The World Health Organization (WHO) and the International Consensus Classification (ICC) categorize these into three main entities:
Strong association with autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic purpura (ITP). 5. Management and Treatment Download Lymphomes splГ©niques pdf
Splenic Lymphomas: Pathophysiological Characteristics, Diagnosis, and Management The World Health Organization (WHO) and the International
Search for "Splenic Marginal Zone Lymphoma guidelines." diagnostic criteria (histology and immunophenotype)
Splenic lymphomas represent a heterogeneous group of rare B-cell neoplasms primarily involving the spleen, bone marrow, and often the peripheral blood. The most common subtype is Splenic Marginal Zone Lymphoma (SMZL). This paper reviews the clinical presentation, diagnostic criteria (histology and immunophenotype), and evolving therapeutic strategies for these malignancies. 1. Introduction
Now reserved for refractory cases or emergency management of splenic rupture.