AI Article Synopsis

  • A rare case of spontaneous regression (SR) was observed in an elderly patient with multiple solitary plasmacytoma (MSP) who did not receive chemotherapy due to health concerns.
  • Despite initial worsening of the patient's condition, including new symptoms and bone lesion deterioration, all clinical issues disappeared by the 6-month mark, with complete metabolic remission confirmed after one year.
  • Findings indicated a possible role of the immune response and Epstein-Barr virus infection in the regression of the tumors, highlighting the need for more research to understand the mechanisms behind this phenomenon.

Article Abstract

We report a rare case of spontaneous regression (SR) in an elderly untreated patient with multiple solitary plasmacytoma (MSP). Diagnosis of MSP was confirmed through surgical resection of the left nasal cavity mass and subsequent biopsy of the right humerus. The patient was considered ineligible for chemotherapy due to poor performance status. At 3-month post-diagnosis, the patient's condition worsened with deteriorating bone lesions and emergence of a new serum monoclonal protein. However, these clinical findings completely disappeared at 6 months, and positron emission tomography-computed tomography at 1 year confirmed complete metabolic remission. Notably, peripheral blood lymphocyte counts were inversely correlated with tumor progression and remission. Pathological re-evaluation of the initial biopsy specimens revealed programmed cell death protein 1 (PD-1) expression in tumor-infiltrating CD8 T cells. In addition, tumor cells were infected with Epstein-Barr virus (EBV) but were negative for programmed cell death ligand 1 (PD-L1) expression, which is the most potent immune escape mechanism in tumor cells. While the mechanism underlying SR remains unclear, our findings suggest that host immune response as well as EBV infection may contribute to SR. Further studies are needed to elucidate the clinicopathologic mechanisms of tumor regression in plasma cell neoplasms.

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http://dx.doi.org/10.1007/s12185-024-03765-5DOI Listing

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