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Case Report
Image manifestations of typical Von Hippel-Lindau syndrome: One case report
SHI Yaoping  XU Ziwei  MO Yin  XUN Rui 

Cite this article as: Shi YP, Xu ZW, Mo Y, et al. Image manifestations of typical Von Hippel-Lindau syndrome: One case report[J]. Chin J Magn Reson Imaging, 2022, 13(2): 97-98. DOI:10.12015/issn.1674-8034.2022.02.021.


[Keywords] Von Hippel-Lindau syndrome;hemangioblastoma;magnetic resonance imaging;computed tomography

SHI Yaoping1   XU Ziwei1   MO Yin1*   XUN Rui2  

1 Department of Medical Imaging, the First Affiliated Hospital of Kunming Medical University, Kunming 650000, China

2 Armed Police Yunnan Provincial Corps Hospital, Kunming 650000, China

Mo Yin, E-mail: 13888905910@163.com

Conflicts of interest   None.

Received  2021-08-11
Accepted  2021-11-25
DOI: 10.12015/issn.1674-8034.2022.02.021
Cite this article as: Shi YP, Xu ZW, Mo Y, et al. Image manifestations of typical Von Hippel-Lindau syndrome: One case report[J]. Chin J Magn Reson Imaging, 2022, 13(2): 97-98.DOI:10.12015/issn.1674-8034.2022.02.021

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Crossey PA, Eng C, Ginalska-Malinowska M, et al. Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma[J]. J Med Genet, 1995, 32: 885-886. DOI: 10.1136/jmg.32.11.885.
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Cui H, Zou J, Bao YH, et al. Surgical treatment of solid hemangioblastomas of the posterior fossa: A report of 28 cases[J]. Oncol Lett, 2017, 13: 1125-1130. DOI: 10.3892/ol.2016.5531.

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