A Case Of Cerebellar Hemorrhage Associated with Cavernous Hemangioma and Developmental Venous Anomaly.
- Author:
Ji Yon LEE
;
Sung Hwan KIM
;
Soo Han YOON
- Publication Type:Original Article
- MeSH:
Cerebellar Diseases;
Cerebral Angiography;
Child, Preschool;
Drainage;
Endothelial Cells;
Female;
Gait;
Headache;
Hemangioma, Cavernous*;
Hematoma;
Hemorrhage*;
Humans;
Intracranial Hemorrhages;
Magnetic Resonance Imaging;
Neurologic Manifestations;
Seizures;
Vascular Malformations;
Vomiting
- From:
Journal of the Korean Child Neurology Society
1998;5(2):361-366
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Developmental venous anomalies are congenital anomalies of the intracranial venous drainage and clinically asymptomatic. Cavernous hemangiomas are vascular malformations composed of dilated vascular channels lined with a single layer of endothelial cells without any intervening normal neural tissue. Although, cavernous hemangioma may be clinically silent, but frequently cause variable neurologic manifestations; intracranial hemorrhage, seizures, and focal neurologic deficits. Frequent association of these two diseases has already been reported and it has been suggested that cavernous hemangiomas not the developmental venous anomalies that cause the acute clinical symptoms. A 4 year old girl with sudden onset of headache, vomiting, gait disturbance and signs of unilateral cerebellar dysfunction 2 days before admission showed a 2.5x2.5cm sized hematoma with heterogenous signal intensity both in CT and MRI in the left cerebellar hemisphere. Four-vessel cerebral angiography revealed characteristic findings of developmental venous anomalies. Pathologic findings of the surgically removed hematoma disclosed typical feature of cavernous hemangioma. Based on the findings in this case and review of the literatures, we concluded that the possibility of other diseases such as cavernous hemangiomas must be considered in patients who has intracranial hemorrhage due to the developmental venous anomalies.
