A Case of Holocord Leptomeningeal Dissemination from Cerebellar Hemangioblastoma without von Hippel-Lindau Disease.

@article{Ohba2017ACO,
  title={A Case of Holocord Leptomeningeal Dissemination from Cerebellar Hemangioblastoma without von Hippel-Lindau Disease.},
  author={Hideo Ohba and Satoshi Yamaguchi and Takuro Magaki and Masaaki Takeda and Manish Kolakshyapati and Takashi Sadatomo and Kaoru Kurisu},
  journal={Hiroshima journal of medical sciences},
  year={2017},
  volume={66 1},
  pages={
          7-10
        }
}
Hemangioblastoma disseminated along leptomeninges from the solitary cranial lesion without von Hippel-Lindau (VHL) disease is a quite rare instance with 23 cases reported in 40 years. We add a new case and discuss these rare instances. A 55-year-old female underwent surgery for total removal of cerebellar hemangioblastoma. Twenty months later, magnetic resonance (MR) images of the spinal cord revealed a tumor compressing the thoracic cord at T3-4 level which was removed en bloc by emergent… CONTINUE READING
2
Twitter Mentions

References

Publications referenced by this paper.
SHOWING 1-10 OF 28 REFERENCES

Postoperative disseminated hemangioblastomatosis without von Hippel-Lindau disease

T. Higuchi, M. Maeda, M. Umino, T. Matsubara, H. Sakuma
  • Jpn. J. Clin. Radiol
  • 2015

Surgical resection of sporadic and hereditary hemangioblastoma: Our 10-year experience and a literature review

E. Bründl, P. Schödel, O. W. Ullrich, A. Brawanski, K. M. Schebesch
  • Surg. Neurol. Int
  • 2014

Similar Papers

Loading similar papers…