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[一名母亲患有急性早幼粒细胞白血病并接受全反式维甲酸治疗的新生儿]

[A neonate born to a mother with acute promyelocytic leukemia treated by all-trans retinoic acid].

作者信息

Maeda M, Tyugu H, Okubo T, Yamamoto M, Nakamura K, Dan K

机构信息

Department of Pediatrics, Nippon Medical School.

出版信息

Rinsho Ketsueki. 1997 Sep;38(9):770-5.

PMID:9364869
Abstract

We report a female neonate delivered in week 32 of gestation by a mother who had acute promyelocytic leukemia (APL) treated by all-trans retinoic acid (ATRA). APL was diagnosed in week 29 of gestation and was treated with ATRA from week 30. Physical examination and laboratory tests showed no abnormalities at birth. The girl has since shown normal development, with no peripheral blood abnormalities at 2 years old. Hypersegmented neutrophils, which often appear during ATRA treatment, were seen in the peripheral blood of the mother and cord blood but not peripheral blood of the neonate on the day of birth. ATRA is known to cross the placenta, and has been revealed to be teratogenic in animal studies. There have been eight neonates born to the mothers with APL who were treated with ATRA during pregnancy. All infants, including this one, have shown normal growth without any complications.

摘要

我们报告了一例妊娠32周出生的女婴,其母亲患有急性早幼粒细胞白血病(APL),曾接受全反式维甲酸(ATRA)治疗。APL在妊娠29周时被诊断出来,并从妊娠30周开始接受ATRA治疗。出生时体格检查和实验室检查均未发现异常。此后,该女孩发育正常,2岁时外周血无异常。母亲外周血和脐带血中可见全反式维甲酸治疗期间常出现的多分叶中性粒细胞,但新生儿出生当天外周血中未见。已知全反式维甲酸可穿过胎盘,并且在动物研究中已显示具有致畸性。有8例母亲患有APL且在孕期接受全反式维甲酸治疗的新生儿出生。包括这例在内的所有婴儿均生长正常,无任何并发症。

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