Sarwar M
Rev Interam Radiol. 1977 Jul;2(3):159-61.
Of the venous abnormalities in the Sturge-Weber syndrome, deep venous occlusion is an uncommon finding. As far as can be determined it has been described in only two previously recorded cases. Another such case is presented to illustrate the usefulness of this finding, in conjunction with other venous anomalies, in the diagnosis of the Sturge-Weber syndrome, especially before two years of age when calcifications in the brain may not have appeared.
在斯特奇-韦伯综合征的静脉异常中,深部静脉闭塞是一种罕见的表现。据目前所能确定,此前仅有两例相关记录。本文报告另一例这样的病例,以说明这一表现与其他静脉异常一起,在斯特奇-韦伯综合征诊断中的作用,特别是在两岁之前,此时脑部钙化可能尚未出现。