病理
骨髓
多发性骨髓瘤
免疫组织化学
免疫球蛋白D
川地34
免疫固定
浆细胞瘤
基因重排
浆细胞肿瘤
免疫分型
血清蛋白电泳
生物
单克隆
抗体
医学
抗原
B细胞
单克隆抗体
免疫学
生物化学
遗传学
干细胞
基因
作者
Ian J. Wachowiak,A Russell Moore,Anne C. Avery,Forgivemore Magunda,Adam Harris,Hannah Laurence,Christopher M. Fulkerson,Caroline V. Fulkerson,Joanne B. Messick,Natalia J. Strandberg,Stephanie McGrath
标识
DOI:10.1177/03009858221087637
摘要
Three dogs under 12 months old were diagnosed with atypical multiple myeloma (MM), having an aggressive multifocal anaplastic round cell sarcoma in bone marrow, viscera, and/or peripheral blood, which were confirmed by cytology and immunohistochemistry to be of plasma cell origin. The intramedullary sarcomas caused myelophthisis, osteolysis, and hypercalcemia. Complete or free light chain monoclonal gammopathy in the serum and/or urine was demonstrated by protein electrophoresis and immunofixation. The polymerase chain reaction for antigen receptor rearrangement assay performed on 2 cases identified a clonally rearranged immunoglobulin gene. Neoplastic cells lacked expression of CD45, CD3, CD18, CD21, CD34, and MHCII by flow cytometry. Immunohistochemistry revealed MUM1 immunoreactivity of the neoplastic cells. Combining all data, the diagnosis was MM. An aggressive form of MM in young dogs should be a differential diagnosis for patients with an immunoglobulin-productive, B cell-clonal, CD45-negative, MUM1-positive discrete cell neoplasm arising from the bone marrow.
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