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Solitary monoclonal plasma cell tumor of bone or soft tissue
Diagnosis of solitary bone plasmacytoma (SBP) requires
Solitary lesion, biopsy showing plasma cells
Negative skeletal survey, negative MR spine, pelvis, proximal femora/humeri
Negative clonal cells in marrow aspirate
No anemia, hypercalcemia, or renal involvement suggesting systemic myeloma
Axial skeleton > extremities
Thoracic vertebral body most common site
Radiographs/CT
Lytic, multicystic-appearing lesion ± vertical dense striations
Pathologic compression fracture common
T1 hypointense, T2/STIR hyperintense marrow with low signal, curvilinear areas
Posterior elements involved in most cases
± associated soft tissue mass (paraspinous or epidural with draped-curtain sign)
SBP may reflect early (stage I) multiple myeloma
SBPs considered clinical stage I Durie-Salmon lesions
Most common symptom = pain due to bone destruction
Epidural extension may cause compression of cord or nerve root
Mean age = 55 years (younger than age of patients with multiple myeloma)
Must exclude 2nd unanticipated lesion (33% of cases)
Solitary bone plasmacytoma (SBP), solitary myeloma, solitary plasma cell tumor
Solitary monoclonal plasma cell tumor of bone or soft tissue, without evidence of multiple myeloma (MM)
Diagnosis requires
Solitary lesion, biopsy showing plasma cells
Negative skeletal survey, negative MR spine, pelvis, proximal femora/humeri
Negative clonal cells in marrow aspirate
No anemia, hypercalcemia, or renal involvement suggesting systemic myeloma
Best diagnostic clue
T1 hypointense marrow with curvilinear hypointensities
Location
Axial skeleton most common site of involvement (25-60%), followed by extremities
Vertebral body = most common site of SBP
Thoracic > lumbar > cervical
Radiography
Can be normal early
Lytic, multicystic-appearing lesion ± vertical dense striations
Pathologic compression fracture common
No periosteal reaction
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