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    題名: RET protooncogene mutations in patients with apparently sporadic medullary thyroid carcinoma
    作者: Huang, CN;Wu, SL;Chang, TC;Huang, SH;Chang, TJ
    貢獻者: 醫學院醫學系生化學科;Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan;Natl Taiwan Univ, Coll Med, Dept Internal Med, Taipei, Taiwan;Natl Taiwan Univ, Coll Med, Dept Surg, Taipei 10018, Taiwan;China Med Coll, Dept Biochem, Taichung, Taiwan;Natl Chung Hsing Univ, Coll Agr, Dept Vet Med, Taichung 40227, Taiwan
    日期: 1998
    上傳時間: 2010-09-24 14:53:46 (UTC+8)
    出版者: EXCERPTA MEDICA ASIA LTD
    摘要: BACKGROUND: Ebstein anomaly is a rare tricuspid valve anomaly. Some fetuses with Ebstein's anomaly have concurrent severe cardiac function impairment, which results in hydrops fetalis. Most of these fetuses are inevitably terminally ill. No reports have demonstrated the potential prenatal therapy for fetuses under such conditions. CASE: Ebstein's anomaly and hydrops fetalis were detected at 28 weeks' gestation. Tricuspid regurgitation with congestive heart failure was observed. From 28 to 34 weeks' gestation, intrauterine therapy with digoxin, 0.75 mg/d, was administered. The fetal hydrops status improved gradually, while the tricuspid valve regurgitation persisted. At 36 weeks' gestation the fetus was delivered normally. During the neonatal phase, digoxin was continued adn gradually tapered off. The tricuspid valve regurgitation and cardiomegaly gradually improved. CONCLUSIONS: The favorable outcome in this case supports the positive effect of prenatal digoxin therapy for Ebstein's anomaly with hydrops fetalis. In such conditions, upon the appearance of hydrops and congestive cardiac failure, immediate digoxin therapy may be useful. This successful trial encouraged us to manage such fetuses more aggressively.
    關聯: JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 97(8):541-546
    顯示於類別:[醫學系] 期刊論文

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