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 ma
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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 ma
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.
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 ma
Cadeia leve de imunoglobulina (AL) amiloidose é o amyloidoses sistêmicas adquiridas mais comuns.Seus presentationis muitas vezes insidioso e progressivo,o que pode atrasar o diagnóstico.Os autores describea caso raro de amiloidose AL em um homem de 34 anos de idade,com esclerodermia-like manifestationsubstantiated por exames laboratoriais variadas ea histopathologicfeature de lesões de pele envolvidos corados com Congo vermelho violeta e cristal.Itwill ajudar na manutenção de uma elevada suspeita clínica da doença quando confrontingthe apresentação semelhante pele.