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Multiple acquired portosystemic shunts secondary to primary hypoplasia of the portal vein in a cat

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 portosyste...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021884/
https://www.ncbi.nlm.nih.gov/pubmed/29628453
http://dx.doi.org/10.1292/jvms.17-0648
Descripción
Sumario: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.