AI Article Synopsis

  • Recurrence of multiple myeloma after autologous stem cell transplantation is a significant challenge for patients, with rare cases involving pleural manifestations following chemotherapy.
  • A 48-year-old man presented with symptoms like cough and fever, experiencing pleural effusion due to a relapse of his disease a year post-transplant, without bone marrow involvement.
  • Treatment involved a combination of medications, including dexamethasone and thalidomide, which were effective and showed no major side effects, highlighting the need for awareness of unusual relapse presentations in multiple myeloma patients.

Article Abstract

Background: Recurrence of multiple myeloma is among the most challenging issues for patients and treating physicians reported after autologous stem cell transplantation. However, extramedullary involvement after chemotherapy and transplantation has been rarely reported, especially as pleural manifestations. Protein electrophoresis indicated immunoglobulin A monoclonal kappa plasma cell neoplasm in our case.

Case Presentation: A 48-year-old middle-eastern man was referred to our clinic with cough, dyspnea, fever, and left side pleural effusion. A year after chemotherapy and autologous bone marrow transplantation, the patient presented with features in favor of pleural relapse, without bone marrow involvement. Protein electrophoresis demonstrated immunoglobulin A monoclonal kappa plasma cell neoplasm in our case. The patient was effectively treated with dexamethasone, thalidomide, cisplatin, doxorubicin, cyclophosphamide, and etoposide with no notable adverse effects.

Conclusion: Physicians should be aware of various presentations of multiple myeloma relapse, especially in autologous stem cell transplantation patients. Atypical and unique presentations such as the pleural involvement warrant further reporting of evidence to provide early management and treatment options.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9912644PMC
http://dx.doi.org/10.1186/s13256-023-03765-9DOI Listing

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