苯达莫司汀
美罗华
免疫球蛋白M
淀粉样变性
医学
免疫球蛋白轻链
抗体
免疫学
免疫球蛋白G
病理
作者
Richa Manwani,Sajitha Sachchithanantham,Shameem Mahmood,Darren Foard,Faye Sharpley,Tamer Rezk,Thirusha Lane,Cristina Quarta,Marianna Fontana,Helen J. Lachmann,Julian D. Gillmore,Carol Whelan,Philip N. Hawkins,Ashutosh Wechalekar
出处
期刊：Blood
[Elsevier BV]
日期：2018-06-20
卷期号：132 (7): 761-764
被引量：31
标识
DOI：10.1182/blood-2018-04-846493
摘要
TO THE EDITOR:
Systemic amyloid light-chain amyloidosis (AL) is characterized by deposition of misfolded immunoglobulin light chains within organs. AL with an immunoglobulin M (IgM) monoclonal protein (IgM-AL) accounts for 5% to 7% of AL and exhibits more prevalent lymph node, neuropathic, and lung
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