Uehara Erika, Nakao Hiro, Tsumura Yusuke, Nakadate Hisaya, Amari Shoichiro, Fujinaga Hideshi, Tsutsumi Yoshiyuki, Kang Dongchon, Ohga Shouichi, Ishiguro Akira
Department of Postgraduate Education and Training, National Center for Child Health and Development, Tokyo, Japan.
Department of General Pediatrics and Interdisciplinary Medicine, National Center for Child Health and Development, Tokyo, Japan.
AJP Rep. 2018 Apr;8(2):e68-e70. doi: 10.1055/s-0038-1639614. Epub 2018 Apr 12.
Severe protein C (PC) deficiency leads to purpura fulminans and stroke in newborns. However, the clinical impact of plasma PC activity on the development of neonatal cerebral disease remains elusive. We report a case of hemorrhagic stroke associated with neonatal asphyxia and severe PC deficiency. Plasma PC and protein S activity 7 days after birth was 12% and 43%, respectively. No mutation was found. PC levels did not exceed 20% until 2 months of age, even in the absence of consumption coagulopathy or vitamin K deficiency. Neither thromboembolic nor hemorrhagic events occurred during the infusion of activated PC concentrate (twice weekly, up to 68 days after birth). The PC activity levels gradually increased to the standard value for age by 9 months of age. The present case showed that neonatal PC deficiency without a mutation caused an intracranial hemorrhage before a slow increase in PC activity.
严重的蛋白C(PC)缺乏会导致新生儿暴发性紫癜和中风。然而,血浆PC活性对新生儿脑部疾病发展的临床影响仍不明确。我们报告一例与新生儿窒息和严重PC缺乏相关的出血性中风病例。出生7天后血浆PC和蛋白S活性分别为12%和43%。未发现突变。即使在没有消耗性凝血病或维生素K缺乏的情况下,直到2个月大时PC水平仍未超过20%。在输注活化PC浓缩物期间(每周两次,直至出生后68天),既未发生血栓栓塞事件也未发生出血事件。到9个月大时,PC活性水平逐渐升至该年龄的标准值。本病例表明,无突变的新生儿PC缺乏在PC活性缓慢升高之前导致了颅内出血。