A surgical case of solitary plasmacytoma of rib origin with biclonal gammopathy

Citation
M. Kadokura et al., A surgical case of solitary plasmacytoma of rib origin with biclonal gammopathy, JPN J CLIN, 30(4), 2000, pp. 191-195
Citations number
13
Categorie Soggetti
Oncology
Journal title
JAPANESE JOURNAL OF CLINICAL ONCOLOGY
ISSN journal
03682811 → ACNP
Volume
30
Issue
4
Year of publication
2000
Pages
191 - 195
Database
ISI
SICI code
0368-2811(200004)30:4<191:ASCOSP>2.0.ZU;2-4
Abstract
Localized solitary plasmacytoma of the bone (SPB) is a rare disease and is characterized by only one or two isolated bone lesions with no evidence of disease dissemination. A previously healthy 44-year-old male was admitted f or evaluation of an abnormal radiographic shadow in the left middle lung fi eld with symptoms of left back pain. Radiological evaluation revealed a per ipheral opacity in the left chest wall, which was highly suspected to be a chest wall tumor. CT-guided transcutaneous needle biopsy of the tumor was p erformed and the specimens showed a monomorphous population of mature plasm a cells. The bone marrow biopsy findings revealed no evidence of myeloma an d bone scanning revealed only abnormal accumulation in the left seventh rib . He had mild M-proteins in a urine sample and Bence-Jones protein was dete cted. Immunoelectrophoresis revealed mild biclonal gammopathy of Bence-Jone s protein of both the kappa and lambda light-chain types. Under a diagnosis of solitary bone plasmacytoma, preoperative radiation therapy with doses o f 40 Gy for the tumor was performed. He underwent complete en bloc resectio n of the chest wall, including one-third of the left sixth and seventh ribs , the intercostal muscle and the parietal pleura. The protein abnormalities in the urine sample disappeared following surgical resection. Adjuvant che motherapy using melphalan and prednisolone was performed. He is doing well without evidence of tumor recurrence 2 years following his initial diagnosi s.