Results 61 to 70 of about 403,362 (211)

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  

Primary cutaneous marginal zone lymphoma

open access: yesTurkish Journal of Plastic Surgery, 2021
We report the case of a histologically confirmed primary cutaneous marginal zone B-cell lymphoma (PCMZL), which was treated by surgical excision. PCMZL is the second-most common type of primary cutaneous lymphoma, including cells of the marginal zone ...
Ali Gokkaya   +3 more
doaj   +1 more source

Lymphoplasmacytic Lymphoma: A Case Report

open access: yesRGUHS Journal of Medical Sciences, 2022
Lymphoplasmacytic lymphoma LPL is a rare neoplasm composed of an admixture of small B lymphocytes lymphoplasmacytoid cells and plasma cells of the bone marrow lymph node and spleen. We report a case of a 65-year-old male who presented with diarrhea and hematochezia and the investigation revealed LPL.
J. Latha Fathima, Sitalakshmi S
openaire   +1 more source

Australian clinical practice guideline: diagnosis and treatment of idiopathic multicentric Castleman disease

open access: yesInternal Medicine Journal, EarlyView.
Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar   +16 more
wiley   +1 more source

ULK4 and CDKN2A polymorphisms influence the risk of developing monoclonal gammopathy of undetermined significance

open access: yesInternational Journal of Cancer, Volume 159, Issue 2, Page 410-422, 15 July 2026.
What's new? Monoclonal gammopathy of undetermined significance (MGUS) is an asymptomatic precursor to multiple myeloma, sharing substantial genetic features with overt malignancy. Given evidence implicating autophagy in myeloma risk, this study examined whether genetic variations in autophagy‐related genes influence MGUS susceptibility.
José Manuel Sánchez‐Maldonado   +54 more
wiley   +1 more source

Low-Grade Primary Splenic CD10-Positive Small B-Cell Lymphoma/Follicular Lymphoma

open access: yesCurrent Oncology, 2021
Primary splenic lymphoma (PSL) is a rare malignancy representing about 1% of all lymphoproliferative disorders, when using a strict definition that allows only involvement of spleen and hilar lymph nodes. In contrast, secondary low-grade B-cell lymphomas
Rami Abdulbaki   +4 more
doaj   +1 more source

Clinical, laboratory and ultrasonographic findings differentiating low‐grade intestinal T‐cell lymphoma from lymphoplasmacytic enteritis in cats

open access: yesJournal of Veterinary Internal Medicine, 2021
Background Low‐grade intestinal T‐cell lymphoma (LGITL) is the most common intestinal neoplasm in cats. Differentiating LGITL from lymphoplasmacytic enteritis (LPE) is challenging because clinical signs, laboratory results, diagnostic imaging findings ...
V. Freiche   +7 more
semanticscholar   +1 more source

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

Lymphoplasmacytic lymphoma presenting as retinal hemorrhage

open access: yesCleveland Clinic Journal of Medicine, 2017
A 51-year-old woman with no significant medical history presented to her primary care physician because of blurred vision, increased fatigue, palpitations, and intermittent episodes of epistaxis.
Jose, Melendez-Rosado   +2 more
openaire   +2 more sources

Cutaneous Crystal‐Storing Histiocytosis With Marginal Zone Lymphoma. A Case Report With A Striking Clinical Presentation

open access: yesJournal of Cutaneous Pathology, Volume 53, Issue 7, Page 576-580, July 2026.
ABSTRACT Cutaneous crystal‐storing histiocytosis (CSH) is an extremely rare histopathologic finding of histiocytes accumulating crystals of immunoglobulin or paraproteins, often associated with lymphoplasmacytic malignancies. It commonly presents in a wide age range of both female and male adults with a history of a lymphoproliferative disorder ...
Ashton Arlen   +3 more
wiley   +1 more source

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