@article{oai:kanazawa-u.repo.nii.ac.jp:00027002,
 author = {Hayashi, Yasuhiko and Tohma, Yasuo and Mouri, Masanao and Yamashima, Tetsumori and Yamashita, Junkoh},
 issue = {2},
 journal = {Neurologia Medico-Chirurgica},
 month = {Jan},
 note = {A 16-year-old girl presented with multiple cerebral cavernous angiomas with calcifications due to repeated hemorrhages and a thrombosed cerebral arteriovenous malformation (AVM). Her 18-year-old elder sister also had multiple cerebral cavernous angiomas associated with calcifications, which suggested presence of repeated previous hemorrhages. Surgical removal via a right occipital craniotomy resulted in a good outcome. The histological diagnosis was thrombosed AVM. Evaluation of congenital vascular anomaly needs to take into consideration the combination of other congenital vascular anomalies and their familial occurrence., 金沢大学医薬保健研究域医学系, 金沢大学附属病院脳神経外科},
 pages = {67--72},
 title = {Congenital multiple cavernous angiomas associated with thrombosed arteriovenous malformation of the brain - Case report},
 volume = {42},
 year = {2002}
}