Isobe T, Hata S, Murakami M, Kadowaki S, Fujita T
Jpn J Med. 1984 Aug;23(3):254-7. doi: 10.2169/internalmedicine1962.23.254.
A 74 yo female was found to have bullous dermal amyloidosis on the background of systemic amyloidosis with multiple myeloma. There was monoclonal immunoglobulin light chain of kappa type in the serum with no proteinuria (Bence Jones proteinemia without Bence Jones proteinuria), along with proliferations of kappa-producing plasma cells in the marrow.
一名74岁女性在患有多发性骨髓瘤的系统性淀粉样变性背景下被发现患有大疱性皮肤淀粉样变性。血清中有κ型单克隆免疫球蛋白轻链，无蛋白尿（本斯·琼斯蛋白血症但无本斯·琼斯蛋白尿），同时骨髓中有产生κ的浆细胞增殖。
