Primarysplenic Large Cell B Lymphoma: Case Report
Khadija Bellahammou, Narimane Salmi, Hamza Ettahri, Mustapha El Kabous, MeryemAit lhaj, Sihame Lkhoyaali, Hind Mrabti, Hassan Errihani
Affiliation
Department of Medical Oncology, National Institute of Oncology, Rabat, Morocco
Corresponding Author
Asmaa Lakhdissi, Department of Medical Oncology, National Institute of Oncology, Rabat, Morocco, E-mail: asmaalakhdissi@gmail.com
Citation
Lakhdissi, A,. et. al. Primarysplenic Large Cell B Lymphoma: Case Report. (2016) J Gastro Dis Liver Func 2(2): 73- 76.
Copy rights
© 2016 Lakhdissi, A. This is an Open access article distributed under the terms of Creative Commons Attribution 4.0 International License.
Keywords
Abstract
Background: Primary splenic lymphoma is a rare disease with heterogeneous definition, compromising less than 1% of non-Hodgkin’s lymphoma.
Case presentation: We are reporting a case of 50 year old man who presented splenomegaly, fever, weight loss and night sweats. The investigations revealed a splenomegaly with splenic lesion which cancorrespond to abscess. The patient underwent splenectomy for definitive diagnosis and treatment. Diagnosis of primary diffuse large B cell lymphoma of the spleen was made and confirmed by immunochemistry and the patient received 6 cycles of RCHOP (Rituximab + cyclophosphamide + Adriamycin + vincristine + prednisone) and he is currently well and in complete remission more than 1 year after diagnosis.
Conclusion: Primary splenic lymphoma is rare; splenectomy is an important step in its diagnosis and treatment. Early splenectomy combined with chemotherapy is an optimal strategy.