A Case of Infantile Meningioangiomatosis with a Separate Cyst.
10.3340/jkns.2009.46.3.252
- Author:
Seong Ho KIM
1
;
Soo Han YOON
;
Jang Hee KIM
Author Information
1. Department of Neurosurgery, College of Medicine, Yeungnam University, Daegu, Korea.
- Publication Type:Case Report
- Keywords:
Brain tumor;
Cyst;
Epilepsy;
Infant;
Neurofibromatosis
- MeSH:
Biopsy;
Brain;
Brain Neoplasms;
Child;
Craniotomy;
Edema;
Epilepsy;
Female;
Follow-Up Studies;
Hemorrhage;
Humans;
Infant;
Magnetic Resonance Imaging;
Neurofibromatoses;
Recurrence;
Seizures
- From:Journal of Korean Neurosurgical Society
2009;46(3):252-256
- CountryRepublic of Korea
- Language:English
-
Abstract:
Meningioangiomatosis (MA) is a rare congenital tumor that occurs mostly in 5-15 year old children. There have been only 5 cases previously reported that described the cystic nature within these tumors. We present a case of a MA accompanied by a separate macrocyst. A normally developed 2 year-old female patient presented with partial and generalized seizures. The brain computerized tomogram and magnetic resonance imaging revealed the presence of a calcified mass accompanied by a cyst in the right parietal area, surrounded by low density and high attenuation edema and hemorrhage. Upon right parietal craniotomy, a 1.6 cm x 1.2 cm x 0.5 cm sized plate-like, gray-white, slightly hard mass was seen and it was completely excised. Approximately 1 cm from the mass in the anterior lateral direction, a cyst was found and subsequent biopsy of the cyst wall revealed no tumor tissue, and therefore the cyst was not removed. Pathologic report demonstrated the meningioangiomatosis. Follow up examination 2 years later showed no recurrence of the tumor, and there was no evidence of neurological deficits. Authors suggest that cysts that arise in the surrounding tissues of tumors may not be tumor cysts, and do not require surgical removal.
