“…FIP associated with effusion development (especially in the abdominal cavity) is the most common type of FIP encountered. 7 – 16 A range of other systemic signs can occur, such as pyrexia, inappetence, lethargy, 9 , 12 , 13 , 17 , 18 abdominal lymphadenopathy, 9 , 19 , 20 ocular signs 21 , 22 and/or neurological signs. 23 , 24 A definitive diagnosis usually relies on demonstration of the FCoV antigen or RNA in association with typical FIP histopathological changes, but a range of supporting diagnostic evidence can be obtained from haematology, serum and/or fluid sample (eg, effusion) biochemistry (eg, hyperglobulinaemia, increased alpha-1-acid glycoprotein [AGP], serum amyloid A, hyperbilirubinaemia, reduced albumin to globulin [AG] ratio), cytology (pyogranulomatous inflammation) and FCoV antigen or FCoV RNA detection (on samples such as effusions or fine-needle aspirates [FNAs]).…”