Abstract. Pancreatic tissues from 93 adult domestic cats with no clinicopathologic evidence of overt diabetes mellitus were examined for islet amyloid. Amyloid deposits were found in the pancreatic islets of 44 cats. Approximately one-third of these deposits were not seen with HE, but subsequently were identified with Congo red stain. The proportion of islets with amyloid, the intra-islet location of amyloid, and the amount of amyloid in individual islets also were characterized. In this select population of adult cats, the presence or absence of islet amyloid was not linked significantly (p = > 0.05) to age, breed, sex or primary anatomic diagnosis. Results of this study indicate that: the incidence of islet amyloid in cats is higher than previously recognized; as in man, islet amyloid can occur in cats without concurrent overt diabetes mellitus; and islet amyloid should not be considered pathognomonic for diabetes mellitus.Pancreatic islet amyloid deposits (i.e., insular amyloid) occur in man [2,3,4, 131, non-human primates [7,8, 171, raccoons [ 11, 151, and domestic and wild cats [5, 10, 11, 121. Insular amyloid in man and animals often is associated with maturityonset diabetes mellitus and is rare in juvenile-onset diabetes. A majority of human diabetics over 50 years old have amyloid deposits in their pancreatic islets [I, 4, 13, 201, but insular amyloid also has been identified in a significant number of aged, non-diabetic people [3,4,25]. The amount and frequency of insular amyloid increases with age in both diabetic and non-diabetic people [2,3].A significant relationship exists between the presence of insular amyloid and maturity-onset diabetes, but it is not known whether the amyloid causes diabetes, or arises secondarily to it. Studies of insular amyloid in man indicate that: amyloid deposits are limited to the pancreatic islets [23]; deposition apparently is independent of amyloid in other organs [21]; and systemic (primary or secondary) amyloidosis seems to have no facilitating effect on the formation of insular amyloid [21]. Histochemical, biochemical, and clinicopathologic differences between insular and systemic amyloid imply different and independent mechanisms of formation. Major precursor substances for systemic amyloid are immunoglobulin light chains in primary and myeloma-associated amyloidosis [6], and serum protein AA in secondary 310