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英语翻译
Immunoglobulin light chain(AL) amyloidosis is the most common acquired systemic amyloidoses.Its presentationis often insidious and progressive,which may delay diagnosis.The authors describea rare case of AL amyloidosis in a 34-year-old man with scleroderma-like manifestationsubstantiated by multifarious laboratory investigations and the histopathologicfeature of involved skin lesions stained with Congo red and crystal violet.Itwill help in maintaining a high clinical suspicion of the disease when confrontingthe similar skin presentation.
Immunoglobulin light chain(AL) amyloidosis is the most common acquired systemic amyloidoses.Its presentationis often insidious and progressive,which may delay diagnosis.The authors describea rare case of AL amyloidosis in a 34-year-old man with scleroderma-like manifestationsubstantiated by multifarious laboratory investigations and the histopathologicfeature of involved skin lesions stained with Congo red and crystal violet.Itwill help in maintaining a high clinical suspicion of the disease when confrontingthe similar skin presentation.
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