Amyloidosis is a rare systemic disease caused by extracellular deposition of insoluble protein. Systemicamyloidosis is subclassified into idiopathic primary and secondary form. The cause of secondary amyloidosisincludes tuberculosis, familial Mediterranean fever, rheumatoid arthritis and multiple myeloma. We report a caseof tuberculosis-related, secondary systemic amyloidosis which involves liver, spleen, kidneys, stomach, urinarybladder and lymph nodes.