Primary Splenic Diffuse Large B Cell Lymphoma A case report and literature review of a rare condition

Author:

Seijari Mohammed Najdat1,Kaspo Samer1,Alshurafa Awni2,Elfaieg Amro2,Elkourashy Sarah A.3

Affiliation:

1. Hamad General Hospital, Hamad Medical Corporation

2. Hamad Medical Corporation

3. Weill Cornell Medical College

Abstract

Abstract Primary splenic lymphoma represents a rare lymphoproliferative disorder that involves the spleen, exhibiting diverse clinical presentations and lacking a clear consensus in terms of management strategies. We present the case of a 52-year-old patient with a complex medical history, marked by multiple chronic medical conditions. The patient was diagnosed with primary splenic lymphoma, specifically the diffuse large B-cell subtype. Treatment for our patient involved a shortened course of chemotherapy (4 cycles of R-CHOP followed by two doses of rituximab) due to issues related to compliance and treatment-related complications. This was followed by consolidative radiotherapy, without resorting to splenectomy. Remarkably, the patient achieved complete resolution, and a positron emission tomography (PET) scan conducted at the end of the 6-month post-treatment period confirmed sustained complete remission.

Publisher

Research Square Platform LLC

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4. Splenomegaly in 2,505 patients in a large university medical center from 1913 to 1995. 1913 to 1962: 2,056 patients;O'Reilly RA;Western J Med,1998

5. Azar RK, Al-Hawary S, M. M., Francis IR (2010) Primary and secondary neoplasms of the spleen. Cancer imaging: the official publication of the International Cancer Imaging Society, 10(1), 173–182. https://doi.org/10.1102/1470-7330.2010.0026

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