Mantle cell lymphoma (MCL) is a subtype of non-Hodgkin lymphoma characterized by the proliferation of B-cells. Severe hyperleukocytosis is an uncommon presentation that can complicate the diagnosis and management of MCL. We present the case of an 80-year-old male patient suffering from MCL, who exhibited symptoms including severe hyperleukocytosis, lymphadenopathy, and significant bone marrow infiltration. Diagnostic procedures included complete blood count, bone marrow biopsy, lymph node needle biopsy, and flow cytometry to confirm the diagnosis. The patient exhibited a leukocyte count exceeding 491.28 x 109/L, 65.0% abnormal cell in peripheral blood, with bone marrow analysis revealing over 90% infiltration by mature B-cells. Immunohistochemical results of lymph node biopsy were considered for CyclinD1 (+) mantle cell lymphoma. This case highlights the need for careful differential diagnosis between MCL and other lymphoblastic leukemias in patients presenting with severe hyperleukocytosis. Accurate identification is essential for appropriate management and treatment.
Lv et al. (Mon,) studied this question.