy of the cerebellum. Only few cases have been reported in the literature (1-20).since the first report by Lhermitte and Duclos (11).Clinically. t...
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متن کاملLhermitte-Duclos disease presenting with positron emission tomography-magnetic resonance fusion imaging: a case report
INTRODUCTION Lhermitte-Duclos disease or dysplastic gangliocytoma of the cerebellum is an extremely rare tumor. It is a slowly enlarging mass within the cerebellar cortex. The majority of cases are diagnosed in the third or fourth decade of life. CASE PRESENTATION We report the case of a 37-year-old Caucasian woman who underwent positron emission tomography-computed tomography with fluorine-1...
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Since 1920, when Lhermitte and Duclos first described a tumorlike abnormality of the cerebellum, which has come to bear their name, there has been an increasing number of reports of this rare entity [1-10]. Most cases have not had radiographic correlation , but there are several reported cases in which CT was part of the pretreatment evaluation [2-7], and one case was demonstrated on low-field ...
متن کاملCowden disease with Lhermitte-Duclos disease: case report.
BACKGROUND We report a case and review the recent literature describing 36 patients with both Lhermitte-Duclos disease (LDD) and Cowden disease (CD). Lhermitte-Duclos disease, or dysplastic gangliocytoma, is a benign hamartomatous condition involving the cerebellum. The presenting symptoms are usually headaches, gait ataxia, and symptoms of lower cranial nerve involvement. Cowden disease is a r...
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ژورنال
عنوان ژورنال: Nepal Journal of Neuroscience
سال: 2019
ISSN: 1813-1956,1813-1948
DOI: 10.3126/njn.v16i3.27363