Unusual Spinal Foraminal Hemangioblastoma With Prominent Arteriovenous Shunt

Von Hippel-Lindau (VHL) disease is a rare neurocutaneous disorder characterized by multiple benign and malignant tumors involving different organs (renal, adrenal, pancreas, liver, urogenital system, central nervous system, and head and neck region) due to mutations in the VHL tumor suppressor gene....

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Veröffentlicht in:Curēus (Palo Alto, CA) CA), 2023-09, Vol.15 (9)
Hauptverfasser: Santos, Mariana, Marussi, Victor H, Campos, Christiane M, Doria-Netto, Hugo Leonardo, Doria-Netto, Ricardo Henrique, Chaddad-Neto, Feres, Amaral, Lázaro Luís F
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Sprache:eng
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Zusammenfassung:Von Hippel-Lindau (VHL) disease is a rare neurocutaneous disorder characterized by multiple benign and malignant tumors involving different organs (renal, adrenal, pancreas, liver, urogenital system, central nervous system, and head and neck region) due to mutations in the VHL tumor suppressor gene. Here, we describe a patient with unknown VHL disease who has complained of hypoesthesia of the right lower limb for about six years. A lumbar MRI was performed and revealed an expansive foraminal lesion at the right L3-L4 level and multiple serpiginous intradural and extramedullary flow voids involving the dorsal aspect of the spinal cord. The patient underwent digital subtraction angiography to exclude a spinal dural arteriovenous fistula, which revealed imaging features suggestive of spinal hemangioblastoma. In the presence of a spinal hemangioblastoma, a brain MRI was performed for further evaluation to rule out the possible diagnosis of VHL disease, and a solitary hemangioblastoma on the right cerebellar hemisphere was found. The patient underwent lumbar spine surgery, confirming the suspicious diagnosis of hemangioblastomas related to VHL disease.
ISSN:2168-8184
2168-8184
DOI:10.7759/cureus.46205