TY - CHAP
T1 - Arteriovenous Malformations
T2 - Treatment and Management
AU - Rahme, Rudy J.
AU - Singh, Rohin
AU - De La Pena, Nicole
AU - Turcotte, Evelyn L.
AU - Bendok, Bernard R.
N1 - Publisher Copyright:
© The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2022.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - Arteriovenous malformations (AVMs) are complex vascular lesions characterized by abnormal connections between arteries and veins forming a tangle of vessels, without an intervening capillary bed. The lack of resistance arterioles in AVMs allows for high-velocity shunting across the nidus and can lead to rupture and subsequent hemorrhage, which is the most common manifestation of an AVM. These lesions can remain asymptomatic until a precipitating event such as seizure or hemorrhage occurs, making epidemiological estimates difficult. However, the reported incidence of symptomatic AVMs is around 1 per 100, 000 person/years with a prevalence of 0.018% in the adult population and 0.02% in the pediatric population. AVMs carry an annual rupture risk between 2% and 4% across all age groups, though associated high-risk features can significantly increase this risk. Each lesion is unique and must be evaluated based on its own specific characteristics. Due to their complexity, AVMs often require a multimodal treatment approach with various combinations of endovascular, microsurgical, and radiosurgical techniques in order to safely achieve a cure. It is therefore essential to understand the various indications, limitations, and key principles for each treatment modality which are summarized in this chapter.
AB - Arteriovenous malformations (AVMs) are complex vascular lesions characterized by abnormal connections between arteries and veins forming a tangle of vessels, without an intervening capillary bed. The lack of resistance arterioles in AVMs allows for high-velocity shunting across the nidus and can lead to rupture and subsequent hemorrhage, which is the most common manifestation of an AVM. These lesions can remain asymptomatic until a precipitating event such as seizure or hemorrhage occurs, making epidemiological estimates difficult. However, the reported incidence of symptomatic AVMs is around 1 per 100, 000 person/years with a prevalence of 0.018% in the adult population and 0.02% in the pediatric population. AVMs carry an annual rupture risk between 2% and 4% across all age groups, though associated high-risk features can significantly increase this risk. Each lesion is unique and must be evaluated based on its own specific characteristics. Due to their complexity, AVMs often require a multimodal treatment approach with various combinations of endovascular, microsurgical, and radiosurgical techniques in order to safely achieve a cure. It is therefore essential to understand the various indications, limitations, and key principles for each treatment modality which are summarized in this chapter.
KW - Arteriovenous malformation
KW - AVM
KW - Hemorrhage
KW - Vascular malformation
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U2 - 10.1007/978-3-030-88196-2_20
DO - 10.1007/978-3-030-88196-2_20
M3 - Chapter
AN - SCOPUS:85152829821
SN - 9783030881955
SP - 389
EP - 410
BT - Introduction to Vascular Neurosurgery
PB - Springer International Publishing
ER -