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继发性血小板增多症。

Secondary thrombocytosis.

作者信息

Vora A J, Lilleyman J S

机构信息

Department of Paediatrics, University of Sheffield.

出版信息

Arch Dis Child. 1993 Jan;68(1):88-90. doi: 10.1136/adc.68.1.88.

Abstract

To estimate the incidence and causes of secondary thrombocytosis in children, a 12 month study of all patients attending a children's hospital and discovered to have a platelet count over two times the upper normal limit (> 800 x 10(9)/l) was undertaken. Data so obtained were analysed both separately and together with those from two previous studies to gain as broad a perspective as possible. Of 7916 children who had platelet counts during the study period, 36 (0.5%) produced a value > 800 x 10(9)/l; there were 19 boys and 17 girls. There was a preponderance of young infants (median age 13 months). Twenty seven of the 36 had some sort of associated infection, bacterial in 18 and viral in nine. The other nine were either recovering from anti-neoplastic chemotherapy (n = 6), were post-operative (n = 2), or simply iron deficient (n = 1). Combining these patients with those described in previous studies allowed a review of 139 unselected children with very high platelet counts. Fifty three (38%) had infections, 29 (20%) had traumatic or surgical tissue damage, 16 (11%) had malignant disease undergoing chemotherapy or surgery, and 13 (9%) had connective tissue or autoimmune disorders. Secondary thrombocytosis is not rare and is most frequently seen in very young infants after infection. It can arise in a wide variety of other circumstances including rebound from myelosuppression, iron lack, or as part of an acute phase response. It is clinically unimportant in terms of morbidity and requires no treatment other than that for the primary condition.

摘要

为了评估儿童继发性血小板增多症的发病率及病因,我们对一家儿童医院所有血小板计数超过正常上限两倍(> 800×10⁹/L)的患儿进行了为期12个月的研究。将所获数据单独分析,并与之前两项研究的数据合并分析,以尽可能全面地了解情况。在研究期间接受血小板计数检测的7916名儿童中,36名(0.5%)血小板计数> 800×10⁹/L;其中19名男孩,17名女孩。以幼儿居多(中位年龄13个月)。36名患儿中有27名伴有某种感染,18名是细菌感染,9名是病毒感染。另外9名患儿中,6名正在从抗肿瘤化疗中恢复,2名是术后患儿,1名只是缺铁。将这些患儿与之前研究中描述的患儿合并,共纳入139名未经过筛选、血小板计数极高的儿童。其中53名(38%)有感染,29名(20%)有创伤或手术导致的组织损伤,16名(11%)有正在接受化疗或手术的恶性疾病,13名(9%)有结缔组织或自身免疫性疾病。继发性血小板增多症并不罕见,最常见于感染后的幼儿。它也可在多种其他情况下出现,包括骨髓抑制后的反弹、缺铁,或作为急性期反应的一部分。就发病率而言,它在临床上并不重要,除针对原发疾病进行治疗外无需特殊处理。

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