| Literature DB >> 27654743 |
Cemile Ayse Gormeli1, Kaya Sarac2, Zeynep Maras Ozdemir2, Gokay Gormeli3, Aysegul Sagir Kahraman2, Bayram Kahraman2, Mustafa Namik Oztanir4, Nese Karadag5.
Abstract
Spinal 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.Entities:
Keywords: Spinal cord haemangioblastoma, Haemorrhage, Paraplegia, Magnetic resonance.zzm321990
Mesh:
Year: 2016 PMID: 27654743
Source DB: PubMed Journal: J Pak Med Assoc ISSN: 0030-9982 Impact factor: 0.781