{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,9]],"date-time":"2026-04-09T13:45:46Z","timestamp":1775742346246,"version":"3.50.1"},"reference-count":26,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2015,10,9]],"date-time":"2015-10-09T00:00:00Z","timestamp":1444348800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Aust Veterinary J"],"published-print":{"date-parts":[[2015,12]]},"abstract":"<jats:sec><jats:title>Case report<\/jats:title><jats:p>An 8\u2010year\u2010old spayed female cross\u2010breed dog was evaluated following a 2\u2010month history of thoracic limb weakness. Neurological examination revealed a spinal cord lesion between C1 and C5 segments. Magnetic resonance imaging (MRI) revealed that almost 70% of the spinal canal between C1 and C2 was occupied by an intradural extramedullary mass that was connected to a paraspinal mass from the cranial aspect of C2 to the cranial aspect of C3. The dog was anaesthetised and a dorsal, right\u2010sided hemilaminectomy was performed. A durotomy was performed to expose a multilobular mass located principally along the right dorsal\u2013lateral aspect of the spinal cord. The mass did not appear to infiltrate the cord parenchyma. The abnormal tissue was removed as completely as possible using gentle dissection and submitted for histological evaluation. The histological findings were consistent with an intradural\u2013extramedullary haemangioblastoma with paraspinal extension. Following surgery, no neurological deterioration was detected. A metronomic\u2010dosing chemotherapy protocol was administered to prevent progression or recurrence of the tumour. Follow\u2010up MRI studies were performed 3, 6 and 12\u2009months after the surgery, confirming complete tumour removal and the absence of recurrence.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Haemangioblastoma is an extremely rare neoplasm in animals and only two cases of this tumour have been reported, but in other anatomical locations. Haemangioblastomas in human patients are more commonly located in the cerebellum and intradural\u2013extramedullary growth is extremely rare. The dog in this study responded favourably to combined surgery and metronomic chemotherapy and was clinically normal 1\u2009year after surgery.<\/jats:p><\/jats:sec>","DOI":"10.1111\/avj.12376","type":"journal-article","created":{"date-parts":[[2015,10,9]],"date-time":"2015-10-09T07:49:42Z","timestamp":1444376982000},"page":"460-465","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":12,"title":["Intradural\u2013extramedullary haemangioblastoma with paraspinal extension in a dog"],"prefix":"10.1111","volume":"93","author":[{"given":"D","family":"Binanti","sequence":"first","affiliation":[{"name":"Veterinary University Hospital, School of Veterinary Medicine Universit\u00e0 degli Studi di Milano  Milan Italy"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D","family":"De Zani","sequence":"additional","affiliation":[{"name":"Veterinary University Hospital, School of Veterinary Medicine Universit\u00e0 degli Studi 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