<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(1)</volume><submitter>Seijari MN</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Primary splenic lymphoma is a rare lymphoproliferative disorder that involves the spleen, exhibits diverse clinical presentations, and lacks a clear consensus in terms of management strategies.&lt;h4>Case presentation&lt;/h4>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 rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone [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.&lt;h4>Conclusion&lt;/h4>Remarkably, despite using a shortened course of R-CHOP, the patient achieved complete resolution, and a positron emission tomography scan conducted at the end of the 6-month posttreatment period confirmed sustained complete remission.</pubmed_abstract><journal>Case reports in oncology</journal><pagination>447-453</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10919911</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Primary Splenic Diffuse Large B-Cell Lymphoma: A Case Report and Literature Review of a Rare Condition.</pubmed_title><pmcid>PMC10919911</pmcid><pubmed_authors>Seijari MN</pubmed_authors><pubmed_authors>Elfaieg A</pubmed_authors><pubmed_authors>Elkourashy SA</pubmed_authors><pubmed_authors>Kaspo S</pubmed_authors><pubmed_authors>Alshurafa A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Primary Splenic Diffuse Large B-Cell Lymphoma: A Case Report and Literature Review of a Rare Condition.</name><description>&lt;h4>Introduction&lt;/h4>Primary splenic lymphoma is a rare lymphoproliferative disorder that involves the spleen, exhibits diverse clinical presentations, and lacks a clear consensus in terms of management strategies.&lt;h4>Case presentation&lt;/h4>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 rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone [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.&lt;h4>Conclusion&lt;/h4>Remarkably, despite using a shortened course of R-CHOP, the patient achieved complete resolution, and a positron emission tomography scan conducted at the end of the 6-month posttreatment period confirmed sustained complete remission.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan-Dec</publication><modification>2025-04-04T12:34:50.186Z</modification><creation>2025-04-04T12:34:50.186Z</creation></dates><accession>S-EPMC10919911</accession><cross_references><pubmed>38455716</pubmed><doi>10.1159/000537780</doi></cross_references></HashMap>