Results 31 to 40 of about 7,257 (109)

Differential Diagnosis of Waldenström’s Macroglobulinemia and Early Management: Perspectives from Clinical Practice

open access: yesBlood and Lymphatic Cancer: Targets and Therapy, 2022
Shashank Cingam,1 Surbhi Sidana2 1Division of Hematology and Oncology, University of New Mexico Comprehensive Cancer Center, Albuquerque, NM, 87102, USA; 2Division of BMT and Cell Therapy, Stanford University School of Medicine, Stanford, CA, 94305 ...
Cingam S, Sidana S
doaj  

Severe nephritis as initial sign of Waldenström’s macroglobulinemia

open access: yesClinics and Practice, 2019
Waldenström’s macroglobulinemia (WM), characterized with monoclonal immunoglobulins of type M and lymphoplasmacytic lymphoma, is a rare clonal Bcell disorder.
Thomas Knoop   +5 more
doaj   +1 more source

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

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   +1 more source

New developments in the management of Waldenström macroglobulinemia

open access: yesCancer Management and Research, 2017
Jithma P Abeykoon,1 Uday Yanamandra,2 Prashant Kapoor1,3 1Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA; 2Department of Hematology and Stem Cell Transplant, Army Hospital (Research & Referral), Delhi, India; 3Division of Hematology,
Abeykoon JP, Yanamandra U, Kapoor P
doaj  

Primary cold agglutinin-associated lymphoproliferative disease: a B-cell lymphoma of the bone marrow distinct from lymphoplasmacytic lymphoma

open access: yesHaematologica, 2014
Primary chronic cold agglutinin disease is a rare hemolytic disease mediated by monoclonal IGHV4-34-encoded cold agglutinins with a predominant specificity for the blood group antigen I.
Ulla Randen   +8 more
doaj   +1 more source

CD19-negative non-IgM type lymphoplasmacytic lymphoma: a case report and literature review

open access: yesFrontiers in Oncology
Lymphoplasmacytic lymphoma (LPL) that does not fulfill the diagnostic criteria for Waldenström’s macroglobulinemia (WM), termed non-IgM type LPL, represents a rare entity that poses significant diagnostic challenges.
Feng Lu   +11 more
doaj   +1 more source

Lymphoplasmacytic lymphoma associated with diffuse large B-cell lymphoma: Progression or divergent evolution?

open access: yesPLoS ONE, 2020
AimLymphoplasmacytic lymphoma (LPL) is an indolent mature B-cell-neoplasm with involvement of the bone marrow. At least 90% of LPLs carry MYD88-L265P mutation and some of them (~10%) transform into diffuse large B-cell-lymphoma (DLBCL).Material and ...
Macarena Boiza-Sánchez   +13 more
doaj   +1 more source

Acute liver injury in the course of lymphoplasmacytic lymphoma

open access: yesCurrent Issues in Pharmacy and Medical Sciences, 2019
Non-Hodgkin lymphomas are malignant neoplasms whose incidence rates increase each year. These also include neoplasms rare in the general population. The present case report described a patient with lymphoplasmacytic lymphoma (LPL) and rapid liver damage.
Dorota Kuzemko-Baranowska   +2 more
doaj   +1 more source

Short colon syndrome in cats

open access: yesJournal of Veterinary Internal Medicine
Background Shortening of the colon has been described in cats, but its imaging and clinicopathological features remain poorly understood. Objectives Description of the signalment, clinical presentation, imaging, endoscopic and histological features of ...
Audrey P. King   +4 more
doaj   +1 more source

Response to ibrutinib of a refractory IgA lymphoplasmacytic lymphoma carrying the MYD88 L265P gene mutation

open access: yesMediterranean Journal of Hematology and Infectious Diseases, 2019
In 2014 a 66 year-old woman presented with anemia and an IgAk monoclonal spike. Bone marrow (BM) biopsy showed 80% lymphocytes and lymphoplasmacytoid cells. Computed Tomography (CT) scan documented neither adenopathy nor splenomegaly.
Francesca Maria Quaglia   +9 more
doaj   +1 more source

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