Systemic AL Amyloidosis: Current Approaches to Diagnosis and Management
Abstract. AL amyloidosis is characterized by a low-level expansion of an indolent, small plasma cell clone that produces amyloidogenic light chains. Amyloid aggregates or preceding intermediaries cause direct cell damage through their proteotoxicity, and amyloid deposits distort tissue architecture,...
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| Главные авторы: | , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Wiley
2020-08-01
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| Серии: | HemaSphere |
| Online-ссылка: | http://journals.lww.com/10.1097/HS9.0000000000000454 |
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