Spontaneous regression of cerebral arteriovenous malformations: clinical and angiographic analysis with review of the literature
- 1. Department of Medical Imaging, Toronto Western Hospital, Toronto, ON (Canada)
Description
Spontaneous regression of cerebral arteriovenous malformation (AVM) is rare and poorly understood. We reviewed the clinical and angiographic findings in patients who had spontaneous regression of cerebral AVMs to determine whether common features were present. The clinical and angiographic findings of four cases from our series and 29 cases from the literature were retrospectively reviewed. The clinical and angiographic features analyzed were: age at diagnosis, initial presentation, venous drainage pattern, number of draining veins, location of the AVM, number of arterial feeders, clinical events during the interval period to thrombosis, and interval period to spontaneous thrombosis. Common clinical and angiographic features of spontaneous regression of cerebral AVMs are: intracranial hemorrhage as an initial presentation, small AVMs, and a single draining vein. Spontaneous regression of cerebral AVMs can not be predicted by clinical or angiographic features, therefore it should not be considered as an option in cerebral AVM management, despite its proven occurrence. (orig.)
Additional details
Identifiers
Publishing Information
- Journal Title
- Neuroradiology
- Journal Volume
- 44
- Journal Issue
- 1
- Journal Page Range
- p. 11-16
- ISSN
- 0028-3940
- CODEN
- NRDYAB
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 33011674
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BIOMEDICAL RADIOGRAPHY; BLOOD VESSELS; CARDIOVASCULAR DISEASES; CONGENITAL MALFORMATIONS; REVIEWS; THROMBOSIS
- Descriptors DEC
- BODY; CARDIOVASCULAR DISEASES; CARDIOVASCULAR SYSTEM; DIAGNOSTIC TECHNIQUES; DISEASES; DOCUMENT TYPES; MALFORMATIONS; MEDICINE; NUCLEAR MEDICINE; ORGANS; PATHOLOGICAL CHANGES; RADIOLOGY; VASCULAR DISEASES
Optional Information
- Notes
- 10.1007/s002340100702