Complete regression of intracranial arteriovenous malformations.
Publication/Presentation Date
8-1-2002
Abstract
BACKGROUND: Spontaneous and complete regression of intracranial arteriovenous malformations (AVMs) is a rare occurrence, with only 59 angiographically proven cases reported in the English literature. We present three new cases and perform a literature review to determine possible mechanisms underlying this unusual phenomenon.
METHODS: Three patients with angiographically proven AVMs demonstrated complete obliteration of the AVM on follow-up angiography. Two patients had MRIs performed at the time of follow-up angiography.
RESULTS: A literature review of all reported cases shows that the vast majority (88%) of spontaneously closing AVMs had a single draining vein as did our three cases. In addition, hemodynamic alterations of intracranial (IC) blood flow, including intracranial hemorrhage, were seen in a majority (79%) of patients, including two of our three cases. MRI was performed in two of our three cases and showed a thrombosed-draining vein in both.
CONCLUSIONS: Complete spontaneous regression of intracranial AVMs is a rare occurrence. The phenomenon seems to require the interaction of hemodynamic changes in compromising or closing the limited, usually single, venous drainage pathway from the AVM. Hemorrhage may contribute to the effect by further compromising flow though the lesion, or it may merely be a phenomenon associated with the effects of venous hypertension on the AVM nidus.
Volume
58
Issue
2
First Page
139
Last Page
147
ISSN
0090-3019
Published In/Presented At
Schwartz, E. D., Hurst, R. W., Sinson, G., & Bagley, L. J. (2002). Complete regression of intracranial arteriovenous malformations. Surgical neurology, 58(2), 139–147. https://doi.org/10.1016/s0090-3019(02)00769-3
Disciplines
Diagnosis | Medicine and Health Sciences | Other Analytical, Diagnostic and Therapeutic Techniques and Equipment | Radiology
PubMedID
12453655
Department(s)
Department of Radiology and Diagnostic Medical Imaging
Document Type
Article