TY - CHAP
T1 - Cerebral cavernous malformations and developmental venous anomalies
AU - Metellus, Philippe
AU - Kharkar, Siddharth
AU - Lin, Doris
AU - Kapoor, Sumit
AU - Rigamonti, Daniele
N1 - Publisher Copyright:
© Cambridge University Press 2008 and 2009.
PY - 2008/1/1
Y1 - 2008/1/1
N2 - Cavernous malformations (CMs) are angiographically occult vascular malformation considered as congenital anomalies of the brain. The first comprehensive review by Voigt and Yasargil (1976) provided a good overview of the knowledge of CMs in the 1970s with special references to epidemiology, diagnosis, and clinical findings. Over the past two decades numerous articles on CMs have been published, and our knowledge of this pathology has considerably evolved (Awad and Robinson, 1993; Moriarity, Clatterbuck, and Rigamonti, 1999; Simard et al., 1986). There is now general agreement on the diagnosis and pathology of CMs, but controversies still persist in the recent literature concerning their natural history and dynamic nature. Recent literature concerning the genetics of CMs and their biology with special reference to angiogenesis and cellular proliferation has provided new clues to the pathogenesis and pathophysiology of these malformations.
AB - Cavernous malformations (CMs) are angiographically occult vascular malformation considered as congenital anomalies of the brain. The first comprehensive review by Voigt and Yasargil (1976) provided a good overview of the knowledge of CMs in the 1970s with special references to epidemiology, diagnosis, and clinical findings. Over the past two decades numerous articles on CMs have been published, and our knowledge of this pathology has considerably evolved (Awad and Robinson, 1993; Moriarity, Clatterbuck, and Rigamonti, 1999; Simard et al., 1986). There is now general agreement on the diagnosis and pathology of CMs, but controversies still persist in the recent literature concerning their natural history and dynamic nature. Recent literature concerning the genetics of CMs and their biology with special reference to angiogenesis and cellular proliferation has provided new clues to the pathogenesis and pathophysiology of these malformations.
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U2 - 10.1017/CBO9780511544897.030
DO - 10.1017/CBO9780511544897.030
M3 - Chapter
AN - SCOPUS:84893008967
SN - 9780521874373
SP - 189
EP - 220
BT - Uncommon Causes of Stroke, 2nd Edition
PB - Cambridge University Press
ER -