Results 11 to 20 of about 4,273 (136)

Prognostic value of MYD88/CXCR4 mutation allele fraction in Waldenström macroglobulinemia using a multiplex ddPCR assay [PDF]

open access: yesHemasphere
HemaSphere, Volume 10, Issue 6, June 2026.
Eleni Thanou   +18 more
wiley   +2 more sources

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

open access: yesSAGE 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   +5 more
doaj   +2 more sources

Mixed cryoglobulinemia; a rare presentation of Waldenström macroglobulinemia [PDF]

open access: yesJournal of Nephropathology, 2022
Type II mixed cryoglobulinemia is a systemic disease mediated by immune complexes. Renal involvement is present in almost one third of the cases and the membranoprolifer-ative pattern is the most common histological presentation.
Catarina Isabel Ribeiro   +5 more
doaj   +1 more source

Bilateral central retinal vein occlusion as an initial presentation of Waldenström macroglobulinemia: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Waldenström macroglobulinemia is a rare hematological malignancy and is the most common diagnosis in patients with hyperviscosity syndrome.
Suraj Shrestha   +9 more
doaj   +1 more source

Ibrutinib effect in acquired von Willebrand syndrome secondary to Waldenström macroglobulinemia

open access: yesTherapeutic Advances in Hematology, 2021
The pathological increase of clonal IgM in Waldenström macroglobulinemia can be associated with acquired von Willebrand syndrome and can be a major risk of bleeding symptoms in this subgroup of patients with Waldenström macroglobulinemia.
María Poza   +6 more
doaj   +1 more source

A rare clinical presentation of Waldenström Macroglobulinemia mimicking lung cancer

open access: yesRespiratory Medicine Case Reports, 2022
Waldenström macroglobulinemia rarely presents as pulmonary symptoms, and even rarer as chylothorax. We present a patient who presented with bilateral pleural effusion and a 30 mm solid lesion in the lung.
Michael RT. Laursen   +4 more
doaj   +1 more source

Pattern of somatic mutations in patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significance

open access: yesHaematologica, 2017
We analyzed MYD88 and CXCR4 mutation status of 260 patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significance using allele-specific real time quantitative polymerase chain reaction and Sanger sequencing ...
Marzia Varettoni   +12 more
doaj   +1 more source

Multimodal Imaging of Waldenstrom Macroglobulinemia-Associated Hyperviscosity-Related Retinopathy Treated with Plasmapheresis

open access: yesCase Reports in Ophthalmological Medicine, 2021
While plasmapheresis is well known to significantly improve both retinal findings and systemic manifestations associated with Waldenstrom macroglobulinemia, few reports exist documenting changes in optical coherence tomography angiography (OCT-A).
Michael J. Schatz   +5 more
doaj   +1 more source

Waldenstrom macroglobulinemia involving the superior rectus muscle

open access: yesAmerican Journal of Ophthalmology Case Reports, 2018
Purpose: We present the first reported case of Waldenstrom macroglobulinemia in the right superior rectus causing diplopia. Observations: A 72-year-old man with a 6-month history of untreated asymptomatic Waldenstrom macroglobulinemia presented with 2 ...
J.B. Hellman, G.J. Harocopos, L.K. Lin
doaj   +1 more source

Bing-Neel syndrome, a rare complication of Waldenström macroglobulinemia: analysis of 44 cases and review of the literature. A study on behalf of the French Innovative Leukemia Organization (FILO).

open access: yesHaematologica, 2015
Central nervous system involvement by malignant cells is a rare complication of Waldenström macroglobulinemia, and this clinicopathological entity is referred to as the Bing-Neel syndrome.
Laurence Simon   +20 more
doaj   +1 more source

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