The Lhermitte-Duclos disease: a rare bilateral cerebellar location of a rare pathology
نویسندگان
چکیده
منابع مشابه
Lhermitte – Duclos Disease in a Young Adult: Rare Entity
Lhermitte - Duclos disease also called dysplastic gangliocytoma of cerebellum is an extremely rare cerebellar lesion which share features of both malformation and neoplasm. The usual presentation is of raised intracranial pressure along with cerebellar signs. We report a case of 23 year male who presented with headache & diplopia. MRI was suggestive of the diagnosis. Subtotal excision of th...
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A 42-year-old female presented with complaints of mild occipital headaches of severe months duration. There were no cutaneous lesions or significant family history suggesting any genetic disease. On examination, she did not have any papilloedema, dymetria, dysdiadokokinasia or ataxia. Her cranial nerve examination was normal. On non-enhanced computed tomogram (CT) showed a mildly hyperdense wel...
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A 57-year-old woman with a history of hypothyroidism, hysterectomy and depression presented to the emergency department (ED) with 3 months of progressive vertigo, ataxia and posterior headache. The patient denied fever, weight loss, vision difficulty or trauma. The patient was directed to the ED because of an abnormal outpatient MRI done earlier that day obtained by her family physician. The pa...
متن کاملLhermitte-duclos Disease-intraoperative Cytological Findings of a Rare Entity
OBJECTIVE: A rare case of LDD confirmed by biopsy is being reported. Review of the published cases shows that the disease usually manifests by the signs of increased intracranial pressure with inconstant cerebellar symptoms. MRI is the imaging modality of choice by now. As such, clinical problems after gross total or complete removal have not been reported so far, but herein we stress the impor...
متن کاملlhermitte – duclos disease in a young adult: rare entity
lhermitte - duclos disease also called dysplastic gangliocytoma of cerebellum is an extremely rare cerebellar lesion which share features of both malformation and neoplasm. the usual presentation is of raised intracranial pressure along with cerebellar signs. we report a case of 23 year male who presented with headache & diplopia. mri was suggestive of the diagnosis. subtotal excision of th...
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ژورنال
عنوان ژورنال: Pan African Medical Journal
سال: 2019
ISSN: 1937-8688
DOI: 10.11604/pamj.2019.33.118.16809