{"title":"原发性血小板增多症:一种罕见的疾病","authors":"Parimi Shashank, Intikabur Rahman","doi":"10.4103/ajoim.ajoim_25_22","DOIUrl":null,"url":null,"abstract":"Essential thrombocytosis is a chronic myeloproliferative disorder of unknown etiology, which is characterized by persistent megakaryocytic proliferation, resulting in markedly increased platelets in circulation. We present the case of a 40-year-old female patient, who came with complaints of excessive tiredness, infrequent tingling sensation at the tip of her fingers, and generalized body ache, and was initially detected to have extreme thrombocytosis of 1,775,000/mm3. On further evaluation, she was diagnosed with essential thrombocytosis and did not report any further deterioration throughout the follow-up period and is being maintained on low-dose aspirin.","PeriodicalId":426816,"journal":{"name":"Assam Journal of Internal Medicine","volume":"140 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Essential thrombocytosis: A rare entity\",\"authors\":\"Parimi Shashank, Intikabur Rahman\",\"doi\":\"10.4103/ajoim.ajoim_25_22\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Essential thrombocytosis is a chronic myeloproliferative disorder of unknown etiology, which is characterized by persistent megakaryocytic proliferation, resulting in markedly increased platelets in circulation. We present the case of a 40-year-old female patient, who came with complaints of excessive tiredness, infrequent tingling sensation at the tip of her fingers, and generalized body ache, and was initially detected to have extreme thrombocytosis of 1,775,000/mm3. On further evaluation, she was diagnosed with essential thrombocytosis and did not report any further deterioration throughout the follow-up period and is being maintained on low-dose aspirin.\",\"PeriodicalId\":426816,\"journal\":{\"name\":\"Assam Journal of Internal Medicine\",\"volume\":\"140 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Assam Journal of Internal Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/ajoim.ajoim_25_22\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Assam Journal of Internal Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ajoim.ajoim_25_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Essential thrombocytosis is a chronic myeloproliferative disorder of unknown etiology, which is characterized by persistent megakaryocytic proliferation, resulting in markedly increased platelets in circulation. We present the case of a 40-year-old female patient, who came with complaints of excessive tiredness, infrequent tingling sensation at the tip of her fingers, and generalized body ache, and was initially detected to have extreme thrombocytosis of 1,775,000/mm3. On further evaluation, she was diagnosed with essential thrombocytosis and did not report any further deterioration throughout the follow-up period and is being maintained on low-dose aspirin.