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Case report: One case of primary AL amyloidosis repeatedly misdiagnosed as scleroderma

机译:病例报告:一例原发性AL淀粉样变性病反复被误诊为硬皮病

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摘要

Introduction: Amyloid light chain (AL) results from the deposition of immunoglobulin light chain fragments, and can affect multiple organs/systems. Our patient was diagnosed as scleroderma repeatedly because of extensive skin thickening and hardening, but the treatment was not effective. We did extensive laboratory examinations including serum/urine protein electrophoresis and flow cytometry assay of bone marrow aspiration. Conclusion: A diagnosis of primary AL amyloidosis was established.
机译:简介:淀粉样蛋白轻链(AL)来自免疫球蛋白轻链片段的沉积,可影响多个器官/系统。由于广泛的皮肤增厚和硬化,我们的患者被反复诊断为硬皮病,但治疗无效。我们进行了广泛的实验室检查,包括血清/尿蛋白电泳和骨髓穿刺的流式细胞仪检测。结论:诊断为原发性AL淀粉样变性。

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