It is widely accepted that amyloidosis in Waldenstrom's macroglobulinemia (
WM) is exclusively due to amyloid light-chain deposition. However, only a s
mall number of previous reports have actually characterized the type of amy
loid in WM. We now report the third patient with WM and amyloid A protein (
AA) amyloidosis. This patient developed malabsorption, nephrotic syndrome,
and orthostatic hypotension. AA was immunohistochemically demonstrated in t
he rectal biopsy. In conjunction with previous examples of AA amyloidosis,
the present report raises the possibility that AA amyloidosis may also occu
r in WM patients. (C) 2001 The Japanese Society of Hematology.