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In utero exposure to mycophenolate mofetil: a characteristic phenotype?

机译:在子宫内暴露于霉酚酸酯:特征表型?

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Mycophenolate mofetil (MMF) is a widely prescribed immunosuppressive agent after solid organ transplantation. Potential teratogenic effects after in utero exposure to MMF in experimental studies and clinical observations in humans has been postulated in recent literature. However, a specific pattern of malformation has not been identified yet. We present a newborn patient, born to a recipient of renal transplantation, who became pregnant while taking MMF as immunosuppressive therapy. The newborn exhibited cleft lip and palate, bilateral microtia and atretic external auditory canals, chorioretinal coloboma, hypertelorism, and micrognathia. An extensive review of the literature documented six other cases with similar malformations after in utero exposure to MMF. A consistent pattern of malformations comprising cleft lip and palate, microtia and external auditory canals could be observed in five of the six cases. A different malformative pattern observed in one of the patients could be attributed to a different agent rather than MMF. The possible teratogenic effects of other immunosuppressive drugs, such as tacrolimus and prednisone, to which this patient was also exposed, are discussed herein. In addition, the differential diagnosis with other dysmorphic syndromes that can present with a similar phenotype, such as CHARGE syndrome, 18q deletion and hypertelorism-microtia-clefting (HMC) syndrome, is presented. We conclude that in utero exposure to MMF can cause a characteristic phenotype and propose the existence of a mycophenolate-associated embryopathy whose main features are: cleft lip and palate, microtia with atresia of external auditory canal, micrognathia and hypertelorism. Ocular anomalies, corpus callosum agenesis, heart defects, kidney malformations, and diaphragmatic hernia may be part of the phenotypic spectrum of MMF embryopathy. The human teratogenicity of MMF is reinforced by this report, and the current contraceptive recommendations about its use in fertile women are stressed.
机译:霉酚酸酯(MMF)是固体器官移植后广泛使用的免疫抑制剂。在最近的文献中已经提出了在子宫内MMF暴露于人的实验研究和临床观察中的潜在致畸作用。但是,尚未发现畸形的特定模式。我们介绍了一名新生儿患者,该患者出生于肾移植患者,在接受MMF作为免疫抑制治疗时怀孕。新生儿表现出唇left裂,双侧小口畸形和闭锁性外耳道,脉络膜视网膜结肠炎,肥大性和微棘皮症。广泛的文献回顾记录了子宫内暴露于MMF后的其他六例具有类似畸形的病例。在六例中的五例中,可以观察到一致的畸形,包括唇裂和pa裂,小口畸形和外耳道。在其中一名患者中观察到的不同畸形模式可以归因于一种不同的因素而不是MMF。本文还讨论了该患者也接触过的其他免疫抑制药物(如他克莫司和泼尼松)的可能的致畸作用。此外,提出了与其他具有类似表型的畸形综合症的鉴别诊断,例如CHARGE综合症,18q缺失和过度精症-小眼症(HMC)综合症。我们得出的结论是,在子宫内暴露于MMF会导致特征性表型,并提出了霉酚酸酯相关的胚胎病的存在,其主要特征是:唇,裂,外耳道闭锁性小口畸形,微念头症和超视力。眼部异常,call体发育不全,心脏缺损,肾脏畸形和diaphragm肌疝可能是MMF胚胎表型的一部分。该报告加强了MMF的人为致畸性,并强调了当前有关在可育妇女中使用MMF的避孕建议。

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