Dellemijn P L, Vanneste J A
Department of Neurology, St Lucasziekenhuis, Amsterdam, The Netherlands.
Acta Neurol Scand. 1993 Oct;88(4):259-63. doi: 10.1111/j.1600-0404.1993.tb04232.x.
A 23-year-old woman presented with cerebellar hemorrhage from a cavernous angioma (CA). A history of spinal hemorrhage and a supratentorial calcified lesion on CT and MRI suggested cavernous angiomatosis of the CNS. Familial investigation in 20 relatives revealed 4 additional patients with symptomatic CA and one person with asymptomatic CA. In the symptomatic patients, CA had not been recognized as the cause of their neurologic symptoms prior to our investigation. The number of CA lesions in asymptomatic relatives was low. This study shows that, when a patient with cavernous angiomatosis of the CNS is encountered, systematic clinical and MRI investigations in other family members with a history or symptoms of neurologic disorder should be carried out.
一名23岁女性因海绵状血管瘤(CA)导致小脑出血。既往有脊髓出血史,CT和MRI显示幕上钙化灶,提示中枢神经系统海绵状血管瘤病。对20名亲属进行家族调查发现,另有4例有症状的CA患者和1例无症状的CA患者。在有症状的患者中,在我们调查之前,CA未被确认为其神经症状的病因。无症状亲属的CA病灶数量较少。本研究表明,当遇到中枢神经系统海绵状血管瘤病患者时,应对其他有神经疾病病史或症状的家庭成员进行系统的临床和MRI检查。