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妊娠合并费城染色体阴性骨髓增殖性肿瘤的管理。

How we manage Philadelphia-negative myeloproliferative neoplasms in pregnancy.

机构信息

Haematology Department, Guys and St. Thomas' NHS Foundation Trust, London, UK.

出版信息

Br J Haematol. 2020 May;189(4):625-634. doi: 10.1111/bjh.16453. Epub 2020 Mar 9.

Abstract

The combined incidence of classical Philadelphia-negative myeloproliferative neoplasm (MPN) is 6-9/100 000 with a peak frequency between 50 and 70 years. MPN is less frequent in women of reproductive age. However, for essential thrombocythaemia (ET) in particular there is a second peak in women of reproductive age and 15% of polycythaemia vera (PV) patients are less than 40 years of age at the time of diagnosis. Thus these diseases are encountered in women of reproductive potential and may be diagnosed in pregnancy or in women being investigated for recurrent pregnancy loss. The incidence of MPN pregnancies is 3·2/100 000 maternities per year in the UK. The majority of data regarding Philadelphia-negative MPNs relates to patients with ET, for which the literature suggests significant maternal morbidity and poor fetal outcome; specifically maternal thrombosis and haemorrhage, miscarriage, pre-eclampsia, intrauterine growth restriction (IUGR), stillbirth and premature delivery as summarised in the recent systematic review and meta-analysis in Blood, 2018, 132, 3046. The literature for PV is more sparse but increasing and is concordant with ET pregnancy outcomes. The literature regarding primary myelofibrosis (PMF) is even more scarce. Treatment options include aspirin, venesection, low molecular weight heparin (LMWH) and cytoreductive therapy. Data and management recommendations are often extrapolated from other pro-thrombotic conditions or from ET to PV and PMF. Women of reproductive age with a diagnosis of MPN should receive information and assurance regarding management and outcome of future pregnancies. From pre-conceptual planning to the post-partum period, women should have access to joint care from an obstetrician with experience of high-risk pregnancies and a haematologist in a multidisciplinary setting. This paper provides an update with regards to Philadelphia-negative MPN in pregnancy, details local practise in an internationally recognised centre for patients with MPN and outlines a future research strategy.

摘要

经典费城阴性骨髓增殖性肿瘤(MPN)的合并发病率为每 10 万人中有 6-9 人,发病高峰在 50-70 岁之间。MPN 在育龄期女性中较少见。然而,尤其是特发性血小板增多症(ET),在育龄期女性中存在第二个发病高峰,15%的真性红细胞增多症(PV)患者在诊断时年龄小于 40 岁。因此,这些疾病在有生育能力的女性中会被遇到,并且可能在怀孕期间或因反复妊娠丢失而被诊断出来。在英国,MPN 妊娠的发病率为每年每 10 万例产妇中 3.2 例。关于费城阴性 MPN 的大多数数据都与 ET 患者有关,文献表明 ET 患者有明显的母体发病率和不良的胎儿结局;具体表现为母体血栓形成和出血、流产、先兆子痫、胎儿宫内生长受限(IUGR)、死产和早产,这在 2018 年发表于《Blood》的系统评价和荟萃分析中有所总结。PV 的文献更为稀少但在增加,并且与 ET 妊娠结局一致。PMF 的文献则更加稀少。治疗选择包括阿司匹林、放血、低分子肝素(LMWH)和细胞减少性治疗。数据和管理建议通常从其他血栓形成倾向的疾病或从 ET 到 PV 和 PMF 中推断出来。诊断为 MPN 的育龄期女性应获得关于未来妊娠管理和结局的信息和保证。从孕前计划到产后期间,女性应该能够在多学科环境中获得有高危妊娠经验的产科医生和血液科医生的联合护理。本文就妊娠期间费城阴性 MPN 提供了最新信息,详细介绍了国际公认的 MPN 中心的当地实践,并概述了未来的研究策略。

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