{"title":"-地中海贫血和非霍奇金淋巴瘤","authors":"P. Patir, N. Soyer, G. Saydam","doi":"10.4172/2155-9864.1000352","DOIUrl":null,"url":null,"abstract":"Beta-thalassemia is a frequent genetic disorder in the Mediterranean area, presenting deficLt of beta-globin chain synthesis, reduced hemoglobin in red blood cells. AÂe occurence of lymphoma in thalassemia has rarely been reported. We hereby report a case of thalessemia major developing non-Hodgkin lymphoma.","PeriodicalId":182392,"journal":{"name":"Journal of Blood Disorders and Transfusion","volume":"23 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Beta-thalassemia Major and Non-Hodgkin Lymphoma\",\"authors\":\"P. Patir, N. Soyer, G. Saydam\",\"doi\":\"10.4172/2155-9864.1000352\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Beta-thalassemia is a frequent genetic disorder in the Mediterranean area, presenting deficLt of beta-globin chain synthesis, reduced hemoglobin in red blood cells. AÂe occurence of lymphoma in thalassemia has rarely been reported. We hereby report a case of thalessemia major developing non-Hodgkin lymphoma.\",\"PeriodicalId\":182392,\"journal\":{\"name\":\"Journal of Blood Disorders and Transfusion\",\"volume\":\"23 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-05-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Blood Disorders and Transfusion\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2155-9864.1000352\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Blood Disorders and Transfusion","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2155-9864.1000352","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Beta-thalassemia is a frequent genetic disorder in the Mediterranean area, presenting deficLt of beta-globin chain synthesis, reduced hemoglobin in red blood cells. AÂe occurence of lymphoma in thalassemia has rarely been reported. We hereby report a case of thalessemia major developing non-Hodgkin lymphoma.