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Bilateral Recurrent Dysplastic Cerebellar Gangliocytoma (Lhermitte-Duclos Disease) in Cowden Syndrome: A Case Report and Literature Review.双侧复发性小脑神经节细胞瘤(Lhermitte-Duclos 病)合并考登综合征:病例报告及文献复习。
World Neurosurg. 2019 Jul;127:319-325. doi: 10.1016/j.wneu.2019.03.131. Epub 2019 Mar 21.
3
Lhermitte-Duclos disease: Clinical study with long-term follow-up in a single institution.莱尔米特-迪克洛病:单机构长期随访的临床研究
Clin Neurol Neurosurg. 2017 Nov;162:53-58. doi: 10.1016/j.clineuro.2017.09.007. Epub 2017 Sep 9.
4
Lhermitte-Duclos Disease Treated Surgically in an Elderly Patient: Case Report and Literature Review.老年患者手术治疗的Lhermitte-Duclos病:病例报告及文献综述
Turk Neurosurg. 2015;25(5):783-7. doi: 10.5137/1019-5149.JTN.9835-13.2.
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MR Spectroscopy Findings in Lhermitte-Duclos Disease. A Case Report.Lhermitte-Duclos病的磁共振波谱分析结果:一例报告
Neuroradiol J. 2007 Jun 30;20(3):278-81. doi: 10.1177/197140090702000304.
6
A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands.提出了一种基于 3042 名先证者前瞻性研究的临床评分系统,用于选择进行 PTEN 基因突变检测的患者。
Am J Hum Genet. 2011 Jan 7;88(1):42-56. doi: 10.1016/j.ajhg.2010.11.013. Epub 2010 Dec 30.
7
Anaplastic ganglioglioma arising from a Lhermitte-Duclos-like lesion. Case report.起源于类Lhermitte-Duclos病变的间变性节细胞胶质瘤。病例报告。
J Neurosurg. 2007 Aug;107(2 Suppl):137-42. doi: 10.3171/PED-07/08/137.
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Ectopic recurrence of dysplastic gangliocytoma of the cerebellum (Lhermitte-Duclos disease): a case report.小脑发育异常性神经节细胞瘤(Lhermitte-Duclos病)的异位复发:一例报告
Brain Tumor Pathol. 2007;24(1):25-9. doi: 10.1007/s10014-006-0211-z. Epub 2007 May 25.
9
Advanced MR imaging in Lhermitte-Duclos disease: moving closer to pathology and pathophysiology.Lhermitte-Duclos病的高级磁共振成像:更接近病理学和病理生理学
Neuroradiology. 2007 Sep;49(9):733-8. doi: 10.1007/s00234-007-0241-1. Epub 2007 Jun 5.
10
Lhermitte-Duclos disease.勒米特-迪克洛病
Childs Nerv Syst. 2007 Jul;23(7):729-32. doi: 10.1007/s00381-006-0271-8. Epub 2007 Jan 13.

Lhermitte-Duclos 病:一例病例报告及文献复习。

Lhermitte-Duclos disease: A case report and literature review.

机构信息

Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha 410008.

Grade of 2015 in Oral Medicine, Medical College of Jinzhou Medical University, Jinzhou Liaoning 121001, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2021 Feb 28;46(2):195-199. doi: 10.11817/j.issn.1672-7347.2021.190574.

DOI:10.11817/j.issn.1672-7347.2021.190574
PMID:33678658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10929790/
Abstract

Lhermitte-Duclos disease (LDD) is a type of rare brain tumor located in posterior fossa. A patient with LDD located in the left cerebellum and vermis was admitted by the Department of Neurosurgery, Xiangya Hospital, Central South University. MRI scan showed slightly heterogeneous enhancement at the region close to vermis. The patient underwent partial resection on August 11, 2016 without postoperative chemoradiotherapy. The progress free survival was 11 months and the overall survival was 17 months. What the case reveals is that the partial resection is not beneficial to these patients with LDD as the residual lesion probably recurs in a short term after operation. The pathogenesis, diagnosis and treatment of LDD are explored and summarized in combination with relevant literature.

摘要

Lhermitte-Duclos 病(LDD)是一种位于后颅窝的罕见脑肿瘤。中南大学湘雅医院神经外科收治了一名位于左小脑和蚓部的 LDD 患者。MRI 扫描显示蚓部附近区域呈轻度异质性增强。该患者于 2016 年 8 月 11 日接受了部分切除术,术后未进行放化疗。无进展生存期为 11 个月,总生存期为 17 个月。该病例揭示了部分切除术对 LDD 患者无益,因为残余病变在术后短期内可能会复发。结合相关文献,探讨并总结了 LDD 的发病机制、诊断和治疗。