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与产前接触苯妥英和甲基苯巴比妥相关的室管膜母细胞瘤。

Ependymoblastoma associated with prenatal exposure to diphenylhydantoin and methylphenobarbitone.

作者信息

Lipson A, Bale P

出版信息

Cancer. 1985 May 1;55(9):1859-62. doi: 10.1002/1097-0142(19850501)55:9<1859::aid-cncr2820550902>3.0.co;2-f.

DOI:10.1002/1097-0142(19850501)55:9<1859::aid-cncr2820550902>3.0.co;2-f
PMID:3978571
Abstract

Ependymoblastoma developed in a 28-month-old girl whose epileptic mother took diphenylhydantoin and methylphenobarbitone throughout pregnancy. The child was also shown to be a genetic carrier for ornithine transcarbamylase deficiency, an x-linked inborn error of urea cycle metabolism. The possibility of transplacental carcinogenesis should be considered, as other juvenile embryonic tumors such as neuroblastoma, melanotic neuroectodermal tumor, and mesenchymoma have been reported in offspring after diphenylhydantoin use by the mother during pregnancy.

摘要

一名28个月大的女孩患上了室管膜母细胞瘤,其患有癫痫的母亲在整个孕期都服用苯妥英钠和甲基苯巴比妥。该患儿还被证明是鸟氨酸转氨甲酰酶缺乏症的基因携带者,这是一种X连锁的尿素循环代谢先天性缺陷。应考虑经胎盘致癌的可能性,因为有报道称,母亲在孕期使用苯妥英钠后,其后代出现了其他青少年胚胎性肿瘤,如神经母细胞瘤、黑色素性神经外胚层肿瘤和间叶瘤。

相似文献

1
Ependymoblastoma associated with prenatal exposure to diphenylhydantoin and methylphenobarbitone.与产前接触苯妥英和甲基苯巴比妥相关的室管膜母细胞瘤。
Cancer. 1985 May 1;55(9):1859-62. doi: 10.1002/1097-0142(19850501)55:9<1859::aid-cncr2820550902>3.0.co;2-f.
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Malignant mesenchymoma and birth defects. Prenatal exposure to phenytoin.恶性间叶瘤与出生缺陷。产前接触苯妥英。
JAMA. 1977 Jul 25;238(4):334-5.
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[Haemorrhagic diathesis in a newborn child of a mother on anti-epileptic medication (author's transl)].母亲服用抗癫痫药物的新生儿的出血素质(作者译)
Dtsch Med Wochenschr. 1974 Jun 14;99(24):1315-7. doi: 10.1055/s-0028-1107939.
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Synaptophysin expression in "ependymal tumors" induced by ethyl-nitrosourea in rats.大鼠中由乙基亚硝基脲诱导的“室管膜瘤”中突触素的表达。
Am J Pathol. 1992 Nov;141(5):1037-41.
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Problems in transplacental carcinogenesis.
Indian J Cancer. 1975 Mar;12(1):21-9.
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[Genetic counseling in ornithine carbamoyltransferase deficiency].
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Prenatal counseling in heterozygotes for ornithine transcarbamylase deficiency.鸟氨酸转氨甲酰酶缺乏症杂合子的产前咨询
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A case with combined rare inborn metabolic disorders: congenital adrenal hyperplasia and ornithine transcarbamylase deficiency.一个合并罕见先天性代谢紊乱的病例:先天性肾上腺皮质增生症和鸟氨酸转氨甲酰酶缺乏症。
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引用本文的文献

1
The United Kingdom Childhood Cancer Study: objectives, materials and methods. UK Childhood Cancer Study Investigators.英国儿童癌症研究:目标、材料与方法。英国儿童癌症研究调查人员
Br J Cancer. 2000 Mar;82(5):1073-102. doi: 10.1054/bjoc.1999.1045.
2
Family studies in ornithine transcarbamylase deficiency.鸟氨酸转氨甲酰酶缺乏症的家系研究。
Arch Dis Child. 1988 Mar;63(3):297-302. doi: 10.1136/adc.63.3.297.
3
Potential risk factors for brain tumors in children. An analysis of 200 cases.儿童脑肿瘤的潜在风险因素。200例病例分析。
Childs Nerv Syst. 1990 Jan;6(1):8-12. doi: 10.1007/BF00262258.