Abstract. Extramedullary plasmacytomas were studied in 29 dogs. The site at which tumors occurred and the age and sex of the dogs were similar to those in previous reports. The skin of the digits, chin, ear, and lip represented the most common (17/29) tumor sites. Males and females were equally represented, and tumors occurred in middle-aged to old dogs (mean age, 9.0 years). A breed predilection was seen in the Cocker Spaniel (n = 7; 24%); Cocker Spaniels represented only 4% (210/4,725) of the submissions during the same period. Tumors were stained with immunohistochemical markers (λ light chain, K light chain) and thioflavine T. Immunoreactivity was limited to either λ or K light chains, consistent with a monoclonal plasma cell population. The majority of tumors expressed λ light chains, consistent with previously reported canine plasma cell dyscrasias. Thioflavine T cytoplasmic fluorescence was seen in the majority (18/29) of plasmacytomas and with inflammatory plasma cells present in control specimens. Other round cell neoplasms (lymphosarcoma, histiocytoma, and mastocytoma) were negative with thioflavine T, indicating that positive staining with thioflavine T was specific for plasma cells (neoplastic and inflammatory). This study confirms by immunohistochemistry that canine extramedullary plasmacytomas disproportionately express λ light chains and establishes thioflavine T staining as a rapid histochemical method for diagnosis of these tumors.The morphologic, clinical, and biological features of canine extramedullary plasmacytoma (EMP) have been reported 1,13,16,17,20,24 Most dogs were aged adults, and tumors developed most commonly on the mucocutaneous junction of the mouth, the skin between the digits, and on the external ear. 1,24 More than 90% of the dogs with cutaneous EMP were cured by surgical excision, indicating that these tumors were most likely benign. Multiple EMP were found in a small percentage of dogs but were not associated with progression to multiple myeloma. Only rarely did cases of canine EMP precede the development of multiple myeloma, 14,24 which is different from the clinical course seen in humans.In humans, long-term survival of 15 years without recurrence occurs in the majority of cases of EMP, 28 but in approximately 25% of the cases, EMP will develop into multiple myeloma. 18 When EMP precedes the development of multiple myeloma, an extended period (up to 10 years) may occur before clinical signs of bone involvement are noted. Secondary extramedullary involvement of the skin with primary multiple myeloma is rare. Immunohistochemical characterization of human EMP with immunoglobulin heavy and light chains reveals a monoclonal proliferation of plas-