原发性血小板增多症:一种罕见的疾病

Parimi Shashank, Intikabur Rahman
{"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}
引用次数: 0

摘要

原发性血小板增多症是一种病因不明的慢性骨髓增殖性疾病,其特征是持续的巨核细胞增殖,导致循环中的血小板明显增加。我们报告一位40岁的女性患者,她的主诉是过度疲劳,手指尖很少有刺痛感,全身疼痛,最初被检测到有1,775,000/mm3的极端血小板增多。在进一步的评估中,她被诊断为原发性血小板增多症,在整个随访期间没有任何进一步恶化的报告,并继续服用低剂量阿司匹林。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Essential thrombocytosis: A rare entity
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.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信