Publication | Closed Access
Spontaneous Carotid-Cavernous Fistula
97
Citations
7
References
1965
Year
Ehlers-danlos SyndromeSpontaneous Carotid-cavernous FistulaMedicineSurgical PathologyHistopathologyVascular MalformationVascular SurgeryPathologyPleural EffusionCollagen TissueAngiologyProtean ManifestationsNeurovascular DiseaseConnective Tissue Disease
THE PROTEAN manifestations of Ehlers-Danlos syndrome, a rare disease of congenital nature involving body structures of mesodermal origin, are well known. Considered as a disturbance of the connective tissue, the abnormality concerns mainly the elastic and more particularly the collagen tissue throughout the body. This disorder is characterized by hyperelasticity of the skin, hyperextensibility of the joints, and histories of "easy bruising" with cutaneous hemorrhage and prolonged poorly controlled bleeding with surgical procedures. More dramatic manifestations of the disorder in other organ systems occur, eg, spontaneous rupture of the heart and lung, ectasia of the viscera, cardiac anomalies, diaphragmatic hernia, and gastrointestinal diverticula. Recently, Rubenstein and Cohen<sup>13</sup>described as unique a patient with Ehlers-Danlos syndrome associated with multiple intracranial aneurysms and spontaneous subarachnoid hemorrhage. Aneurysm of the larger vessels (aorta) has been recorded by McKusick<sup>12</sup>in this syndrome. There appears to be only one reference in the
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