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有助于预测特发性血小板减少性紫癜诊断的初始实验室检查结果。

Initial laboratory findings useful for predicting the diagnosis of idiopathic thrombocytopenic purpura.

作者信息

Kuwana Masataka, Okazaki Yuka, Satoh Takashi, Asahi Atsuko, Kajihara Mikio, Ikeda Yasuo

机构信息

Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.

出版信息

Am J Med. 2005 Sep;118(9):1026-33. doi: 10.1016/j.amjmed.2004.12.027.

Abstract

PURPOSE

To identify initial laboratory findings useful for the later diagnosis of idiopathic thrombocytopenic purpura (ITP) in adult patients with thrombocytopenia.

SUBJECTS AND METHODS

We studied 62 consecutive adult patients who had thrombocytopenia and whose peripheral blood film was normal except for thrombocytopenia at presentation. Each patient underwent physical examination and routine laboratory tests and was prospectively followed for 22.5 +/- 9.8 months (range, 8 to 41 months). The frequency of antiglycoprotein (GP) IIb/IIIa antibody-producing B cells, the presence of platelet-associated and plasma anti-GPIIb/IIIa antibodies, the percentage of reticulated platelets, and the plasma thrombopoietin level were examined at the first visit. The final diagnosis was based on the clinical history, physical examination, complete blood test, bone marrow findings, and the clinical course at last observation.

RESULTS

Forty-six patients were diagnosed as having ITP and 16 as having another disorder, including myelodysplastic syndrome, aplastic anemia, amegakaryocytic thrombocytopenia, and reduced platelet production, with or without other cytopenias, and without dysplasia or evidence for destruction. Six initial laboratory findings discriminated ITP from other diagnoses: the absence of anemia, absence of leukocytopenia, increased frequency of anti-GPIIb/IIIa antibody-producing B cells, increased platelet-associated anti-GPIIb/IIIa antibodies, elevated percentage of reticulated platelets, and a normal or slightly increased plasma thrombopoietin level. Three or more of these ITP-associated findings were found at presentation in 44 patients (96%) with thrombocytopenia later diagnosed as ITP, compared with only 1 patient (6%) whose disorder was non-ITP.

CONCLUSION

Initial laboratory findings can well predict future diagnosis of ITP. Further studies prospectively evaluating these same diagnostic criteria on another, independent set of patients are necessary.

摘要

目的

确定有助于成年血小板减少症患者后续诊断特发性血小板减少性紫癜(ITP)的初始实验室检查结果。

对象与方法

我们研究了62例连续的成年血小板减少症患者,其外周血涂片在初诊时除血小板减少外均正常。每位患者均接受了体格检查和常规实验室检查,并进行了为期22.5±9.8个月(范围8至41个月)的前瞻性随访。在首次就诊时检测了抗糖蛋白(GP)IIb/IIIa抗体产生B细胞的频率、血小板相关和血浆抗GPIIb/IIIa抗体的存在情况、网织血小板百分比以及血浆血小板生成素水平。最终诊断基于临床病史、体格检查、全血细胞计数、骨髓检查结果以及最后一次观察时的临床病程。

结果

46例患者被诊断为ITP,16例被诊断为其他疾病,包括骨髓增生异常综合征、再生障碍性贫血、无巨核细胞性血小板减少症以及血小板生成减少,伴有或不伴有其他血细胞减少,且无发育异常或破坏证据。六项初始实验室检查结果可将ITP与其他诊断区分开来:无贫血、无白细胞减少、抗GPIIb/IIIa抗体产生B细胞频率增加、血小板相关抗GPIIb/IIIa抗体增加、网织血小板百分比升高以及血浆血小板生成素水平正常或略有升高。44例(96%)初诊时血小板减少且后来诊断为ITP的患者出现了三项或更多这些与ITP相关的检查结果,相比之下,只有1例(6%)非ITP疾病患者出现了这些结果。

结论

初始实验室检查结果可以很好地预测ITP的未来诊断。有必要对另一组独立患者前瞻性地评估这些相同诊断标准的进一步研究。

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