Prasad Bhanu, Tangedal Kirsten, Chibbar Rajni, McIsaac Mark
Department of Nephrology, Regina General Hospital, Regina, CAN.
Department of Pharmacology, Regina General Hospital, Regina, CAN.
Cureus. 2018 May 6;10(5):e2585. doi: 10.7759/cureus.2585.
A 77-year-old female was admitted to the hospital for an evaluation of congestive heart failure. She gave a history of progressive peripheral edema over eight to 10 months, extending up to the knees bilaterally. Admitting creatinine was 148 mmol/L, serum albumin was 15g/L, and urine protein on quantification was 9.09 g/day. Her immunoglobulin G (IgG) level was 18.4g/L and serum-free kappa level was 92.3 mg/L. The immunofixation of urine revealed monoclonal IgG kappa (1.97 g/d). Her kidney biopsy subsequently confirmed the diagnosis of immunoglobulin light chain (AL) amyloidosis. During the course of investigations, it was incidentally noted that she had a mass on her right kidney, which on biopsy was identified as renal cell carcinoma (RCC). This case deals with the rare situation of AL amyloidosis existing with a solid organ carcinoma and the therapeutic dilemma of treating two unrelated conditions involving the kidneys.
一名77岁女性因充血性心力衰竭入院评估。她有8至10个月进行性外周水肿病史,双侧水肿延伸至膝盖。入院时肌酐为148 mmol/L,血清白蛋白为15g/L,尿蛋白定量为9.09 g/天。她的免疫球蛋白G(IgG)水平为18.4g/L,血清游离κ轻链水平为92.3 mg/L。尿液免疫固定显示单克隆IgG κ(1.97 g/d)。随后她的肾脏活检确诊为免疫球蛋白轻链(AL)淀粉样变性。在检查过程中,偶然发现她右肾有一个肿块,活检确定为肾细胞癌(RCC)。本病例涉及AL淀粉样变性与实体器官癌并存的罕见情况以及治疗涉及双肾的两种不相关病症的治疗困境。