原发性血小板增多症:一种罕见的疾病

Parimi Shashank, Intikabur Rahman
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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。
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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.
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