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Published on: March 25, 2022
A Patient with Synchronous Gallbladder and Bone Plasmacytoma.
Mariam Markouli1, Alexia Saridaki2, Nora-Athina Viniou1
1First Department of Internal Medicine, Laikon General Hospital, National and Kapodistrian University of Athens, 11527 Athens, Greece.
This report details a rare case of plasmablastic extramedullary plasmacytoma in the gallbladder, unexpectedly diagnosed via imaging. The study highlights diagnostic and management challenges for this rare plasma cell tumor.
Area of Science:
- Oncology
- Pathology
Background:
- Multiple myeloma (MM) is a common bone tumor; extramedullary plasmacytoma (EMP) is rare, typically in the head/neck.
- Gastrointestinal and gallbladder EMP are exceedingly rare, often mimicking gallstone disease.
Purpose of the Study:
- To present a rare case of plasmablastic extramedullary plasmacytoma (PE-EMP) of the gallbladder.
- To discuss the diagnostic, therapeutic, and prognostic challenges associated with EMPs, particularly the plasmablastic subtype.
Main Methods:
- Case report of a 61-year-old asymptomatic patient diagnosed with gallbladder EMP.
- Utilized abdominal ultrasound (US), magnetic resonance imaging (MRI), and fluorodeoxyglucose positron emission computed tomography (FDG PET-CT).
Main Results:
- Unexpectedly diagnosed PE-EMP in the gallbladder of an asymptomatic patient.
- Concurrent bone plasmacytoma identified in the femur.
- Patient is undergoing chemotherapy and preparation for autologous stem cell transplantation.
Conclusions:
- PE-EMP presents unique diagnostic and management challenges.
- Distinguishing plasmablastic subtype from other EMPs is crucial for effective treatment.
- Early detection and tailored therapy are key for improving outcomes in rare plasma cell neoplasms.
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