Mori K, Ishimura E, Goto H, Shoji S, Seki S, Yamashita T, Wakasa K, Nishizawa Y, Morii H
Second Department of Internal Medicine, Osaka City University Medical School, Japan.
J Gastroenterol. 1996 Feb;31(1):123-8. doi: 10.1007/BF01211199.
Idiopathic portal hypertension (IPH) is a condition marked by unexplained portal hypertension. Although a number of immunological abnormalities occur in patients with IPH, liver function is usually normal. We experienced an unusual case of IPH in a 49-year-old woman, who had pronounced splenomegaly. Laboratory data revealed pancytopenia, hypergammaglobulinemia, and liver dysfunction. Antinuclear antibodies were positive, with high titer at 1280 dilutions of sera. LE cell phenomena were also positive. Histological examination of biopsied liver showed only mild changes, but portal venous pressure was markedly elevated, at 38 cm H2O. This case was thus characterized by both a high serum titer of autoantibodies and liver dysfunction.
