Dee C H, Missirian R J, Chernoff I J
Division of Orthopaedic Surgery, Southern Illinois University, Springfield, USA.
Spine (Phila Pa 1976). 1998 Feb 15;23(4):497-500. doi: 10.1097/00007632-199802150-00019.
A rare case is reported of primary or idiopathic amyloidoma of the spine derived from production of light chain immunoglobulins. The tumor was successfully treated by anterior decompression and fusion with a fibula strut allograft.
To describe a rare case of AL amyloidoma of the spine.
Radiographic characteristics of this benign deposit are similar to harmful aggressive conditions afflicting the spine.
The patient returned to full function after the surgery with no evidence of systemic amyloidosis or development of multiple myeloma.
An isolated AL amyloidoma of the spine was resected and successfully reconstructed with a fibula strut allograft and internal fixation.
Isolated deposits of amyloid in the spine occur very rarely. When no evidence of myeloproliferative disease or systemic amyloidosis is found, prognosis is excellent. The deposit, when it occurs in the spine has a predilection for the thoracic region and can cause neurologic compromise, pain, and deformity that is responsive to decompression and fusion. The diagnosis of primary amyloidoma requires histologic studies for confirmation.
