Colović Natasa, Terzić Tatjana, Andelić Bosko, Sretenović Mirjana, Mihaljević Biljana, Lipkovski Jasmina Marković, Colović Milica
Institute of Hematology, Clinical Center of Serbia, Belgrade, Serbia.
Med Oncol. 2008;25(4):458-61. doi: 10.1007/s12032-008-9048-0. Epub 2008 Jan 24.
Two patients with lymphoplasmacytic lymphoma, and monoclonal proteins of IgM in one, and IgG and lambda light chains in the second patient, nephrotic syndrome and acute renal failure are reported. A 58-year-old man previously treated for pre-B acute lymphoblastic leukemia, developed 3 years later nephrotic syndrome as a complication of lymphoplasmacytic lymphoma and high-paraprotein IgM kappa type. Immunofluorescent analysis of kidney biopsy showed extensive IgM and light kappa chain deposits, which caused membranoproliferative glomerulonephritis. Treatment with cyclophosphamide was ineffective and patient died 2 months later. The second patient is a 42-year-old female diagnosed with lymphoplasmacytic lymphoma and paraprotein IgG lambda type. The course of the disease was fulminant with developing nephrotic syndrome and fatal acute renal failure. Immunofluorescent and light microscopic studies of kidney biopsy showed signs of immunotactoid glomerulonephritis with deposits of IgG and C3. Hemodyalises and cytostatic therapy were without response and she died after 45 days.
报告了两名淋巴浆细胞淋巴瘤患者,其中一名患者存在IgM单克隆蛋白,另一名患者存在IgG和λ轻链,二者均患有肾病综合征和急性肾衰竭。一名58岁男性曾接受前B急性淋巴细胞白血病治疗,3年后因淋巴浆细胞淋巴瘤和高副蛋白IgM κ型并发症发展为肾病综合征。肾脏活检的免疫荧光分析显示广泛的IgM和κ轻链沉积,导致膜增生性肾小球肾炎。环磷酰胺治疗无效,患者2个月后死亡。第二名患者是一名42岁女性,诊断为淋巴浆细胞淋巴瘤和副蛋白IgG λ型。疾病过程迅猛,发展为肾病综合征和致命的急性肾衰竭。肾脏活检的免疫荧光和光镜研究显示免疫触须样肾小球肾炎的迹象,伴有IgG和C3沉积。血液透析和细胞抑制疗法均无反应,她在45天后死亡。