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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.

ACKNOWLEDGMENTS National Natural Science Foundation of China (No. 82160275).
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.

[1]
Sun JJ, Li JJ, Dang Y, et al. Advances in gene and clinical diagnosis and treatment of Von Hippel-Lindau syndrome[J]. Northwest Journal of Defense Medicine, 2021, 42(5): 401-407. DOI: 10.16021/j.cnki.1007-8622.2021.05.029.
[2]
Lodi M, Marrazzo A, Cacchione A, et al. Synchronous Presentation of Rare Brain Tumors in Von Hippel-Lindau Syndrome[J] . Diagnostics, 2021, 11(6): 1005. DOI: 10.3390/diagnostics11061005.
[3]
Varshney N, Kebede AA, Owusu-Dapaah H, et al. A Review of Von Hippel-Lindau Syndrome[J]. J Kidney Cancer VHL, 2017, 4: 20-29. DOI: 10.15586/jkcvhl.2017.88.
[4]
Gao HL, Jin KZ, Wang XH, et al. Frequent clinical pathological discussions: pancreatic cyst, intermittent abdominal discomfort[J]. Fudan University Journal of Medical Sciences, 2017, 44(4): 528-531. DOI: 10.3969/j.issn.1672-8467.2017.04.024.
[5]
Zhang L, Fan L, Zou RQ. Imaging manifestations of VHL syndrome[J]. Chinese Imaging Journal of Integrated Traditional and Western Medicine, 2018, 16(3): 286-288. DOI: 10.3969/j.issn.1672-0512.2018.03.020.
[6]
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.
[7]
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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