Results 1 to 10 of about 5,225 (148)

Cutaneous involvement in angioimmunoblastic T-cell lymphoma

open access: yesIndian Journal of Dermatology, 2010
Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive non-Hodgkin′s nodal peripheral T-cell lymphoma characterized by general lymphadenopathy, night sweats, fever, hepatosplenomegaly, polyclonal hypergammaglobulinemia, and cutaneous ...
Papadavid Evangelia   +5 more
doaj   +4 more sources

Immunoglobulinopathies in patients with angioimmunoblastic T-cell lymphoma [PDF]

open access: yesТерапевтический архив, 2018
Contex. Angioimmunoblastic T-cell lymphoma (AITL) is a rare form of non-Hodgkins lymphoma, characterized by generalized lymphadenopathy, hepatosplenomegaly and dysproteinemia. Hypergammaglobulinaemia is revealed in 50-83% pts with AITL.
N G CHERNOVA   +9 more
doaj   +4 more sources

Angioimmunoblastic T-Cell Lymphoma: A Diagnostic Challenge [PDF]

open access: yesCase Reports in Dermatology, 2014
Angioimmunoblastic T-cell lymphoma (AITL) accounts for 15-20% of all peripheral T-cell lymphomas. It is a rare subtype of CD4 T-cell peripheral lymphoma that affects aged individuals, causing B symptoms, generalized lymphadenopathy and hepatosplenomegaly.
Jorge Ocampo-Garza   +8 more
doaj   +4 more sources

Molecular diagnosis angioimmunoblastic T-cell lymphoma

open access: yesТерапевтический архив, 2019
Aim: to determine molecular diagnostics routine for different tissue samples in angioimmunoblastic T-cell lymphoma. Materials and methods. Molecular studies were performed for 84 primary AITL patients.
N G Chernova   +7 more
doaj   +3 more sources

Pleuropneumonia Revealing Angioimmunoblastic T-cell Lymphoma. [PDF]

open access: yesCureus
Angioimmunoblastic T-cell lymphoma (AITL) is a rare form of lymphoma that presents with a wide range of symptoms, including multiple lymphadenopathies, systemic symptoms, splenomegaly, hepatomegaly, and skin rashes. Due to its atypical presentation, diagnosis can be delayed, and confirmation relies on lymph node biopsy.
Salhi Z   +7 more
europepmc   +3 more sources

In vivo CAR T cell therapy against angioimmunoblastic T cell lymphoma [PDF]

open access: yesJournal of Experimental & Clinical Cancer Research
Background For angioimmunoblastic T cell lymphoma (AITL), a rare cancer, no specific treatments are available and survival outcome is poor. We previously developed a murine model for AITL that mimics closely human disease and allows to evaluate new ...
Adrien Krug   +7 more
doaj   +2 more sources

Angioimmunoblastic T-cell Lymphoma: A Mimic for Lupus

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2020
New-onset systemic lupus erythematosus (SLE) is uncommon in elderly patients. We report the case of a 71-year-old woman who was diagnosed with SLE based on clinical manifestations of fever, alopecia, bicytopenia, hepatomegaly, lymphadenopathy ...
Hui Boon Tay   +4 more
doaj   +3 more sources

Spontaneous remission of angioimmunoblastic T-cell lymphoma in a child with ataxia–telangiectasia: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Angioimmunoblastic T-cell lymphoma is an uncommon subtype of peripheral T-cell lymphoma in children with fewer than 20 cases reported in literature.
Dima Abla   +5 more
doaj   +1 more source

Peripheral T-Cell Lymphomas of the T Follicular Helper Type: Clinical, Pathological, and Genetic Attributes

open access: yesHemato, 2022
Follicular helper T-cell (TFH) lymphomas comprise a unique group of T-cell lymphomas that represent neoplastic proliferations of follicular helper T-cells and share genetic, immunophenotypic, morphologic, and clinical features.
Karthik A. Ganapathi   +2 more
doaj   +1 more source

Conjunctival Angioimmunoblastic T-Cell Lymphoma [PDF]

open access: yesOcular Oncology and Pathology, 2014
Angioimmunoblastic T-cell lymphoma (AITL) represents an uncommon variant of T-cell lymphomas and most often presents insidiously with systemic symptoms. This report constitutes the first documented case of conjunctival AITL, masquerading as nodular episcleritis, and describes both the clinical and pathological findings. Furthermore, conjunctival T-cell
Darshak S. Patel   +4 more
openaire   +2 more sources

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