Extremity Findings of Methotrexate Embryopathy

The Hand Pub Date : 2020-01-01 DOI:10.1177/1558944719837657
Esperanza Mantilla-Rivas, Ashleigh Brennan, A. Goldrich, Justin R Bryant, A. Oh, G. Rogers
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引用次数: 5

Abstract

Background: Methotrexate (MTX) is widely used as an immunosuppressant, chemotherapeutic, and abortifacient agent. It is also a potent teratogen, and intentional or unintentional exposure during pregnancy is associated with heterogeneous birth anomalies. Methods: We retrospectively reviewed a cohort of patients who presented to our clinic with limb anomalies in the setting of MTX embryopathy. Results: In our case series, we describe 7 cases of patients who had limb anomalies with heterogeneous functionality, from severely debilitating to completely asymptomatic. Most of the upper extremity anomalies in our group were managed conservatively. Conclusions: Methotrexate embryopathy is a rare but clinically important entity with phenotypic and functional variability. This series underscores the need for proper counseling of patients and raises concern regarding using this medication for the purpose of abortion.
甲氨蝶呤胚胎病的极端表现
背景:甲氨蝶呤(MTX)是一种广泛应用的免疫抑制剂、化疗药物和流产剂。它也是一种强效致畸剂,妊娠期间有意或无意的接触与异质性出生异常有关。方法:我们回顾性分析了一组在MTX胚胎病中出现肢体异常的患者。结果:在我们的病例系列中,我们描述了7例具有不同功能的肢体异常患者,从严重衰弱到完全无症状。我们组的大多数上肢异常都是保守治疗的。结论:甲氨蝶呤胚胎病是一种罕见但临床上重要的实体,具有表型和功能变异性。这一系列强调了对患者进行适当咨询的必要性,并引发了人们对使用这种药物进行堕胎的担忧。
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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