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Spontaneous resolution of extreme thrombocytosis in 2 children

机译:自发解决2名儿童的极端血小板增多症

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Essential thrombocytosis (ET) is rare in children, sometimes difficult to be distinguished from secondary thrombocytosis. This report concerns 2 children with extreme thrombocytosis of 4100 × 10 9/L and 1644 × 10 9/L with partial and complete remission at 3 months and 4 years from diagnosis, with a follow-up of 4 and 17 years, respectively, with no cytoreduction therapy. Diagnosis of ET was suggested according to accepted criteria. However, spontaneous remission of the thrombocytosis argues for the diagnosis of secondary thrombocytosis. These patients highlight the complexity of distinguishing childhood ET from secondary thrombocytosis and the need for cautious personalized decision on cytoreduction therapy.
机译:必需的血小板增多症(ET)在儿童中很少见,有时难以与继发性血小板增多症区分开。该报告涉及2名儿童的极端血小板增多症,分别为4100×10 9 / L和1644×10 9 / L,在确诊后3个月和4年时部分缓解和完全缓解,并分别随访4年和17岁。没有减细胞疗法。建议根据公认的标准诊断ET。然而,血小板增多症的自发缓解为继发性血小板增多症的诊​​断提供了依据。这些患者突显了区分儿童ET与继发性血小板增多症的复杂性,以及对细胞减少疗法的谨慎个性化决策的需求。

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