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Acquired Hemophilia in an Elderly Patient with Carcinoma of the Ampulla of Vater

机译:一名老年性壶腹癌患者的获得性血友病

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摘要

Acquired hemophilia is a rare autoimmune bleeding disorder related to the production of autoantibodies that inhibit clotting factor VIII or IX. The underlying cause can be autoimmune disease, malignancy, pregnancy, or medications, but it is most commonly idiopathic. Here we present the case of an 81-year-old patient with locoregionally relapsed periampullary carcinoma who presented with soft tissue hematoma and an abnormally elevated activated partial thromboplastin time (aPTT) in the presence of a normal prothrombin time. A diagnosis of acquired hemophilia was established. The patient was managed with immunosuppressive prednisone and cyclophosphamide plus immunoglobulin G. He also received a cycle of chemotherapy with gemcitabine and oxaliplatin, because the underlying malignancy was the cause of the bleeding disorder. Care was complicated by neutropenia and nosocomial fever, but the patient eventually showed signs of clinical stability, while the aPTT decreased 2-fold. The patient was successfully discharged from the hospital and continued treatment in outpatient care.
机译:获得性血友病是一种罕见的自身免疫性出血病,与抑制凝血因子VIII或IX的自身抗体的产生有关。潜在原因可能是自身免疫性疾病,恶性肿瘤,妊娠或药物治疗,但最常见的是特发性疾病。在这里,我们介绍了一个患有局部复发性壶腹周围癌的81岁患者,该患者在正常凝血酶原时间的情况下出现软组织血肿和异常活化的部分凝血活酶时间(aPTT)升高。建立了获得性血友病的诊断。该患者接受了免疫抑制的泼尼松和环磷酰胺加免疫球蛋白G的治疗。他还接受了吉西他滨和奥沙利铂的化疗周期,因为潜在的恶性肿瘤是出血性疾病的原因。中性粒细胞减少症和医院发烧使护理变得复杂,但是患者最终表现出临床稳定的迹象,而aPTT下降了2倍。该患者已成功出院并继续接受门诊治疗。

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