Spontaneous Dissection of Three Major Coronary Arteries Subsequent to Cystic Medial Necrosis

CHEST Journal ◽  
1999 ◽  
Vol 116 (5) ◽  
pp. 1473-1475 ◽  
Author(s):  
Viviane M. Conraads ◽  
Anne Vorlat ◽  
Cecile G. Colpaert ◽  
Inez E. Rodrigus ◽  
Rudi J. De Paep ◽  
...  
Author(s):  
John H.N. Deck

ABSTRACT:Spontaneous dissection of a major subarachnoid artery is an uncommon cause of stroke in young and apparently healthy individuals. Such dissection does not correlate well with systemic conditions such as emboli, thrombotic or hemorrhagic tendencies or hypertension, nor with disease of blood vessels such as atherosclerosis, fibromuscular dysplasia, cystic medial necrosis or Moya-Moya disease. Unusual exertion has been implicated as a factor in some cases. Gap defects were found in the internal elastic lamina near the site of dissection in three of four cases of spontaneous dissection reported here. It is suggested that such defects, because of their unusual size or number, may be responsible for initiating dissection in susceptible individuals. A detailed study of the major cerebral arteries in cases of dissection and control cases to document the size and frequency of such defects could shed light on the pathogenesis of spontaneous dissection. The subsequent course of events tends to differ in the internal carotid and vertebro-basilar systems. In most cases, the dissection in the internal carotid system is sub-intimal leading to thrombosis and cerebral infarction, while in the vertebrobasilar system dissection lies between the media and adventitia leading to subarachnoid hemorrhage. It is not known what structural differences of the two arterial systems may underlie this difference in the pattern of arterial dissection.


VASA ◽  
2011 ◽  
Vol 40 (4) ◽  
pp. 336-337
Author(s):  
Leu ◽  
Gary ◽  
Brodmann

1998 ◽  
Vol 36 (2) ◽  
pp. 113-118
Author(s):  
C. Farina ◽  
A. Gamba ◽  
R. Tambini ◽  
H. Beguin ◽  
J.L. Trouillet

1990 ◽  
Vol 49 (3) ◽  
pp. 301
Author(s):  
D. P. Fosmire ◽  
L. Pitts ◽  
C. Jacques ◽  
C. M. Greco

ESC CardioMed ◽  
2018 ◽  
pp. 2613-2615
Author(s):  
Folkert Meijboom ◽  
Gert-Jan Sieswerda

There is a genetic cause of bicuspid aortic valve. Dilatation of the aortic root and ascending aorta has long been considered genetically determined too and treated accordingly. In recent years, basic research combined with advanced cardiac imaging has made a strong case for another cause of this dilatation: an altered flow profile in the ascending aorta due to the abnormal geometry of the bicuspid valve, leading to an area of altered wall shear stress, which in turn leads to remodelling of the aortic wall, with apoptosis of vascular smooth muscle cells and disruption of media layer as a result. These histological changes, previously referred to as cystic medial necrosis, form the basis of a loss of structural integrity of the aortic wall, which makes it prone to dilatation, dissection, and rupture.


2007 ◽  
Vol 83 (2) ◽  
pp. 668-670 ◽  
Author(s):  
Koji Takeda ◽  
Goro Matsumiya ◽  
Motonobu Nishimura ◽  
Hajime Matsue ◽  
Yasuhiko Tomita ◽  
...  

1974 ◽  
Vol 109 (1) ◽  
pp. 84 ◽  
Author(s):  
Arthur J. Roberts

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