Results 11 to 20 of about 3,140 (170)

Splenic, Nonhairy, B-Cell Lymphoma Presenting as Fever of Unknown Origin [PDF]

open access: yesCase Reports in Medicine
Fever of unknown origin (FUO) is a common diagnostic dilemma faced by internists on a fairly regular basis. A wide variety of infectious, autoimmune, and neoplastic conditions can present with FUO.
Abdul Rehman   +4 more
doaj   +2 more sources

Non‐V600E BRAF mutation in hairy cell leukemia variant [PDF]

open access: yeseJHaem
Anjanaa Vijayanarayanan   +5 more
doaj   +2 more sources

Hairy cell leukemia variant [PDF]

open access: yesJournal of Hematopathology, 2010
Manuela Mollejo   +2 more
exaly   +2 more sources

Hairy Cell Leukemia Variant [PDF]

open access: yesAmerican Journal of Clinical Pathology, 2005
Hairy cell leukemia variant (HCL-V) is a poorly described, rare B-cell lymphoproliferative disorder typically positive for CD103 and CD11c, while lacking CD25. Splenic marginal zone lymphomas (SMZL) also have this unusual phenotype in 15% to 25% of cases, have other overlapping clinical or morphologic features, and are more common than HCL-V.
Melissa H, Cessna   +4 more
  +5 more sources

A Hairy Cell Leukaemia Variant – A Rare Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
The aim of the article is to present a rare case of Hairy cell leukaemia variant (HCl-V) which is a distinct clinico-pathological entity with intermediate features between classical HCl (HCl-C) and B-cell prolymphocytic leukaemia.
Pankaj Pande   +2 more
doaj   +1 more source

Hairy Cell Leukemia with Marrow Reactive Plasmacytosis and Mast Cell Hyperplasia: A Case Report and Brief Review of the Literature [PDF]

open access: yesJournal of Kerman University of Medical Sciences, 2023
Hairy cell leukemia (HCL) and HCL-like disorders, including HCL-variant, are disorders of heterogeneous mature lymphoid B-cells known for their hairy cell infiltration accompanied by a specific genetic profile, various clinical presentations, and, as ...
Elham Jafari   +2 more
doaj   +1 more source

CD5-Negative, CD10-Negative Low-Grade B-Cell Lymphoproliferative Disorders of the Spleen

open access: yesCurrent Oncology, 2021
CD5-negative, CD10-negative low-grade B-cell lymphoproliferative disorders (CD5-CD10-LPD) of the spleen comprise a fascinating group of indolent, neoplastic, mature B-cell proliferations that are essential to accurately identify but can be difficult to ...
John J. Schmieg   +3 more
doaj   +1 more source

Flowcytometry aiding morphological diagnosis of mature B-cell neoplasm in patients with lymphocytosis

open access: yesMedical Journal of Babylon, 2021
Background: Mature B-cell neoplasms (MBCNs) are a category of disorders with a broad range of clinical manifestations, pathologic features, and outcomes that share common characteristics.
Husham Raad Abbas   +1 more
doaj   +1 more source

Rare case of plasma cell myeloma with megakaryoblastic morphology mimicking acute leukemia

open access: yesIndian Journal of Pathology and Microbiology, 2020
Myeloma plasma cells vary from mature forms to immature, plasmablastic, and pleomorphic cells. Only a few cases of morphologic variant of plasma cell neoplasm have been reported, in which the plasma cell neoplasm presented with lymphoplasmacytic ...
Keyu Liu   +5 more
doaj   +1 more source

Constant activation of the RAF-MEK-ERK pathway as a diagnostic and therapeutic target in hairy cell leukemia

open access: yesHaematologica, 2013
The BRAF-V600E mutation defines genetically hairy cell leukemia among B-cell leukemias and lymphomas. In solid tumors, BRAF-V600E is known to aberrantly activate the oncogenic MEK-ERK pathway, and targeted BRAF and/or MEK inhibitors have shown remarkable
Enrico Tiacci   +14 more
doaj   +1 more source

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