Progressive Spinal and Cerebellar Multifocal Hemangioblastoma in Von Hippel-Lindau Disease: Case Report and Literature Review

Although cerebellar hemangioblastoma is histologically benign, it can exhibit malignant clinical behavior during long-term follow-up. This report presents the case of a 51-year-old male with von Hippel-Lindau (VHL) disease, characterized by multifocal hemangioblastomas in the spine and cerebellum, as well as multiple cystic lesions in the kidneys and pancreas. The patient underwent nine surgeries for recurrent cerebellar hemangioblastomas and received cranial radiotherapy for multiple intracranial masses. Additionally, he was diagnosed with and treated for renal cell carcinoma arising from a renal cyst. This case highlights the potential for cerebellar hemangioblastoma recurrence and malignant progression of associated lesions in VHL disease, even after complete resection.

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Publication Details

Journal
Nepal Journal of Neuroscience
Published
2025-09-29
DOI
https://doi.org/10.3126/njn.v22i2.74636
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
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article

Progressive Spinal and Cerebellar Multifocal Hemangioblastoma in Von Hippel-Lindau Disease: Case Report and Literature Review

Lan Duong Thi Ngoc, Vinh-Lac Nguyen, Minh Thien Nguyen, Dinh Thi Phuong Hoai et al.
Nepal Journal of Neuroscience
Cancer, Hypoxia, and Metabolism
article

Progressive Spinal and Cerebellar Multifocal Hemangioblastoma in Von Hippel-Lindau Disease: Case Report and Literature Review

Lan Duong Thi Ngoc, Vinh-Lac Nguyen, Minh Thien Nguyen, Dinh Thi Phuong Hoai, Christine Le, Yukari Kato, Hanh Thi Kieu Le, Tien N. T. Nguyen, Hien Q. Huynh, Hoang D. Tran, Vilatda Moungkhounsin
article en

Abstract

Although cerebellar hemangioblastoma is histologically benign, it can exhibit malignant clinical behavior during long-term follow-up. This report presents the case of a 51-year-old male with von Hippel-Lindau (VHL) disease, characterized by multifocal hemangioblastomas in the spine and cerebellum, as well as multiple cystic lesions in the kidneys and pancreas. The patient underwent nine surgeries for recurrent cerebellar hemangioblastomas and received cranial radiotherapy for multiple intracranial masses. Additionally, he was diagnosed with and treated for renal cell carcinoma arising from a renal cyst. This case highlights the potential for cerebellar hemangioblastoma recurrence and malignant progression of associated lesions in VHL disease, even after complete resection.

Nepal Journal of NeuroscienceVol. 22(2)
Fujita Health University (JP), Hue University (VN)
Openalex Percentile: Top 67%
Cancer, Hypoxia, and Metabolism
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Progressive Spinal and Cerebellar Multifocal Hemangioblastoma in Von Hippel-Lindau Disease: Case Report and Literature Review — Lan Duong Thi Ngoc, Vinh-Lac Nguyen, et al. · Nepal Journal of Neuroscience (2025) | TGRS Research Map | TGRS