Cerebellar developmental venous anomaly with associated cavernoma causing a hemorrhage – a rare occurrence

Autor: Omar Marzouk, BSc (Hons), MUDr, Sherief Marzouk, BSc, MBBS, MRCS, Do-HNS, Sidath H. Liyanage, BSc (Hons), MBBS, MRCS, Do-HNS, FRCR, PgC Med Ed, Iris Q Grunwald, MD, PhD
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Zdroj: Radiology Case Reports, Vol 16, Iss 6, Pp 1463-1468 (2021)
Druh dokumentu: article
ISSN: 1930-0433
DOI: 10.1016/j.radcr.2021.03.010
Popis: Developmental venous anomalies (DVAs) are variations in the transmedullary veins required for drainage of the brain. Normally, when occurring in isolation, DVAs are not clinically significant and are therefore usually a benign diagnosis. Thus, they are most often an incidental finding unless associated with an adjacent pathology. However, intracranial haemorrhage induced by a DVA alone can rarely occur and has been scarcely reported. In this case report we discuss a 58-year-old woman who presented with signs and symptoms of a cerebellar syndrome. Following a non-contrast CT, a CT angiogram and MRI contrast scan of the brain, she was found to have a cerebellar DVA and an intracranial haemorrhage. Subsequent imaging 3 months later with CT and MRI redemonstrated additional evidence of a cavernoma. The patient was managed conservatively.
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