真性红细胞增多症和原发性血小板增多症在儿童,仍然是儿科医生的一个挑战。

IF 2.9 3区 医学 Q1 PEDIATRICS European Journal of Pediatrics Pub Date : 2025-02-04 DOI:10.1007/s00431-025-05993-1
Agathe Picard, Sophie Bayart, Marianna Deparis, Cécile Dumesnil De Maricourt, Sophie Haro, Anne Jourdain, Coralie Mallebranche, Fanny Rialland, Damien Luque Paz, Cedric Pastoret, Virginie Gandemer, Elie Cousin
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引用次数: 0

摘要

真性红细胞增多症(PV)和原发性血小板增多症(ET)是儿童、青少年和年轻人罕见的骨髓增生性肿瘤(MPN)。对于这些患者的管理尚无建议。将成人患者的知识转移到儿童身上是不可接受的。为了更好地了解儿科医生和成人血液学家遇到的困难,我们对法国18岁以下诊断为ET或PV的患者进行了全国实践分析。然后,我们介绍了来自一项多中心、描述性、回顾性研究的数据,包括17例诊断为18岁以下的ET或PV患者,来自法国7个血科。受访医生报告缺乏血液学领域的专业知识和理论培训来诊断和跟踪mpn患儿。来自17例患者(15例ET, 2例PV)的数据证实,在诊断时无症状患者的比例很高(41%)。“三阴性”患者的比例(59%)高于成人队列。60%的患者接受了骨髓活检,31%的病例在多学科工作人员会议上进行了讨论。76.5%的患者得到治疗,使用抗血栓和细胞减少药物的频率较高。中位随访45个月,无并发症发生。结论:医师坚持培训的必要性。只有积累对儿童mpn的描述,才能更好地管理这些疾病。考虑到儿科患者在诊断后出现并发症的比例很小,在与成人血液学家密切合作的随访中,快速治疗降压似乎是必不可少的。已知情况:•骨髓增生性肿瘤是一种罕见的慢性疾病,大多数情况下影响成人,但也很少在儿科患者中发现。对于真性红细胞增多症或原发性血小板增多症儿童的诊断、治疗管理或随访没有建议。新内容:•通过国家实践分析,了解成人血液病学家和儿科医生对骨髓增生性综合征患儿的管理和随访的看法。•描述了法国真性红细胞增多症或原发性血小板增多症儿童的“现实生活”随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Polycythemia vera and essential thrombocythemia in children, still a challenge for pediatricians.

Polycythemia vera (PV) and essential thrombocythemia (ET) are rare myeloproliferative neoplasms (MPN) in children, adolescents and young adults. No recommendations are available concerning these patients' management. Transposing to children the knowledge established in adult patients is not acceptable. For a better understanding of difficulties encountered by pediatricians and adult hematologists, we conducted a national practice analysis concerning follow-up of patients under 18 diagnosed with ET or PV, in France. Then, we present data from a multicentric, descriptive, retrospective study, including 17 patients with ET or PV, diagnosed under 18, coming from 7 hematopediatric departments in France. Interviewed physicians reported a lack of expertise and theoretical training in the hematological field to diagnose and follow children with MPNs. Data from 17 patients (15 ET, 2 PV) confirmed a high proportion of asymptomatic patients at the time of diagnosis (41%). Proportion of "triple-negative" patients (59%) was higher than in adult cohorts. 60% of patients underwent a bone marrow biopsy and 31% of cases were discussed during a multi-disciplinary staff meeting. 76.5% patients were treated, with a high frequency of antithrombotic and cytoreductive drugs. No complications were observed during the 45 months of median follow-up.

Conclusion: Physicians insisted on the need for training. Only the accumulation of descriptions of MPNs in children will lead to a better management of these diseases. Considering the small proportion of pediatric patients with complications after diagnosis, rapid therapeutic de-escalation seems essential to consider during the follow-up in a close collaboration with adult hematologists.

What is known: • Myeloproliferativ neoplams are rare and chronic deseases, most of the time affecting adults but also found in few pediatric patients. • There are no recommendations for the diagnosis, therapeutic management or follow-up of children with polycythemia vera or essential thrombocythemia.

What is new: • Find out how adult haematologists and paediatricians feel about the management and follow-up of paediatric patients with myeloproliferative syndrome through a national practice analysis. • Description of the "real life" follow-up of children with polycythemia vera or essential thrombocythemia in France.

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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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