{"title":"骨肿瘤的流行病学。","authors":"Måns Åkerman, Henryk A Domanski, Kjell Jonsson","doi":"10.1159/000242479","DOIUrl":null,"url":null,"abstract":"As primary bone tumours are relatively uncommon, it is difficult to assemble meaningful data with regard to their relative frequency and incidence. An extensive investigation of the data on 2,627 cases collected between 1973 and 1987 from 9 geographical areas in the United States showed that primary bone sarcomas constituted only 0.2% of all malignant tumors (table 1) [2]. The incidence rate was 0.8/100,000, and showed no tendency to change during the time period under study. According to the Swedish National Cancer Registry 2004, the incidence rate per 100,000 inhabitants was 0.6 for chondrosarcoma, 0.42 for osteosarcoma and 0.29 for Ewing’s sarcoma. The relative frequencies are reported below exclude lymphohaematopoetic tumours. In the above investigation, osteosarcoma was the most frequent primary bone sarcoma, followed by chondrosarcoma, Ewing’s sarcoma and chordoma. There were only 4 cases of adamantinoma among the 2,627 cases studied. One major monograph on bone tumors [3] reviewed 4,138 malignant primary bone tumours. In this series osteosarcoma was the most frequent tumour, followed by chondrosarcoma, Ewing’s sarcoma and chordoma. Twenty-three adamantinomas were diagnosed among the cases studied. There were 2,028 benign tumours. The 5 most common benign tumours were osteochondroma, giant cell tumour, chondroma, osteid osteoma and metaphyseal fibrous defect.","PeriodicalId":18805,"journal":{"name":"Monographs in clinical cytology","volume":"19 ","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000242479","citationCount":"0","resultStr":"{\"title\":\"Epidemiology of bone tumours.\",\"authors\":\"Måns Åkerman, Henryk A Domanski, Kjell Jonsson\",\"doi\":\"10.1159/000242479\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"As primary bone tumours are relatively uncommon, it is difficult to assemble meaningful data with regard to their relative frequency and incidence. An extensive investigation of the data on 2,627 cases collected between 1973 and 1987 from 9 geographical areas in the United States showed that primary bone sarcomas constituted only 0.2% of all malignant tumors (table 1) [2]. The incidence rate was 0.8/100,000, and showed no tendency to change during the time period under study. According to the Swedish National Cancer Registry 2004, the incidence rate per 100,000 inhabitants was 0.6 for chondrosarcoma, 0.42 for osteosarcoma and 0.29 for Ewing’s sarcoma. The relative frequencies are reported below exclude lymphohaematopoetic tumours. In the above investigation, osteosarcoma was the most frequent primary bone sarcoma, followed by chondrosarcoma, Ewing’s sarcoma and chordoma. There were only 4 cases of adamantinoma among the 2,627 cases studied. One major monograph on bone tumors [3] reviewed 4,138 malignant primary bone tumours. In this series osteosarcoma was the most frequent tumour, followed by chondrosarcoma, Ewing’s sarcoma and chordoma. Twenty-three adamantinomas were diagnosed among the cases studied. There were 2,028 benign tumours. The 5 most common benign tumours were osteochondroma, giant cell tumour, chondroma, osteid osteoma and metaphyseal fibrous defect.\",\"PeriodicalId\":18805,\"journal\":{\"name\":\"Monographs in clinical cytology\",\"volume\":\"19 \",\"pages\":\"1-2\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2010-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1159/000242479\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Monographs in clinical cytology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000242479\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2009/9/23 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Monographs in clinical cytology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000242479","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2009/9/23 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
As primary bone tumours are relatively uncommon, it is difficult to assemble meaningful data with regard to their relative frequency and incidence. An extensive investigation of the data on 2,627 cases collected between 1973 and 1987 from 9 geographical areas in the United States showed that primary bone sarcomas constituted only 0.2% of all malignant tumors (table 1) [2]. The incidence rate was 0.8/100,000, and showed no tendency to change during the time period under study. According to the Swedish National Cancer Registry 2004, the incidence rate per 100,000 inhabitants was 0.6 for chondrosarcoma, 0.42 for osteosarcoma and 0.29 for Ewing’s sarcoma. The relative frequencies are reported below exclude lymphohaematopoetic tumours. In the above investigation, osteosarcoma was the most frequent primary bone sarcoma, followed by chondrosarcoma, Ewing’s sarcoma and chordoma. There were only 4 cases of adamantinoma among the 2,627 cases studied. One major monograph on bone tumors [3] reviewed 4,138 malignant primary bone tumours. In this series osteosarcoma was the most frequent tumour, followed by chondrosarcoma, Ewing’s sarcoma and chordoma. Twenty-three adamantinomas were diagnosed among the cases studied. There were 2,028 benign tumours. The 5 most common benign tumours were osteochondroma, giant cell tumour, chondroma, osteid osteoma and metaphyseal fibrous defect.
期刊介绍:
Monographs in this series have given the field of cytology an outstanding set of reference works. Volumes perform the important function of correlating extensive basic and clinical findings and applying these to discuss how innovations in cytology can improve patient diagnosis and management. Readers will find descriptions of techniques offering greater simplicity, speed, patient comfort and cost effectiveness as well as improved diagnostic precision. The immense utility of these texts has resulted in the release of updated second editions of earlier volumes, which continue to meet the popular demand for access to this material.