Daly J J, Schiller A L
Am J Med. 1976 May 10;60(5):723-6. doi: 10.1016/0002-9343(76)90510-6.
The livers of four patients with hereditary hemorrhagic telangiectasia--including the original case of Osler--were examined at autopsy. Characteristic random focal fibrovascular lesions were found in all. The importance of recognizing the apparently common and seemingly benign hepatic involvement in this disease is emphasized in view of its possible confusion with more serious types of liver disease that may complicate the condition.
对四名遗传性出血性毛细血管扩张症患者的肝脏进行了尸检,其中包括奥斯勒最初报道的病例。在所有患者的肝脏中均发现了特征性的随机局灶性纤维血管病变。鉴于这种疾病中明显常见且看似良性的肝脏受累可能与更严重的、可能使病情复杂化的肝病类型相混淆,因此强调了认识这一点的重要性。