Congenital Portosystemic Shunt and Staghorn Nephrolithiasis in a Yorkshire Terrier
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A 4 year old female spayed Yorkshire terrier was presented to Cornell’s Internal Medicine Service for evaluation of bilateral nephrolithiasis and a possible portosystemic shunt. She was initially presented to her primary care veterinarian for chronic intermittent vomiting and polydipsia. Abdominal radiographs disclosed bilateral (mineralized) nephroliths. Bloodwork disclosed reduced albumin and blood urea nitrogen (BUN) concentrations and increased liver enzyme activity (ALT, AST). Pre- and post-prandial bile acid concentrations were markedly increased. Additional diagnostic testing demonstrated a subnormal Protein C activity, (59%, reference range 75-135%). An abdominal ultrasound and computed tomographic angiography (CT-A) confirmed a splenophrenic portosystemic shunt. Shunt ligation with intraoperative portograms (pre & post portal vein attenuation) and monitoring splanchnic portal pressure suggested low risk of post-operative portal hypertension with complete shunt attenuation. The splenophrenic extrahepatic shunt was completely ligated. Staghorn nephroliths were surgically removed via bilateral nephrotomy. Surgical treatment was successful with subsequent normalization of liver enzyme & Protein C activity as well as concentrations of albumin and BUN. The dog continues to do well at home.