Sugimoto Satoko, Maeda Shingo, Tsuboi Masaya, Saeki Kohei, Chambers James K, Yonezawa Tomohiro, Fukushima Kenjiro, Fujiwara Reina, Uchida Kazuyuki, Tsujimoto Hajime, Matsuki Naoaki, Ohno Koichi
Department of Veterinary Internal Medicine, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
J Vet Med Sci. 2018 Jun 6;80(6):874-877. doi: 10.1292/jvms.17-0648. Epub 2018 Apr 9.
A 6-year 5-month-old spayed female Scottish Fold cat presented with a one-month history of gait abnormalities, increased salivation, and decreased activity. A blood test showed hyperammonemia and increased serum bile acids. Imaging tests revealed multiple shunt vessels indicating acquired portosystemic shunt. Histopathologic analysis of liver biopsy showed features consistent with liver hypoperfusion, such as a barely recognizable portal vein, increased numbers of small arterioles, and diffuse vacuolar degeneration of hepatocytes. These findings supported the diagnosis of primary hypoplasia of the portal vein/microvascular dysplasia, (PHPV/MVD). To our knowledge, this is the first case of feline PHPV/MVD that developed multiple acquired portosystemic shunts and presented with hepatic encephalopathy.
一只6岁5个月大已绝育的雌性苏格兰折耳猫出现了为期一个月的步态异常、唾液分泌增多和活动减少的症状。血液检查显示高氨血症和血清胆汁酸升高。影像学检查发现多处分流血管,提示存在后天性门体分流。肝脏活检的组织病理学分析显示出与肝脏灌注不足相符的特征,如门静脉几乎难以辨认、小动脉数量增加以及肝细胞弥漫性空泡变性。这些发现支持了门静脉原发性发育不全/微血管发育异常(PHPV/MVD)的诊断。据我们所知,这是首例发生多处后天性门体分流并伴有肝性脑病的猫PHPV/MVD病例。