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原发性混合型冷球蛋白血症(II型)一例中的假性血小板增多症和假性白细胞增多症

Pseudothrombocytosis and pseudoleukocytosis in a case of essential mixed cryoglobulinemia (type II).

作者信息

Di Giovanni S, De Matteis M A, Ciocca D, Cirella M P, Nanni Costa M P

出版信息

Clin Exp Rheumatol. 1986 Apr-Jun;4(2):143-5.

PMID:3731571
Abstract

Pseudothrombocytosis and pseudoleukocytosis occurred in a patient with essential mixed cryoglobulinemia (EMC) and atypical cutaneous ulcers, when the blood cell counts were estimated by the Model S Plus Coulter Counter. The spurious cell counts were found in serum as well as in plasma and whole blood, so the involvement of fibrinogen in this phenomenon is questioned. When timed serial counts were performed on whole blood at room temperature the highest value of WBCs was detected one hour after sample collection and that of platelets occurred at 6 hours, when leukocytosis had disappeared. Possible explanations for this phenomenon are offered.

摘要

一名患有原发性混合性冷球蛋白血症(EMC)和非典型皮肤溃疡的患者,在用S Plus型号库尔特计数器估算血细胞计数时出现了假性血小板增多症和假性白细胞增多症。在血清、血浆和全血中均发现了假性细胞计数,因此对纤维蛋白原参与此现象提出质疑。在室温下对全血进行定时连续计数时,样本采集后1小时检测到白细胞的最高值,血小板的最高值出现在6小时,此时白细胞增多已消失。文中给出了对此现象的可能解释。

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