Table of Contents
Definition / general | Epidemiology | Sites | Clinical features | Diagnosis | Laboratory | Radiology description | Radiology images | Prognostic factors | Case reports | Treatment | Clinical images | Microscopic (histologic) description | Microscopic (histologic) images | Differential diagnosisCite this page: Solitary plasmacytoma. PathologyOutlines.com website. http://www.pathologyoutlines.com/topic/bonesolitaryplasmacytoma.html. Accessed July 14th, 2017.
Definition / general
- Defined by WHO 2008 as a localized bone tumor consisting of monoclonal plasma cells, with no other bone lesions, no bone marrow involvement and no clinical features of myelomas
Epidemiology
- Rare; < 5% of myeloma patients
- Majority are males
- Median age is 50 - 55 years
Sites
- Sites of active bone marrow hematopoiesis
- 40% - 60% in axial spine; also vertebrae, thoracic more than lumbar and cervical
- Followed by ribs, skull, pelvis, femur, clavicle, scapula
- Long bone involvement below elbow and knee are rare
- Rarely involves lymph nodes or peripheral blood
Clinical features
- Incidental finding
- May have bone pain and pathologic fracture
- May cause soft tissue mass
Diagnosis
- Diagnostic criteria:
- Single bony lesion consisting of monoclonal plasma cells; MRI may be needed to exclude involvement of other sites
- No bone marrow involvement
- No clinical features of myeloma, such as anemia, hypercalcemia and renal failure
- Absence or low levels of M protein in urine
- Normal levels of uninvolved polyclonal immunoglobulins (Br J Haematol 2004;124:717)
Laboratory
- CBC, renal function tests, serum calcium (to exclude myeloma)
- Immunofixation studies in serum and urine (M protein detection)
Radiology description
- Osteolytic lesions, similar to myeloma
- May show soft tissue extension
- Vertebral involvement may be associated with spinal cord or nerve root compression
Radiology images
Prognostic factors
- Median survival is 10 years
- 50% eventually develop myeloma, 1 / 3 remain disease free > 10 years after radiotherapy
- Poor prognostic factors are large size and M protein persistence after radiotherapy
Case reports
- 36 year old man with anaplastic tumor (Arch Pathol Lab Med 2004;128:237)
- 43 year old woman with solitary bone plasmacytoma of lumbar spine (Eur Spine J 2014;23:35)
- 52 year old patient with maxillary solitary recurrent plasmacytoma (Chirurgia (Bucur) 2013;108:732)
- 64 year old woman with solitary bone plasmacytoma (Can Respir J 2013;20:11)
- Extended resection of a plasmocytoma of bone and an amyloidoma of the chest wall (Ann Thorac Surg 2013;96:2223)
- Solitary plasmacytoma of the medial clavicle (Am J Orthop (Belle Mead NJ) 2013;42:230)
Treatment
- Local control by radiotherapy is curative for most cases
Microscopic (histologic) description
- Similar to myeloma, easily diagnosed unless plasmablastic or anaplastic
- Cytologic, immunophenotypic and molecular features are similar to myeloma
Microscopic (histologic) images
Differential diagnosis









