Treatment of moyamoya disease with STA-MCA anastomosis
- 1 November 1978
- journal article
- research article
- Published by Journal of Neurosurgery Publishing Group (JNSPG) in Journal of Neurosurgery
- Vol. 49 (5), 679-688
- https://doi.org/10.3171/jns.1978.49.5.0679
Abstract
✓ Moyamoya disease is a chronic occlusive cerebrovascular disease of unknown etiology for which no effective treatment has been found. The authors report the results of 23 superficial temporal-middle cerebral artery (STA-MCA) anastomoses and seven encephalomyosynangioses, performed on 13 cases with moyamoya disease and on four additional atypical cases. There were 10 children and seven adults in this study. The follow-up period ranged from 1 year and 4 months to 4 years and 1 month postoperatively; nine patients had excellent results, five good, and one fair; two patients were unchanged. The anastomotic procedure was most effective for transient ischemic attacks, reversible ischemic neurological deficits, and even minor or moderate neurological symptoms. The STA-MCA anastomosis appears to be an effective treatment for moyamoya disease.Keywords
This publication has 3 references indexed in Scilit:
- Clinical and Radioisotopic Follow-Up Study of ‘Moyamoya’Pediatric Neurosurgery, 1976
- An Attempt to Treat Cerebrovascular ‘Moyamoya’ Disease in ChildrenPediatric Neurosurgery, 1975
- Operative Revaskularisation des zirkulatorisch geschädigten Gehirns durch Auflage gestielter Muskellappen (Encephalo-Myo-Synangiose)Langenbecks Archives Of Surgery, 1950