Delage R, Demers C, Cantin G, Roy J
Saint-Sacrement Hospital, Laval University, Quebec, Canada.
Obstet Gynecol. 1996 May;87(5 Pt 2):814-7.
Only a few cases of essential thrombocythemia in pregnant women have been reported, and the management of this myeloproliferative disorder during pregnancy remains uncertain. We report a successful pregnancy in a patient who had essential thrombocythemia and who was treated with interferon-alpha, and we review the literature for the outcome of similar patients.
A 32-year-old woman, gravida 4, para 3, aborta 0, presented at 18 weeks' gestation with two episodes of amaurosis fugax and an elevated platelet count of 2300 x 10(9)/L. The initiation of interferon-alpha led to a progressive fall of the platelet level, with no occurrence of thrombotic or hemorrhagic manifestations. Serial ultrasound examinations revealed normal fetal and placental development. The patient was delivered of a male infant at 37 weeks. Both child and placenta were normal on examination.
Our case and the current available data suggest that interferon-alpha may be the best therapeutic option for pregnant patients with essential thrombocythemia in whom myelosuppression is required.
仅有少数关于孕妇原发性血小板增多症的病例报道,孕期这种骨髓增殖性疾病的管理仍不明确。我们报告了1例患原发性血小板增多症且接受α干扰素治疗的患者成功妊娠的病例,并回顾了类似患者的文献资料以了解其结局。
一名32岁女性,孕4产3,0流产,孕18周时出现2次一过性黑矇发作,血小板计数升高至2300×10⁹/L。开始使用α干扰素后血小板水平逐渐下降,未出现血栓形成或出血表现。系列超声检查显示胎儿及胎盘发育正常。患者于37周分娩一男婴。检查发现婴儿及胎盘均正常。
我们的病例及现有数据表明,对于需要进行骨髓抑制的原发性血小板增多症孕妇,α干扰素可能是最佳治疗选择。