原发性血小板增多症并发多发性骨髓瘤。

Clinical and laboratory haematology Pub Date : 1995-12-01
P R Kelsey, K Patel
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引用次数: 0

摘要

我们描述了一个患有原发性血小板血症的患者,他在原发性血小板血症的初步诊断7年后发展为多发性骨髓瘤。一名50岁白人女性于1987年以腰痛、脚踝疼痛肿胀和足部灼烧2年病史就诊。她的实验室检查显示诊断为原发性血小板血症。最初,她用布硫芬治疗了6个月,但收效甚微。随后,她接受羟基脲治疗,症状明显缓解,血小板计数减少。7年后,她出现骨痛和贫血,实验室检查证实多发性骨髓瘤的诊断。
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Essential thrombocythaemia followed by multiple myeloma in the same patient.

We describe a patient with essential thrombocythaemia who developed multiple myeloma 7 years after an initial diagnosis of essential thrombocythaemia. A 50-year-old white female presented in 1987 with a 2 year history of low backache, painful swollen ankles and burning feet. Her laboratory investigations suggested a diagnosis of essential thrombocythaemia. Initially she was treated with busulphan without much benefit for 6 months. Subsequently she was treated with hydroxyurea with significant relief of her symptoms and reduction in her platelet count. Seven years after her initial presentation she developed bone pains and anaemia with laboratory investigations confirming a diagnosis of multiple myeloma.

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Reply to Cavill Reference values for the activated partial thromboplastin time in infants using a synthetic reagent. A case of idiopathic hypereosinophilic syndrome with hypersegmented and hypogranular eosinophils. Reference intervals for haematological parameters in urban school children and adolescents. Atlas of Blood Cell Differentiation (Interactive CD‐ROM)
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