Hamilton M, French W, Rhymes N, Collins P
Haematology Department, University Hospital of Wales, Cardiff, UK.
Haemophilia. 2006 Jul;12(4):441-3. doi: 10.1111/j.1365-2516.2006.01291.x.
We present two patients with severe haemophilia A, who presented with haemorrhagic shock, secondary to a liver haematoma in the neonatal period. Both required emergency treatment and diagnosis of the hereditary coagulation defect. Major organ bleeding in severe haemophilia A in the newborn period is rare, and this unusual complication is not well recognized. Failure to recognize that the bleeding is due to a bleeding disorder, particularly in the absence of a family history, may lead to delay in appropriate management.
我们报告了两名患有严重甲型血友病的患者,他们在新生儿期因肝脏血肿继发出血性休克。两人均需要紧急治疗并诊断遗传性凝血缺陷。新生儿期严重甲型血友病出现主要器官出血的情况罕见,这种不寻常的并发症尚未得到充分认识。未能认识到出血是由出血性疾病引起的,尤其是在没有家族病史的情况下,可能会导致适当治疗的延迟。