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

病例报告:一例原发性AL淀粉样变性反复误诊为硬皮病的病例

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Abstract

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.

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