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Atypical thoracic solitary plasmacytoma
Dong Hwan Kim1, Seung Don Yoo, Sung Min Kim
1Department of Physical Medicine and Rehabilitation, College of Medicine, Kyung Hee University, Seoul 130-702, Korea.
Annals of Rehabilitation Medicine
|November 28, 2012
Summary
A rare spinal tumor, solitary plasmacytoma, caused chest pain, weakness, and allesthesia in a 54-year-old man. Surgical removal led to complete symptom resolution, highlighting effective treatment for this bone neoplasm.
Area of Science:
- Oncology
- Neurology
- Orthopedics
Background:
- Plasmacytoma is a rare plasma cell neoplasm, with solitary bone plasmacytoma accounting for 5% of cases.
- Solitary bone plasmacytoma predominantly affects the axial skeleton, particularly thoracic vertebrae, due to red marrow presence.
- The condition affects 2-3 individuals per 100,000 population.
Purpose of the Study:
- To report a unique case of solitary plasmacytoma of the spine.
- To illustrate the diagnostic challenges and successful treatment of spinal plasmacytoma.
- To highlight the potential for neurological recovery after surgical intervention.
Main Methods:
- Case report of a 54-year-old male presenting with chest pain, weakness, and allesthesia.
- Magnetic Resonance Imaging (MRI) revealed a mass lesion in the T5 vertebra.
- Surgical intervention followed by biopsy confirmed solitary plasmacytoma of the spine.
Main Results:
- The patient presented with atypical symptoms including chest pain, weakness, and allesthesia.
- Initial laboratory findings were unremarkable, complicating diagnosis.
- Post-operative biopsy confirmed solitary plasmacytoma of the spine.
- The patient experienced complete resolution of weakness and allesthesia 5 months after surgery.
Conclusions:
- Solitary plasmacytoma of the spine can present with diverse neurological symptoms.
- Early surgical intervention is crucial for managing spinal plasmacytoma and associated neurological deficits.
- Complete recovery is achievable following surgical resection of solitary spinal plasmacytoma.
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