Amyloidosis

被引:110
作者
Gertz, MA [1 ]
Lacy, MQ
Dispenzieri, A
机构
[1] Mayo Clin & Mayo Fdn, Div Hematol & Internal Med, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Grad Sch Med, Rochester, MN 55901 USA
关键词
D O I
10.1016/S0889-8588(05)70122-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Amyloidosis is considered rare but has an incidence similar to that of Hodgkin's disease and chronic granulocytic leukemia. The diagnosis should be considered in any patient with unexplained nephrotic-range proteinuria, heart failure, peripheral neruopathy, or hepatomegaly. If a monoclonal protein is found in a patient with any of these clinical presentations, a biopsy should be performed and the specimen stained with Congo red. The simplest source of diagnostic material is subcutaneous fat tissue. Treatment usually consists of chemotherapy, which may be oral and low dose or high dose with stem cell rescue.
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页码:1211 / +
页数:24
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