Literature DB >> 21704939

Lhermitte-Duclos disease associated with dysembryoplastic neuroepithelial tumor differentiation with characteristic magnetic resonance appearance of "tiger striping".

Prakash Nair1, Lily Pal, Awadhesh K Jaiswal, Sanjay Behari.   

Abstract

BACKGROUND: The simultaneous presence of Lhermitte-Duclos disease (LDD) with focal areas of nodular dysembryoplastic neuroepithelial tumor (DNET) differentiation in the cerebellar hemisphere is reported in a patient who showed the characteristic magnetic resonance imaging (MRI) appearance of "tiger striping". CASE REPORT: A 25-year-old man presented with a 7-month history of holocranial headache, progressive vision diminution, and right-sided cerebellar signs. Computed tomography (CT) scan revealed a hypodense, nonenhancing right cerebellar lesion effacing the fourth ventricle. There were thin hyperdense, linear striations across the tumor with hypodense streaks between them. The third and lateral ventricles were dilated with periventricular lucency. MRI showed the hypointense-to-isointense right cerebellar lesion with linear striations on T1-weighted images. The lesion was hyperintense on T2-weighted images with areas of linear hypointensity streaks running throughout the lesion characteristic of the "tiger striping" effect of LDD. Sagittal MRI revealed tonsillar herniation. Gross total removal of the tumor was accomplished with right paramedian suboccipital craniectomy. The postoperative course was unremarkable, and the patient remained symptom-free at 3-month follow-up examination. Histology revealed the simultaneous presence of LDD with DNET.
CONCLUSIONS: To the best of the authors' knowledge, the simultaneous presence of cerebellar LDD with DNET has never been reported before. This case report may point to their common genesis with cortical dysplasia and neuronal migrational abnormalities playing an important role. LDD and DNET may represent different points in the spectrum of the lesion-from being purely hamartomatous to having a greater proliferative potential. The simultaneous presence of LDD and DNET was perhaps responsible for the unusually rapid neurologic deterioration in this patient before surgical intervention.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21704939     DOI: 10.1016/j.wneu.2010.10.046

Source DB:  PubMed          Journal:  World Neurosurg        ISSN: 1878-8750            Impact factor:   2.104


  6 in total

1.  Uncommon low-grade brain tumors.

Authors:  Thankamma Ajithkumar; Naduni Imbulgoda; Elliott Rees; Fiona Harris; Gail Horan; Amos Burke; Sarah Jefferies; Stephen Price; Justin Cross; Kieren Allinson
Journal:  Neuro Oncol       Date:  2019-02-14       Impact factor: 12.300

2.  Acute-onset cerebellar symptoms in Lhermitte-Duclos disease: case report.

Authors:  Omid R Hariri; Arsineh Khachekian; Dan Muilli; Jenny Amin; Tanya Minassian; Blake Berman; Yoav Ritter; Javed Siddiqi
Journal:  Cerebellum       Date:  2013-02       Impact factor: 3.847

Review 3.  Similar MR imaging characteristics but different pathological changes: a misdiagnosis for Lhermitte-Duclos disease and review of the literature.

Authors:  Shengyue Huang; Guobin Zhang; Junting Zhang
Journal:  Int J Clin Exp Pathol       Date:  2015-06-01

4.  Management of unusual dysplastic gangliocytoma of the cerebellum (Lhermitte-Duclos disease) in a developing country: Case report and review of the literature.

Authors:  Nyoman Golden; Mahadewa G B Tjokorda; Maliawan Sri; Wayan Niryana; Saputra Herman
Journal:  Asian J Neurosurg       Date:  2016 Apr-Jun

Review 5.  Signs in Neuroradiology: A Pictorial Review.

Authors:  Özgür Kizilca; Alp Öztek; Uğur Kesimal; Utku Şenol
Journal:  Korean J Radiol       Date:  2017-09-21       Impact factor: 3.500

6.  Complex form variant of dysembryoplastic neuroepithelial tumor of the cerebellum.

Authors:  Jesús Vaquero; Cristobal Saldaña; Santiago Coca; Mercedes Zurita
Journal:  Case Rep Pathol       Date:  2012-09-05
  6 in total

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