Miyazaki Daigo, Yazaki Masahide, Ishii Wataru, Matsuda Masayuki, Hoshii Yoshinobu, Nara Kenji, Nakayama Jun, Ikeda Shu-ichi
Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Japan.
Intern Med. 2011;50(3):243-6. doi: 10.2169/internalmedicine.50.4094. Epub 2011 Feb 1.
A 60-year-old woman was found to have proteinuria and a lung nodule. The surgically resected left upper lobe contained a nodule, in which the adenocarcinoma was surrounded by a heavy deposition of amyloid. Subsequent renal and gastric biopsies demonstrated amyloid deposition with Aλ immunoreactivity. She was treated with 2 courses of VAD (vincristine, doxorubicin and dexamethasone), resulting in the disappearance of Bence Jones proteinuria. Her nephrotic syndrome has been improving during the subsequent 3 years. The rare lung nodule consisting of adenocarcinoma and amyloid deposition was a diagnostic clue in this primary systemic AL amyloidosis patient.
一名60岁女性被发现有蛋白尿和肺部结节。手术切除的左上叶有一个结节,其中腺癌被大量淀粉样蛋白沉积所包围。随后的肾脏和胃活检显示淀粉样蛋白沉积伴Aλ免疫反应性。她接受了2个疗程的VAD(长春新碱、阿霉素和地塞米松)治疗,本-周蛋白尿消失。在随后的3年里,她的肾病综合征一直在改善。这个由腺癌和淀粉样蛋白沉积组成的罕见肺部结节是这位原发性系统性AL淀粉样变性患者的诊断线索。