A 13-year-old FS DSH cat was presented for the evaluation of polyuria and polydipsia of several months’ duration. The serum biochemical profile revealed marked hyperglycemia. The CBC showed a low RBC count, lymphopenia, and a monocytosis. The TT4 and free T4 were within normal limits. A fructosamine level was high. The urinalysis showed glucosuria, and hematuria. The urine culture was negative for bacterial growth. A fructosamine level was repeated a few months later and remained elevated. Insulin-like Growth Factor 1 was normal, and a diagnosis of acromegaly was considered unlikely.
A 13-year-old FS DSH cat was presented for the evaluation of polyuria and polydipsia of several months’ duration. The serum biochemical profile revealed marked hyperglycemia. The CBC showed a low RBC count, lymphopenia, and a monocytosis. The TT4 and free T4 were within normal limits. A fructosamine level was high. The urinalysis showed glucosuria, and hematuria. The urine culture was negative for bacterial growth. A fructosamine level was repeated a few months later and remained elevated. Insulin-like Growth Factor 1 was normal, and a diagnosis of acromegaly was considered unlikely. A recheck of the blood work revealed hyperglycemia, hyperphosphatemia, hypokalemia and hyperlipasemia. The CBC showed elevations of the MCH and MCHC, as well as thrombocytopenia. The results of an ACTH stimulation were suggestive of hyperadrenocorticism. The urine had a turbid appearance on the urinalysis and showed proteinuria, hematuria, and elevated RBCs microscopically. The urine culture was negative. Vitamin B12, folate concentrations were performed and the the folate was found to be elevated. High fTLI and a high PLI were also present. Fructosamine levels were now within normal limits.