Hardy T J, Myerowitz R L, Bender B L
Arch Pathol Lab Med. 1979 Oct;103(11):583-5.
A patient had systemic amyloidosis that extensively involved the lungs and breasts. Diffuse parenchymal pulmonary amyloidosis is rare but well described. Involvement of the breast in systemic amyloidosis is, however, most unusual. This patient's amyloidosis was associated with diffuse plasmacytosis and a kappa-chain gammopathy. The plasmacytosis was most prominent in the renal interstitium. Immunoperoxidase staining of the renal infiltrate and breast demonstrated IgG/kappa-staining plasma cells exclusively, suggesting that these cells were a monoclonal proliferation that contributed to the patient's M-protein and possibly to the patient's amyloid deposits.
一名患者患有系统性淀粉样变性,广泛累及肺部和乳房。弥漫性实质性肺淀粉样变性罕见但已有充分描述。然而,系统性淀粉样变性累及乳房极为罕见。该患者的淀粉样变性与弥漫性浆细胞增多症和κ链丙种球蛋白病有关。浆细胞增多症在肾间质最为显著。对肾脏浸润灶和乳房进行免疫过氧化物酶染色显示仅存在IgG/κ染色的浆细胞,提示这些细胞是单克隆增殖,与患者的M蛋白有关,可能也与患者的淀粉样沉积物有关。