Gormeli, Cemile AyseSarac, KayaOzdemir, Zeynep MarasGormeli, GokayKahraman, Aysegul SagirKahraman, BayramOztanir, Mustafa Namik2024-08-042024-08-0420160030-9982https://hdl.handle.net/11616/97457Spinal cord haemangioblastomas are rare central nervous systems tumours, and haemorrhage. It is an uncommon occurance. We report a 28-year-old pregnant patient who presented with paraplegia due to acute haemorrhage of a spinal haemangioblastoma. Magnetic resonance imaging showed extensive syrinx cavities, an intramedullary lesion at the T4-T5 spinal cord level e, and a subarachnoid haemorrhage. Digital subtraction angiography showed the feeding artery and dilated tortuous draining vein within the dural sac. The lesion was deemed a haemangioblastoma. The histopathological examination confirmed the diagnosis. Postoperatively, the paraplegia improved and the patient was able to walk within 2 weeks. Imaging is important for early diagnosis to prevent patients persistent neurological deficits.eninfo:eu-repo/semantics/closedAccessSpinal cord haemangioblastomaHaemorrhageParaplegiaMagnetic resonanceEditorial66911821184276547432-s2.0-84981354102Q4WOS:000386138300029Q4