Department of Surgery, Jichi Medical University, 3311-1 Shimotsuke, Tochigi 329-0498, Japan.
Surg Today. 2013 Jun;43(6):670-4. doi: 10.1007/s00595-012-0290-x. Epub 2012 Aug 14.
We report a case of acquired hemophilia A (AHA) after esophageal resection. The patient was an 80-year-old woman whose preoperative activated partial-thromboplastin time (APTT) was well within the normal range, at 34.9 s. She underwent thoracic esophagectomy and gastric pull-up for superficial esophageal cancer (operative time, 315 min; intraoperative blood loss, 245 ml). Intrathoracic and subcutaneous bleeding occurred spontaneously on postoperative day (POD) 39. The APTT was prolonged, at 140 s, and factor VIII inhibitor was 36 Bethesda U/ml. Treatment with recombinant activated factor VII, prednisolone, and cyclophosphamide resulted in remission within 2 months. This case supports an association between surgery and the triggering of factor VIII inhibitors. The diagnosis of AHA requires clinical acumen and must be considered in any patient with bleeding and a prolonged APTT.
我们报告一例获得性血友病 A(AHA)病例,该病例发生于食管切除术后。患者为 80 岁女性,术前活化部分凝血活酶时间(APTT)在正常范围内,为 34.9s。患者因食管浅表癌行胸腔镜食管切除术和胃上提术(手术时间 315 分钟,术中出血量 245ml)。术后第 39 天自发性出现胸内和皮下出血。APTT 延长至 140s,VIII 因子抑制剂为 36Bethesda U/ml。采用重组活化因子 VII、泼尼松和环磷酰胺治疗,2 个月内病情缓解。该病例提示手术与 VIII 因子抑制剂的触发之间存在关联。AHA 的诊断需要临床敏锐性,任何有出血和 APTT 延长的患者都必须考虑该病。