イトウ ナオコ
Itou Naoko
井藤 奈央子 所属 医学部 医学科(東京女子医科大学病院) 職種 助教 |
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論文種別 | 症例報告 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Neonatal asphyxia and renal failure as the presentation of non-inherited protein C deficiency. |
掲載誌名 | 正式名:Journal of perinatology : official journal of the California Perinatal Association 略 称:J Perinatol ISSNコード:14765543/07438346 |
掲載区分 | 国外 |
巻・号・頁 | 33(3),pp.239-41 |
著者・共著者 | Matsunaga Y, Ohga S, Kinjo T, Ochiai M, Ito N, Doi T, Kang D, Hara T |
発行年月 | 2013/03 |
概要 | Inherited or acquired protein C (PC) deficiency leads to thromboembolic events. Plasma PC activity in infancy is physiologically lower than in adults. We describe a case of neonatal asphyxia and acute renal failure associated with isolated PC deficiency. A full-term male infant was born to a healthy mother by caesarean section because of fetal distress. The small-for-gestational age infant showed 2 and 7 of Apgar scores at 1 and 5 minutes, respectively. Hypercoagulability required repeated infusions of fresh frozen plasma. Coagulation study revealed PC activity, 6%, protein S activity, 61%, and high D-dimer levels, along with normal factor VII activity and absent vitamin K deficiency. Anticoagulant and activated PC therapy improved coagulopathy and nephropathy. Imaging analyses indicated no visceral infarctions. Renal function and PC activity have been slowly normalized until 6 months of age. He had no PROC mutation or PC-deficient parents. Selective PC deficiency may occur as an acquired cause of hypercoagulable crisis in the stressed newborn. |
DOI | 10.1038/jp.2012.55 |
PMID | 23443294 |