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British Journal of Neurosurgery Volume 29, 2015 - Issue 2
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Metastatic pancreatic neuroendocrine tumor to the central nervous system in a patient with von Hippel–Lindau disease: A case report and literature review

Matthew R. ReynoldsDepartment of Neurological Surgery, Washington University in St. Louis, St. Louis, MO, USA;Department of Neurological Surgery, Beaumont Hospital, Dublin, Republic of IrelandCorrespondence[email protected]
,
Shane M. CrillyDepartment of Neurological Surgery, Beaumont Hospital, Dublin, Republic of Ireland
,
Kieron J. SweeneyDepartment of Neurological Surgery, Beaumont Hospital, Dublin, Republic of Ireland
,
Michael FarrellDepartment of Neurological Surgery, Beaumont Hospital, Dublin, Republic of Ireland;Department of Neuropathology, Beaumont Hospital, Dublin, Republic of Ireland
&
Daniel RawlukDepartment of Neurological Surgery, Beaumont Hospital, Dublin, Republic of Ireland
Pages 291-293 | Received 07 Apr 2014, Accepted 19 Aug 2014, Published online: 18 Sep 2014

References

  • Blansfield JA, Choyke L, Morita SY, et al. Clinical, genetic and radiographic analysis of 108 patients with von Hippel-Lindau disease (VHL) manifested by pancreatic neuroendocrine tumors (PNETs). Surgery 2007;142:814–8.e1–2.
  • Jarrell ST, Vortmeyer AO, Linehan WM, Oldfield EH, Lonser RR. Metastases to hemangioblastomas in von Hippel-Lindau disease. J Neurosurg 2006;105:256–63.

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