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Two Cases of Pelvic Diffuse Large B-Cell Lymphoma.
Rupam Sharma1, Arash Heidari1,2, Everardo Cobos1,2
1Kern Medical, Bakersfield, CA, USA.
Journal of Investigative Medicine High Impact Case Reports
|April 26, 2022
Summary
Primary pelvic lymphoma, a rare cancer, can mimic gynecological tumors. Early diagnosis of diffuse large B-cell lymphoma is crucial for effective treatment and improved patient outcomes.
Area of Science:
- Oncology
- Gynecologic Oncology
- Hematology
Background:
- Primary diffuse large B-cell lymphoma (DLBCL) of the pelvis is an uncommon extranodal presentation.
- This condition can be misdiagnosed as gynecological malignancy due to similar clinical presentations.
- Delayed diagnosis of DLBCL can negatively impact prognosis despite standardized curative treatments.
Purpose of the Study:
- To highlight the diagnostic challenges of extranodal pelvic DLBCL.
- To emphasize the importance of a multidisciplinary approach in managing these rare cases.
- To present case studies of patients initially suspected of gynecological malignancy but diagnosed with pelvic DLBCL.
Main Methods:
- Retrospective case review of two female patients.
- Clinical presentation analysis, including imaging and pathology.
- Review of diagnostic workup and treatment protocols.
Main Results:
- Both patients presented with pelvic masses, initially suspected as gynecological cancers.
- Final diagnosis confirmed diffuse large B-cell lymphoma of the pelvis in both cases.
- Patients were managed with appropriate lymphoma treatment protocols.
Conclusions:
- Extranodal pelvic DLBCL requires high clinical suspicion, especially when mimicking gynecological malignancies.
- A prompt and accurate diagnosis is essential for timely initiation of curative therapy.
- Multidisciplinary collaboration is key for optimal management of rare pelvic lymphomas.
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