Results 61 to 70 of about 2,806 (137)

A 44-Year-Old Man with Waldenstrom Macroglobulinemia and Bilateral Maxillary Sinusitis

Acta Medica Indonesiana, 2017
Waldenstrom macroglobulinemia is a chronic, indolent, lymphoproliferative disorder, which is characterized by the presence of a high macroglobulin (IgM) level, elevated serum viscosity, and the presence of a lymphoplasmacytic infiltrate in the bone ...
Shinta Oktya Wardhani, Herman Bagus Trianto, Muhammad Anshory   +2 more
doaj   +2 more sources

Schnitzler Syndrome as an Autoinflammatory Disease Driven by B‐Cell‐Specific Somatic MYD88 Mutation

Allergy, EarlyView.
Yuyi Zhou, Yoko Ueki, Naoya Iwata, Hiroshi Oue, Kentaro Kato, Mengyan Li, Kazushi Izawa, Tomoyasu Jo, Seishi Ogawa, Kenji Kabashima, Naotomo Kambe   +10 more
wiley   +1 more source

Machine learning enhances risk stratification and treatment failure prediction in diffuse large B‐cell lymphoma

HemaSphere, Volume 10, Issue 4, April 2026.
Abstract Diffuse large B‐cell lymphoma (DLBCL) is the most common lymphoma subtype worldwide. Existing prognostic models, including the National Comprehensive Cancer Network International Prognostic Index (NCCN IPI), rely on small predefined variable sets, discretized inputs, and do not incorporate longitudinal clinical histories or nonlinear ...
Mikkel Werling, Alexander D. Fuglkjær, Peter Brown, Carsten U. Niemann, Rudi Agius   +4 more
wiley   +1 more source

Cutaneous primary B-cell lymphomas: from diagnosis to treatment [PDF]

, 2015
Primary cutaneous B-cell lymphomas are a heterogeneous group of mature B-cells neoplasms with tropism for the skin, whose biology and clinical course differ significantly from the equivalent nodal lymphomas.
Lima, M.
core   +3 more sources

Waldenström Macroglobulinemia: Unusual Presentation With Cast Nephropathy/Light Chain Tubulopathy

Clinical Medicine Insights: Case Reports, 2019
Cast Nephropathy/Light chain tubulopathy is usually present in patients with multiple myeloma and is very rare in patients with Waldenstrom Macroglobulinemia. There are very few case reports mentioned in the literature.
Muddasir Ashraf, Prerna Rastogi
doaj   +1 more source

Rare presentation of double-clonal Waldenström macroglobulinemia with pulmonary embolism: A case report

Open Life Sciences, 2023
Waldenström macroglobulinemia (WM) rarely leads to pulmonary embolism. Due to its low incidence, the underlying pathophysiology, prognosis, and optimal treatment remain largely unexplored and uninvestigated.
Sun Yan, Meng Fan-Jun, Huang Jun-Xia, Yan Xue-Shen, Zhao Xia, Zhou Jing-Jing, Gao Yan   +6 more
doaj   +1 more source

Fatal Non‐Hepatic Hyperammonemia Post‐Glofitamab: Ureaplasma and Genetic Susceptibility: A Case Report

Immunity, Inflammation and Disease, Volume 14, Issue 4, April 2026.
ABSTRACT Background Although primarily reported in solid organ transplant recipients and patients undergoing chimeric antigen receptor T‐cell immunotherapy (CAR‐T), non‐hepatic hyperammonemia (NHHA) is a rare but lethal complication in the broader context of post‐ chemo‐immunotherapy hematologic malignancies.
Yinshan Wu, Xiuliu Guo, Xiaoling Wang, Feng Guo   +3 more
wiley   +1 more source

STUDIES OF EPIGENETICS AND PROPERTIES OF B CELL RECEPTOR IN WALDENSTRÖM MACROGLOBULINEMIA (WM) [PDF]

, 2023
Waldenström macroglobulinemia (WM) is an indolent lymphoproliferative disorder with aberrant monoclonal immunoglobulin M (IgM) production that is associated with disease symptoms.
Karbalivand, Mona
core   +1 more source

Therapeutic targeting of MALT1 in oncology: Mechanism, inhibitor development, and clinical prospects

Journal of Cell Communication and Signaling, Volume 20, Issue 1, March 2026.
Abstract MALT1, a multifunctional protease molecule, plays a pivotal role in the adaptive immunity by regulating immune cell survival, proliferation and activation through the nuclear transcription factor‐κB (NF‐κB) signaling pathway by scaffold and protease activities.
Xintao Cao, Peixia Wang, Yuan Ji, Yongliang Sun, Dejiu Zhang   +4 more
wiley   +1 more source

Zanubrutinib for high-risk Waldenström macroglobulinemia with complex karyotype and hyperleukocytosis: A case report and literature review

SAGE Open Medical Case Reports
To report the management and outcome of an elderly, high-risk lymphoplasmacytic lymphoma/Waldenström macroglobulinemia patient presenting with severe symptomatic anemia, marked hyperleukocytosis, a complex karyotype, dual MYD88/CXCR4 mutations, and ...
Jiale Chen, Jieyi Zhou, Chengyang Xu, Bo Zheng, Jie He, Rong Li   +5 more
doaj   +1 more source