[儿童继发于无症状SARS-CoV2的难治性急性免疫性血小板减少性紫癜]。

Q3 Medicine
Revue medicale de Liege Pub Date : 2023-07-01
Ambre Dethier, Sophie Gatineau-Sailliant, Claire Geurten, Marie-Françoise Dresse
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引用次数: 0

摘要

急性免疫性血小板减少性紫癜(ITP)是一种罕见的COVID-19儿童并发症。严重出血可能发生,但很少危及生命。治疗是基于出血症状的严重程度和血小板减少的程度。我们报告一名7岁女童继发于COVID-19感染的严重急性ITP病例,无任何呼吸道症状。最初的临床检查显示一个大的凸起的中背血肿,紫癜性病变和咽后出血。患者在儿科重症监护病房接受监测。最初的医疗管理包括静脉注射免疫球蛋白和全身类固醇。尽管如此,出血和血小板减少恶化,继发性肉眼血尿发生,需要6小时血小板输注和增加类固醇剂量以获得充分止血。本病例是一种罕见且严重的急性小儿ITP,继发于无症状的SARS-COV2,初始治疗难治性,并开启了对二线治疗干预措施的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Pediatric refractory acute immune thrombocytopenic purpura secondary to asymptomatic SARS-CoV2].

Acute immune thrombocytopenic purpura (ITP) has been revealed as an uncommon complication of COVID-19 in children. Severe bleeding may occur but is rarely life threatening. Management is based on the severity of bleeding symptoms and the degree of thrombocytopenia. We report the case of a 7-year-old girl with severe acute ITP secondary to a COVID-19 infection -without any respiratory symptoms. The initial clinical examination showed a large bulging mediodorsal hematoma, purpuric lesions, and posterior pharyngeal hemorrhage. The patient was monitored in a pediatric intensive care unit. Initial medical management consisted of intravenous immunoglobulins and systemic steroids. Despite this treatment, bleeding and thrombocytopenia worsened, and secondary macroscopic haematuria occurred, requiring 6-hourly platelet transfusions and increased steroid doses to obtain sufficient hemostasis. This case presents a rare and severe acute pediatric ITP secondary to asymptomatic SARS-COV2 which was refractory to initial management and opens the discussion to second line therapeutic interventions.

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来源期刊
Revue medicale de Liege
Revue medicale de Liege Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
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0
期刊介绍: The Medical Review of Liege is a tool for continuous medical training being addressed to students, general practitioners, and specialists
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