Primary localized amyloidosis

Primary localized amyloidosis is a form of AL amyloidosis caused by the aggregation of insoluble amyloid fibrils derived from misfolded monoclonal immunoglobulin light chains usually produced by a plasma cell tumor and characterized by localized amyloid deposition with clinical manifestations restricted to the organ involved, most frequently urinary tract (bladder), eye, respiratory tract (larynx, lungs), and skin.

Also known as: localised AL amyloidosis, localized AL amyloidosis

11 clinical trials for this condition and its sub-types, 0 tagged with Primary localized amyloidosis itself.