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Spinal hemangioblastomas are the third most common intramedullary spinal neoplasm, representing 2-6% of all intramedullary tumors 1,4,7.
This article specifically relates to spinal hemangioblastomas. For a discussion on intracranial hemangioblastomas and a general discussion of the pathology refer to the main article: hemangioblastoma.
Hemangioblastomas are mostly sporadic (two-thirds) with a peak presentation in the fourth decade. Sporadic hemangioblastomas only rarely occur in children. Males and females are affected equally 4,7.
One-third of patients with hemangioblastomas (not just spinal) have von Hippel-Lindau syndrome 6,7 and typically these patients present earlier with multiple tumors.
Clinical presentation is similar to that of other intramedullary spinal tumors, with pain, weakness and sensory changes common. Rarely, spinal hemangioblastomas may cause subarachnoid hemorrhage or hematomyelia 4.
Hemangioblastomas are benign vascular lesions that do not undergo malignant degeneration. They are WHO grade 1 in the 5th Edition (2021) of the WHO classification of CNS tumors 9.
Histologically, they consist of large pale stromal cells packed between blood vessels.
The most common location is the thoracic cord (50%), followed by the cervical cord (40%) 4,7. The majority of hemangioblastomas have an intramedullary component with two-thirds located eccentrically and having an exophytic component (most commonly along the dorsum of the cord 8). Only 25% are entirely intramedullary. A minority appears entirely extramedullary and only rarely are they extradural 2,7.
Eighty percent of hemangioblastomas are solitary. If multiple lesions are present, von Hippel-Lindau syndrome should be suspected 4.
A densely enhancing nidus with associated dilated arteries and prominent draining veins is characteristic of a hemangioblastoma.
On non-contrast CT they may be seen as a soft tissue nodule often with a prominent hypodense cyst-like component. Contrast administration results in vivid enhancement of the solid component.
Although they usually appear as discrete nodules, there can be diffuse cord expansion. An associated tumor cyst or syrinx is common (50-100%) 2,4. Additionally, they may rarely be a source of subarachnoid hemorrhage or hematomyelia 4,7.
Reported signal characteristics of the solid components include 4,7:
- variable relative to the normal spinal cord
- hypo- to isointense most common, and difficult to identify
- hyperintense (25%)
- iso- to hyperintense
- focal flow voids especially in larger lesions
- surrounding edema and associated syrinx are usually seen
- hemosiderin capping may be present
T1 C+ (Gd)
- the tumor nodule enhances vividly
Care should be taken to image the whole neuraxis to ensure that no other lesions are present.
Treatment and prognosis
Hemangioblastomas are slow-growing. They are usually treated by surgical resection, sometimes with preceding endovascular embolization to reduce intraoperative blood loss.
The differential diagnosis can be thought of in two groups on account of the principal features of these tumors: neoplasms of the spinal canal (enhancing component) and vascular malformations of the spinal cord (enlarged vessels)
Other enhancing masses to be considered include:
- intradural extramedullary tumors
- intramedullary spinal cord tumors
Vascular malformation to consider include:
- 1. Brant WE, Helms CA. Fundamentals of Diagnostic Radiology. Lippincott Williams & Wilkins. (2007) ISBN:0781761352. Read it at Google Books - Find it at Amazon
- 2. Osborn AG. Diagnostic neuroradiology. Mosby Inc. (1994) ISBN:0801674867. Read it at Google Books - Find it at Amazon
- 3. Grossman RI, Yousem DM. Neuroradiology, the requisites. Mosby Inc. (2003) ISBN:032300508X. Read it at Google Books - Find it at Amazon
- 4. Koeller KK, Rosenblum RS, Morrison AL. Neoplasms of the spinal cord and filum terminale: radiologic-pathologic correlation. Radiographics. 20 (6): 1721-49. Radiographics (citation) - Pubmed citation
- 5. Smith AB, Soderlund KA, Rushing EJ et-al. Radiologic-pathologic correlation of pediatric and adolescent spinal neoplasms: Part 1, Intramedullary spinal neoplasms. AJR Am J Roentgenol. 2012;198 (1): 34-43. doi:10.2214/AJR.10.7311 - Pubmed citation
- 6. Abul-kasim K, Thurnher MM, Mckeever P et-al. Intradural spinal tumors: current classification and MRI features. Neuroradiology. 2008;50 (4): 301-14. doi:10.1007/s00234-007-0345-7 - Pubmed citation
- 7. Baker KB, Moran CJ, Wippold FJ et-al. MR imaging of spinal hemangioblastoma. AJR Am J Roentgenol. 2000;174 (2): 377-82. AJR Am J Roentgenol (citation) - Pubmed citation
- 8. Chu BC, Terae S, Hida K et-al. MR findings in spinal hemangioblastoma: correlation with symptoms and with angiographic and surgical findings. AJNR Am J Neuroradiol. 2001;22 (1): 206-17. AJNR Am J Neuroradiol (citation) - Pubmed citation
- 9. Tihan T, Fanburg-Smith J, Vortmeyer AO, Zagzag D, Haemangioblastoma. In: WHO Classification of Tumours Editorial Board. Central nervous system tumours. Lyon (France): International Agency for Research on Cancer; 2021. (WHO classification of tumours series, 5th ed.; vol. 6). https://publications.iarc.fr/601