Wanless I R, Gryfe A
Arch Pathol Lab Med. 1986 Apr;110(4):331-5.
A case of hereditary hemorrhagic telangiectasia with prominent nodular transformation of the liver is described. The presence of enlarged arteries was documented morphometrically. Artery-to-portal vein shunts were also found. The association of abnormal vessels with hepatic nodules supports the hypothesis that abnormalities of blood flow cause nodular transformation. Nodular transformation may be the lesion that has heretofore been termed cirrhosis hepatis telangiectasia or atypical cirrhosis.
本文描述了一例伴有明显肝脏结节样转化的遗传性出血性毛细血管扩张症病例。通过形态测量法证实了肝动脉增粗。还发现了动脉-门静脉分流。异常血管与肝结节的关联支持了血流异常导致结节样转化的假说。结节样转化可能就是迄今被称为肝毛细血管扩张性肝硬化或非典型肝硬化的病变。