Objective: To evaluate the incidence, etiology and progression of Pigmentary keratitis in dogs. Materialsand Methods: A total of 83 corneas from 55 dogs of different breeds, sex and age were selected for the study. Signalment, anamnesis, nature of discharge and duration of illness was collected from all the animals.The progression of pigmentation was assessed by dividing the cornea in to four quadrants. Pigmentation grading, extent of pigmentation and mean pigment density were calculated by dividing the cornea in to 24 sectors. Schirmer tear test (STT), fluorescein dye test (FDT), tonometry, and slitlamp biomicroscopy and Cornealimpression cytology were done. Results: Among the 55 animals, 51 dogs were Chinese Pug (92.7%) and the mean age was 33.13 ± 3.12 months. Among 55 animals, 28 were females (50.9%) and left cornea was affected in 44 animals (53.01%). The mean duration of the disease as noticed by the owner was 07.21 ± 0.65 months.Most of the owners were totally unaware about the condition of the eye. Among 83 corneas, 40 (35%) showed pigmentation in all the sectors. 29 animals (53%) wereaffected with keratoconjunctivitis sicca (KCS) followed by 13 animals (24%) affected with entropion. The mean value of random blood sugar was 107.84 ± 0.99 and the mean intraocular pressure in the animals under the study was 40.64 ± 2.38. The mean value of pigmentation grading,extent of pigmenta ion and mean pigment density was 32.59 ± 2.27, 15.67 ± 0.83 and 1.37 ± 0.07 respectively. The mean value of Schirmer tear test was 10.31 ± 0.58 andunder high power microscopy, Leishman’s stained corneal impression cytology revealed infiltration of neutrophils in all the slides. Conclusion: It was concludedthat Chinese pugs under the age of 3 years are mostly affected and females and left eye is mostly affected. All the animals with pigmentation is having KCS.

Objective-To validate a radioimmunoassay for measurement of procollagen type III amino terminal propeptide (PIIINP) concentrations in canine serum and bronchoalveolar lavage fluid (BALF) and investigate the effects of physiologic and pathologic conditions on PIIINP concentrations. Sample Population-Sera from healthy adult (n = 70) and growing dogs (20) and dogs with chronic renal failure (CRF; 10), cardiomyopathy (CMP; 12), or degenerative valve disease (DVD; 26); and sera and BALF from dogs with chronic bronchopneumopathy (CBP; 15) and healthy control dogs (10 growing and 9 adult dogs). Procedure-A radioimmunoassay was validated, and a reference range for serum PIIINP (S-PIIINP) concentration was established. Effects of growth, age, sex, weight, CRF, and heart failure on S-PIIINP concentration were analyzed. In CBP-affected dogs, S-PIIINP and BALF-PIIINP concentrations were evaluated. Results-The radioimmunoassay had good sensitivity, linearity, precision, and reproducibility and reasonable accuracy for measurement of S-PIIINP and BALF-PIIINP concentrations. The S-PIIINP concentration reference range in adult dogs was 8.86 to 11.48 microgram/L. Serum PIIINP concentration correlated with weight and age. Growing dogs had significantly higher S-PIIINP concentrations than adults, but concentrations in CRF-, CMP-, DVD-, or CBP-affected dogs were not significantly different from control values. Mean BALF-PIIINP concentration was significantly higher in CBP-affected dogs than in healthy adults. Conclusions and Clinical Relevance-In dogs, renal or cardiac disease or CBP did not significantly affect S-PIIINP concentration; dogs with CBP had high BALF-PIIINP concentrations. Data suggest that the use of PIIINP as a marker of pathologic fibrosis might be limited in growing dogs.