The amyloidoses are biochemically heterogeneous diseases with pathophysiolo
gic deposits of various proteins. The clinical course, prognosis, and thera
py are different for each type of amyloidosis and, therefore, a type-specif
ic diagnosis is demanded as early as possible. We describe a method for typ
ing the most common systemic amyloidoses of AL, AA, and transthyretin types
by enzyme-linked immunosorbent assay (ELISA), using abdominal wall subcuta
neous fat biopsy specimens. The method was tested on 21 abdominal fat biops
y specimens that were sent to the laboratory. Of these, 15 contained amyloi
d that was successfully characterized in 14 cases. One specimen contained a
myloid that did not react with any antisera used. The 6 specimens without a
myloid gave no reaction in ELISA. The described ELISA method is reliable an
d easy to perform, and the tissue sample needed is obtained by minor surger
y.