Hiroaki Matsumoto1, Kanehisa Kohno. 1. Department of Neurosurgery, Ehime Prefectural Central Hospital, Matsuyama-shi, Ehime, Japan. hiroaki-matsu@umin.ac.jp
Abstract
BACKGROUND: Many modified surgical techniques for moyamoya disease have been developed, and each of which has some advantages and disadvantages. We report the indication for one-stage extensive indirect vascular reconstructive surgery that is our original technique for pediatric moyamoya disease. CASE DESCRIPTION: Case 1 was a 3-year-old boy who had TIAs involving the bilateral extremities and provoked by intense crying. Case 2 was a 5-year-old girl who had TIAs involving the right extremities and provoked by intense crying. Case 3 was an 8-year-old girl who had frequent TIAs involving the bilateral extremities. Case 4 was a 3-year-old boy who had mild tetraplegia due to bilateral cerebral infarction. In all cases but case 4, preoperative investigations demonstrated same-stage moyamoya disease. In case 4, preoperative investigations demonstrated different-stage moyamoya disease in which acute progression of bilateral major arterial stenosis occurred. Hence, all patients underwent one-stage extensive indirect vascular reconstructive surgery of the bilateral cerebral hemispheres. Postoperative investigations revealed the development of rich neovascularization, disappearance of clinical symptoms in all cases. CONCLUSIONS: We recommend one-stage extensive indirect vascular reconstructive surgery for pediatric moyamoya disease, particularly for patients younger than 5 years, when preoperative investigations reveal a same-stage case or bilateral acute progressive case.
BACKGROUND: Many modified surgical techniques for moyamoya disease have been developed, and each of which has some advantages and disadvantages. We report the indication for one-stage extensive indirect vascular reconstructive surgery that is our original technique for pediatric moyamoya disease. CASE DESCRIPTION: Case 1 was a 3-year-old boy who had TIAs involving the bilateral extremities and provoked by intense crying. Case 2 was a 5-year-old girl who had TIAs involving the right extremities and provoked by intense crying. Case 3 was an 8-year-old girl who had frequent TIAs involving the bilateral extremities. Case 4 was a 3-year-old boy who had mild tetraplegia due to bilateral cerebral infarction. In all cases but case 4, preoperative investigations demonstrated same-stage moyamoya disease. In case 4, preoperative investigations demonstrated different-stage moyamoya disease in which acute progression of bilateral major arterial stenosis occurred. Hence, all patients underwent one-stage extensive indirect vascular reconstructive surgery of the bilateral cerebral hemispheres. Postoperative investigations revealed the development of rich neovascularization, disappearance of clinical symptoms in all cases. CONCLUSIONS: We recommend one-stage extensive indirect vascular reconstructive surgery for pediatric moyamoya disease, particularly for patients younger than 5 years, when preoperative investigations reveal a same-stage case or bilateral acute progressive case.