Esophageal atresia and prenatal exposure to mycophenolate

被引:10
|
作者
Martin, M. C. [1 ,6 ]
Cristiano, E. [2 ,6 ]
Villanueva, M. [3 ]
Bonora, M. L. [4 ,6 ]
Berguio, N. [6 ]
Tocci, A. [5 ,6 ]
Groisman, B. [1 ,6 ]
Bidondo, M. P. [1 ,6 ]
Liascovich, R. [1 ,6 ]
Barbero, P. [1 ,6 ]
机构
[1] Natl Ctr Med Genet Dr Eduardo Castilla, Buenos Aires, DF, Argentina
[2] Penna Hosp, Serv Neonatol, Buenos Aires, DF, Argentina
[3] Elizalde Hosp, Med Genet Serv, Buenos Aires, DF, Argentina
[4] Reg Hosp Rio Cuarto, Serv Neonatol, Cordoba, Argentina
[5] Argerich Hosp, Serv Neonatol, Buenos Aires, DF, Argentina
[6] Natl Registry Congenital Anomalies Argentina RENA, Buenos Aires, DF, Argentina
关键词
Mycophenolate mofetil; Drug induced abnormalities; Teratogen; Esophageal atresia; HEMIFACIAL MICROSOMIA; MOFETIL EMBRYOPATHY; CONSEQUENCE; ACID;
D O I
10.1016/j.reprotox.2014.10.015
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mycophenolate mofetil is a widely prescribed immunosuppressive agent for transplant patients and autoimmune diseases. Potential teratogenic effects after in utero exposure to mycophenolate mofetil has been described in human clinical observations. The complete clinical pattern is still being delineated. We present four newborns with esophageal atresia and other congenital anomalies, prenatally exposed to mycophenolate mofetil during the first trimester. Two of the cases had other defects related to the embryopathy: microtia, eye abnormalities and oral clefts. Two cases did not show major craniofacial anomalies. We propose that esophageal atresia with or without tracheoesophageal fistula is a feature of mycophenolate embryopathy even without the presence of other major craniofacial anomalies. The human teratogenicity of MMF is reinforced by this report, and the current contraceptive recommendations about its use in fertile women are stressed. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:117 / 121
页数:5
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