{"title":"神经母细胞瘤的外科治疗。","authors":"E M Kiely","doi":"10.1007/978-3-642-72643-9_11","DOIUrl":null,"url":null,"abstract":"<p><p>Over a 33-month period, 31 infants and children had surgery for neuroblastoma. Twenty-three of the total had stage IV disease at the time of presentation and all but five had an abdominal primary tumour. In only two children was the tumour considered unresectable. The operative mortality was 3%. Neither ultrasound nor CT scanning could accurately predict resectability.</p>","PeriodicalId":76378,"journal":{"name":"Progress in pediatric surgery","volume":"22 ","pages":"140-5"},"PeriodicalIF":0.0000,"publicationDate":"1989-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"14","resultStr":"{\"title\":\"Surgery for neuroblastoma.\",\"authors\":\"E M Kiely\",\"doi\":\"10.1007/978-3-642-72643-9_11\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Over a 33-month period, 31 infants and children had surgery for neuroblastoma. Twenty-three of the total had stage IV disease at the time of presentation and all but five had an abdominal primary tumour. In only two children was the tumour considered unresectable. The operative mortality was 3%. Neither ultrasound nor CT scanning could accurately predict resectability.</p>\",\"PeriodicalId\":76378,\"journal\":{\"name\":\"Progress in pediatric surgery\",\"volume\":\"22 \",\"pages\":\"140-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"14\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Progress in pediatric surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/978-3-642-72643-9_11\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in pediatric surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/978-3-642-72643-9_11","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Over a 33-month period, 31 infants and children had surgery for neuroblastoma. Twenty-three of the total had stage IV disease at the time of presentation and all but five had an abdominal primary tumour. In only two children was the tumour considered unresectable. The operative mortality was 3%. Neither ultrasound nor CT scanning could accurately predict resectability.
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