目的：探讨原发性系统性淀粉样变性并发凝血因子x缺乏的临床特征、发病机制及治疗方法。
Objective: to investigate the clinical feature, pathogenesis, and therapy of Primary systemic amyloidosis with acquired factor-X deficiency.
原发性肾淀粉样变性11例，继发性肾淀粉样变性4例。
Primary kidney amyloidosis was found in 11 cases, and secondary kidney amyloidosis in 4 cases.
原发性肾淀粉样变性11例，继发性肾淀粉样变性4例。
Primary kidney amyloidosis was found in 11 cases, and secondary kidney amyloidosis in 4 cases.
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