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年轻患者的真性红细胞增多症和原发性血小板增多症。

Polycythemia vera and essential thrombocythemia in young patients.

作者信息

Frezzato M, Ruggeri M, Castaman G, Rodeghiero F

机构信息

Department of Hematology, San Bortolo Hospital, Vicenza, Italy.

出版信息

Haematologica. 1993 Nov-Dec;78(6 Suppl 2):11-7.

PMID:8039752
Abstract

BACKGROUND AND METHODS

Polycythemia vera (PV) and essential thrombocythemia (ET) in young patients are rarely reported. Their natural histories seem to differ from those of older patients and the best treatment is still uncertain. In this follow-up study we have evaluated a cohort of 64 consecutive patients younger than 40 to determine the incidence of thrombohemorrhagic events and the long-term outcome.

RESULTS

Twenty-eight patients (20 M; 8 F) had PV, and 36 ET (21 F, 15 M). Mean follow-up was 8.2 years (range 4 months-16.7 years) in PV and 6.5 years (range 5 months-15 years) in ET. Thrombohemorrhagic symptoms were present at diagnosis in 10/28 patients (35%) with PV and in 12/36 patients (33%) with ET; during follow-up in 15/28 PV patients (53%) and in 13/36 ET patients (36%). Thrombotic events were the most frequent symptoms, both at diagnosis (52% in PV, 65% in ET) and during follow-up (43% in PV, 52% in ET). A total of 19/28 PV patients (67%) and 17/36 ET patients (47%) had thrombotic complications. Hemorrhagic complications at diagnosis were 4% and during follow-up 13% in PV, and 15% and 13% in ET. A total of 5/28 (18%) PV and 6/36 (17%) ET patients had hemorrhagic events. No laboratory parameter, including platelet count, was predictive of these events. Five PV patients had major thrombotic complications (18%). Four PV patients died (14%), 2 because of ANLL (7%), 2 because of thrombotic events (7%). Four ET patients experienced major complications, in three cases thrombotic (8.3%), in one hemorrhagic. No leukemic transformation occurred in ET and no ET patient died.

CONCLUSIONS

In our experience, severe thrombohemorrhagic complications are present in young patients with PV and ET, which excludes young age as a favorable prognostic factor. Treatment also seems advisable for young patients and myelosuppressive treatment might be required. Prospective studies are urgently needed to assess the best treatment for this particular subset of patients.

摘要

背景与方法

年轻患者的真性红细胞增多症(PV)和原发性血小板增多症(ET)鲜有报道。它们的自然病史似乎与老年患者不同,最佳治疗方法仍不明确。在这项随访研究中,我们评估了64例年龄小于40岁的连续患者队列,以确定血栓出血事件的发生率和长期预后。

结果

28例患者(20例男性;8例女性)患有PV,36例患有ET(21例女性,15例男性)。PV患者的平均随访时间为8.2年(范围4个月至16.7年),ET患者为6.5年(范围5个月至15年)。10/28例(35%)PV患者和12/36例(33%)ET患者在诊断时有血栓出血症状;随访期间,15/28例PV患者(53%)和13/36例ET患者(36%)出现该症状。血栓形成事件是最常见的症状,在诊断时(PV患者中为52%,ET患者中为65%)和随访期间(PV患者中为43%,ET患者中为52%)均如此。共有19/28例PV患者(67%)和17/36例ET患者(47%)发生血栓并发症。PV患者诊断时出血并发症为4%,随访期间为13%,ET患者分别为15%和13%。共有5/28例(18%)PV患者和6/36例(17%)ET患者发生出血事件。包括血小板计数在内,没有实验室参数可预测这些事件。5例PV患者发生严重血栓并发症(18%)。4例PV患者死亡(14%),2例因急性非淋巴细胞白血病(ANLL)(7%),2例因血栓形成事件(7%)。4例ET患者出现严重并发症,3例为血栓形成(8.3%),1例为出血。ET患者未发生白血病转化,也无ET患者死亡。

结论

根据我们的经验,年轻的PV和ET患者存在严重的血栓出血并发症,这排除了年轻是一个有利的预后因素。对年轻患者进行治疗似乎也是可取的,可能需要进行骨髓抑制治疗。迫切需要进行前瞻性研究,以评估针对这一特定患者亚组的最佳治疗方法。

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