AL amyloidosis
From BugSigDB
AL Amyloidosis is a plasma cell disorder characterized by the aggregation and deposition of insoluble amyloid fibrils derived from misfolding of monoclonal immunoglobulin light chains usually produced by a plasma cell tumor (see this term). It usually presents as primary systemic amyloidosis (PSA) with multiple organ involvement and less frequently as primary localized amyloidosis (PLA; see these terms) restricted to a single organ.
- Aliases
- AL amyloidosis
- amyloidosis AL
- amyloidosis primary systemic
- Immunoglobulinic amyloidosis
- Light chain amyloidosis
- Light-chain amyloidosis
- primary AL amyloidosis
- Primary amyloidosis
- primary amyloidosis
- primary amyloidosis (formerly)
- primary systemic AL amyloidosis
- primary systemic amyloidosis
- systemic AL amyloidosis
- systemic AL amyloidsis
- Systemic monoclonal immunoglobulin light chain amyloidosis
