Bilateral dysplastic cerebellar gangliocytoma: report of one case and review of the literature

FENG Quan-zhi1; KONG Chui-li2; HAN Tong1

doi:10.12117/jccmi.2020.04.016

Journal of China Clinic Medical Imaging ›› 2020, Vol. 31 ›› Issue (4) : 296-299. DOI: 10.12117/jccmi.2020.04.016

FENG Quan-zhi1, KONG Chui-li2, HAN Tong1

Author information +

History +

Cite this article

EndNote

Ris (Procite)

Bibtex

Download Citations

FENG Quan-zhi1, KONG Chui-li2, HAN Tong1. Bilateral dysplastic cerebellar gangliocytoma: report of one case and review of the literature[J]. Journal of China Clinic Medical Imaging. 2020, 31(4): 296-299 https://doi.org/10.12117/jccmi.2020.04.016

References

[1]L’hermitte J, Duclos P. Sur un ganglioneurome diffus du cortexdu cervelet[J]. Bull Assoc Fr Etud Cancer, 1920, 9: 99-107. [2]Louis DN, Perry A, Reifenberger G, et al. The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary[J]. Acta Neuropathol, 2016, 131(6): 803-820. [3]Puri AS, Garg A, Mishra NK, et al. Bilateral Cerebellar Dysplastic Gangliocytomas(Lhermitte Duclos Disease) with Cerebellar Ectopia and Presyrinx Cord Changes: A Case Report[J]. Neuroradiol J, 2007, 19(6): 717-721. [4]Dutta G, Singh D, Saran RK, et al. Childhood Lhermitte-Duclos disease progressing to medulloblastoma in bilateral cerebellar hemispheres: report of unusual case[J]. World Neurosurg, 2018, 117: 344-349. [5]Bozbuga M, Gulec I, Suslu HT, et al. Bilateral Lhermitte-Duclos disease[J]. Neurol India, 2010, 58(2): 309-311. [6]张宗军，季学满，吴波，等. 小脑发育不良性节细胞瘤的CT和MRI诊断（4例报告及文献复习）[J]. 中国临床医学影像杂志，2009，20（3）：197-200. [7]Marsh DJ, Coulon V, Lunetta KL, et al. Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation[J]. Hum Mol Genet, 1998, 7(3): 507-515. [8]Jain N, Chauhan U, Goel V, et al. Lhermitte-Duclos Disease: Diagnosis on MRI, MR Spectroscopy, CT and Positron Emission Tomography[J]. J Clin Diagn Res, 2015, 9(9): 1-2. [9]Robinson S, Cohen AR. Cowden disease and Lhermitte-Duclos disease: characterization of a new phakomatosis[J]. Neurosurgery, 2000, 46(2): 371-383. [10]Hulcelle P, Dooms G, Vermonden J. Lhermitte-Duclos disease. A case report[J]. J Neuroradiol, 1994, 21(1): 40-45. [11]Buhl R, Barth H, Hugo HH, et al. Dysplastic gangliocytoma of the cerebellum: rare differential diagnosis in space occupying lesions of the posterior fossa[J]. Acta Neurochir(Wien), 2003, 145(6): 509-512. [12]林欣，潘隆盛，余新光. 小脑发育不良性神经节细胞瘤[J]. 中国临床神经外科杂志，2005，10（2）：150-152. [13]袁菊，吴楠，王璇，等. 小脑发育不良性节细胞瘤/Lhermitte-Duclos病6例临床病理分析并文献复习[J]. 临床与实验病理学杂志，2017，33（9）：1001-1004. [14]Nair P, Pal L, Jaiswal AK, et al. Lhermitte-Duclos disease associated with dysembryoplastic neuroepithelial tumor differentiation with characteristic magnetic resonance appearance of “Tiger Striping”[J]. World Neurosurg, 2011, 75(5-6): 699-703. [15]Ma J, Jia G, Chen S, et al. Clinical Perspective on Dysplastic gangliocytoma of the cerebellum(Lhermitte-Duclos disease)[J]. World Neurosurg, 2019, 122: 16-23. [16]郑丽丽，赵庆雪，王巍，等. 小脑发育不良性神经节细胞瘤MRI表现及临床病理分析[J]. 中华放射学杂志，2014，48（12）：1051-1052. [17]Awwad EE, Levy E, Martin DS, et al. Atypical MR appearance of Lhermitte-Duclos disease with contrast enhancement[J]. AJNR, 1995, 16(8): 1719-1720. [18]Spaargaren L, Cras P, Bomhof MAM, et al. Contrast enhancement in Lhermitte-Duclos disease of the cerebellum: correlation of imaging with neuropathology in two cases[J]. Neuroradiology, 2003, 45(6): 381-385. [19]Thomas B, Krishnamoorthy T, Radhakrishnan VV, et al. Advanced MR imaging in Lhermitte-Duclos disease: moving closer to pathology and pathophysiology[J]. Neuroradiology, 2007, 49(9): 733-738. [20]Gaballo A, Palma M, Dicuonzo F, et al. Lhermitte-Duclos disease: MR diffusion and spectroscopy[J]. Radiol Med, 2005, 110(4): 378-384. [21]Ogasawara K, Yasuda S, Beppu T, et al. Brain PET and technetium-99m-ECD SPECT imaging in Lhermitte-Duclos disease[J]. Neuroradiology, 2001, 43(11): 993-996. [22]Klisch J, Juengling F, Spreer J, et al. Lhermitte-Duclos disease: assessment with MR imaging, positron emission tomography, single-photon emission CT, and MR spectroscopy[J]. AJNR, 2001, 22(5): 824-830. [23]王琼，高培毅，林燕，等. 非小脑蚓部髓母细胞瘤的CT和MRI表现[J]. 放射学实践，2012，27（10）：1058-1060. [24]方庆和，刘世忠，庄楠，等. 胚胎发育不良性神经上皮肿瘤附6例病例分析[J]. 医学影像学杂志，2013，23（5）：669-671. [25]杨蕊梦，江新青，许乙凯. 颅内神经节细胞胶质瘤的MRI表现[J]. 放射学实践，2011，26（3）：278-281. [26]Murahashi T, Sato K, Ito T, et al. A case of pilocytic astrocytoma in an adult[J]. No Shinkei Geka, 2012, 40(9): 793-797. [27]刘干辉，程英，陈振松，等. 小脑发育不良性节细胞瘤的影像诊断与鉴别诊断[J]. 临床放射学杂志，2013，32（5）：623-626. [28]Bhatia JK, Bhatoe HS, Vadhanan S. Lhermitte-Duclos disease: A rare entity[J]. Med J Armed Forces India, 2016, 72(Suppl 1): S147-S149. [29]Zak M, Ledbetter M, Maertens P. Infantile Lhermitte-Duclos Disease Treated Successfully With Rapamycin[J]. J Child Neurol, 2017, 32(3): 322-326.