2007AmyloidRequires access

An overview of high-dose melphalan and stem cell transplantation in the treatment of AL amyloidosis

Vaishali Sanchorawala, David C. Seldin

Open publisher page 31 citations

Abstract

AL amyloidosis is the most common form of systemic amyloidosis and is associated with an underlying plasma cell dyscrasia. This review outlines an overview of high-dose intravenous melphalan and stem cell transplantation in the treatment of AL amyloidosis. An algorithm of our recommendations for the treatment of AL amyloidosis is also outlined.

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What this paper is about

AL amyloidosis is the most common form of systemic amyloidosis and is associated with an underlying plasma cell dyscrasia. This review outlines an overview of high-dose intravenous melphalan and stem cell transplantation in the treatment of AL amyloidosis. An algorithm of our recommendations for the treatment of AL amyloidosis is also outlined.

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OpenAlex reports 31 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

AL amyloidosis is the most common form of systemic amyloidosis and is associated with an underlying plasma cell dyscrasia. This review outlines an overview of high-dose intravenous melphalan and stem cell transplantation in the treatment of AL amyloidosis. An algorithm of our recommendations for the treatment of AL amyloidosis is also outlined.

Key concepts: Melphalan, Plasma cell dyscrasia, AL amyloidosis, Amyloidosis, Medicine, Dyscrasia, Autologous stem-cell transplantation, Transplantation

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An overview of high-dose melphalan and stem cell transplantation in the treatment of AL amyloidosis — Research Paper | ScholarLens