A single, solid, yellow-white thymic mass was found at necropsy of a two-year-old female cynomolgus macaque from a four-week, repeatdose toxicity and immunogenicity study. Microscopically, the mass was multilobular and well encapsulated, surrounded by a thick connective tissue capsule, and composed of dense sheets of elongate or spindle-shaped cells and large cystic cavities separated by thick connective tissue stroma. Normal thymus was adjacent to the mass, but it was compressed. Within the mass were abundant interspersed Hassall's corpuscles; individual and small clusters of mature, small lymphocytes; scattered eosinophils; large areas of necrosis; focal mineralization; and cholesterol clefts. An interesting feature was the presence of large multinucleated giant cells, which varied widely in size and nuclear number. Immunohistochemical staining for two lymphocyte markers and two structural proteins confirmed the identity of the neoplastic spindle cells and other cellular components. There was no evidence of vascular invasion or metastasis. Features of the thymoma indicated it was a pre-existing condition and not treatment related.Keywords: tumors; nonhuman primate pathology; immunopathology; immune system. Thymomas are uncommon neoplasms in laboratory animals and are derived from the epithelial components of the thymus in which there are variable numbers of normal infiltrating T-and B-lymphocytes. Thymomas in veterinary medicine have been classified into lymphoid or lymphoepithelial varieties on the basis of the proportion of infiltrating lymphocytes (Valli 2007). Human medicine has used several different classification schemes based on histologic and immunophenotypic markers to distinguish resemblance to medullary or cortical regions, and the relative numbers of epithelial cells and lymphocytes (Levine and Rosai 1978;Marino and Muller-Hermelink 1985;Masaoka et al. 1981). The World Health Organization (WHO) classification system uses the shape and characteristics of the epithelial cells and the proportion of lymphocytes within the tumor to categorize them into types A, AB, B1, B2, or B3. This classification does not extend to thymic carcinoma, which is designated separately (Strobel et al. 2005). However, a recent publication employing meta-analysis of published data, which included survival times of patients with specific tumor types, found significant survival differences in only three types of tumors, A, AB, and B1 combined; B2; and B3. Their analysis also showed that different pathologists were not applying the diagnostic criteria of the WHO classification scheme consistently, even within a single ethnic group (Marchevsky et al. 2008). Moran and Suster (2008) proposed that this classification be further collapsed into just two diagnoses for benign tumors: ''thymoma'' for types A through B2, and ''atypical thymoma'' for type B3. Most authors agree that primary thymic epithelial neoplasms form part of a continuous spectrum of lesions that range from well-differentiated to poorly differentiated tumors...