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极高的血小板计数率表明先天性膈疝患者骨髓活性增高和脾脏功能障碍。

High rate of extreme thrombocytosis indicates bone marrow hyperactivity and splenic dysfunction among congenital diaphragmatic hernia patients.

机构信息

Division of Neonatology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Department of General Surgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

出版信息

Platelets. 2022 Jul 4;33(5):787-789. doi: 10.1080/09537104.2021.1994546. Epub 2021 Oct 26.

Abstract

Pediatric extreme thrombocytosis (EXT, platelet count > 1000 x 10/µL) is rare. In a single center retrospective analysis of hospitalized children with EXT, infants with congenital diaphragmatic hernia (CDH) were overrepresented. In general pediatric patients, EXT is usually secondary to infection or inflammation, but most of the 14 CDH patients with EXT had no identifiable inciting factor. Instead, there was evidence that splenic dysfunction and bone marrow hyperactivity underlied EXT in CDH patients. None were associated with bleeding or thrombosis. Our findings identify mechanisms underlying EXT, and aid clinical interpretation and management of EXT in the pediatric population.

摘要

儿科特发性血小板增多症(EXT,血小板计数>1000×10/µL)较为罕见。在对住院 EXT 患儿进行的单中心回顾性分析中,患有先天性膈疝(CDH)的婴儿所占比例过高。在一般儿科患者中,EXT 通常继发于感染或炎症,但 EXT 的 14 名 CDH 患者中大多数没有明确的诱发因素。相反,有证据表明,CDH 患者的脾功能障碍和骨髓过度活跃是 EXT 的基础。无一例与出血或血栓形成有关。我们的研究结果确定了 EXT 的发病机制,并有助于对儿科人群 EXT 的临床解释和管理。

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