Kelesidis Theodoros, Raphael Jonelle, Blanchard Elizabeth, Parameswaran Rekha
Department of Medicine, Caritas St Elizabeth's Medical Center, Tufts University School of Medicine, Boston, MA, USA.
J Med Case Rep. 2010 Jul 29;4:231. doi: 10.1186/1752-1947-4-231.
Acquired factor VIII deficiency is a rare entity that can lead to severe and life-threatening bleeding. We describe a case of severe bleeding from the tongue secondary to acquired hemophilia and discuss treatment options, including aminocaproic acid and recombinant factor VIII, which have not been widely reported in the literature for the management of such patients.
A 94-year-old Caucasian man presented to our institution with diffuse bruising and extensive bleeding from the tongue secondary to mechanical trauma. He had no prior history of bleeding and his medical history was unremarkable except for dementia and hypertension. Coagulation studies revealed a prolonged activated partial thromboplastin time and a mixing study was consistent with the presence of an inhibitor. Quantitative assays revealed a reduced level of factor VIII activity (1%) and the presence of a factor VIII inhibitor, measured at seven Bethesda units, in the serum. Oral prednisone therapy (60mg/day) was given. He also received intravenous aminocaproic acid and human concentrate of factor VIII (Humate-P) and topical anti-thrombolytic agents (100 units of topical thrombin cream). His hospital course was prolonged because of persistent bleeding and the development of profuse melena. He required eight units of packed red blood cells for transfusion. Hospitalization was also complicated by bradycardia of unclear etiology, which started after infusion of aminocaproic acid. His activated partial thromboplastin time gradually normalized. He was discharged to a rehabilitation facility three weeks later with improving symptoms, stable hematocrit and resolving bruises.
Clinicians should suspect a diagnosis of acquired hemophilia in older patients with unexplained persistent and profound bleeding from uncommon soft tissues, including the tongue. Use of factor VIII (Humate-P) and aminocaproic acid can be useful in this coagulopathy but clinicians should be aware of possible life-threatening side effects in older patients, including bradycardia.
获得性因子 VIII 缺乏症是一种罕见的疾病,可导致严重的、危及生命的出血。我们描述了一例因获得性血友病导致舌部严重出血的病例,并讨论了治疗方案,包括氨基己酸和重组因子 VIII,这些治疗方法在文献中尚未广泛报道用于此类患者的管理。
一名 94 岁的白种男性因机械性创伤导致舌部广泛出血和全身瘀斑就诊于我院。他既往无出血史,除痴呆和高血压外,病史无明显异常。凝血研究显示活化部分凝血活酶时间延长,混合试验结果与存在抑制剂相符。定量分析显示因子 VIII 活性水平降低(1%),血清中因子 VIII 抑制剂水平为 7 贝塞斯达单位。给予口服泼尼松治疗(60mg/天)。他还接受了静脉注射氨基己酸、人凝血因子 VIII 浓缩物(Humate-P)和局部抗纤溶药物(100 单位局部凝血酶乳膏)。由于持续出血和大量黑便的出现,他的住院时间延长。他需要输注 8 单位的浓缩红细胞。住院期间还出现了病因不明的心动过缓,在输注氨基己酸后开始出现。他的活化部分凝血活酶时间逐渐恢复正常化。三周后,他症状改善、血细胞比容稳定、瘀斑消退,出院转至康复机构。
临床医生应怀疑老年患者出现不明原因的持续且严重的罕见软组织出血(包括舌部出血)时可能患有获得性血友病。使用因子 VIII(Humate-P)和氨基己酸对这种凝血病可能有效,但临床医生应意识到老年患者可能出现危及生命的副作用,包括心动过缓。