Renal infarction due to polyarteritis nodosa in a patient with angioimmunoblastic T-cell lymphoma: a case report and a brief review of the literature [PDF]
Diagnostic Pathology, 2012 Angioimmunoblastic T-cell lymphoma is one of the most common subtypes of peripheral T-cell lymphoma (15-20% of all cases), accounting for approximately 1-2% of all non-Hodgkin lymphomas.
Ambrosio Maria +7 more
doaj +6 more sources
Angioimmunoblastic T-cell lymphoma: the many-faced lymphoma [PDF]
Blood, 2017 AbstractAngioimmunoblastic T-cell lymphoma (AITL) is an uncommon subtype of mature peripheral T-cell lymphoma (PTCL). The history of AITL is much longer and deeper than the literature would suggest given the many names that have preceded it. Advanced-stage disease is common with uncharacteristic laboratory and autoimmune findings that often slow or ...
Matthew A. Lunning, Julie M. Vose
semanticscholar +5 more sources
Advances in understanding of angioimmunoblastic T-cell lymphoma [PDF]
Leukemia, 2020 AbstractIt has been nearly half a century since angioimmunoblastic T-cell lymphoma (AITL) was characterized in the early 1970’s. Our understanding of the disease has dramatically changed due to multiple discoveries and insights. One of the key features of AITL is aberrant immune activity.
Shigeru Chiba +1 more
semanticscholar +4 more sources
Angioimmunoblastic T-cell lymphoma presenting as giant kidneys: a case report [PDF]
Journal of Medical Case Reports, 2009 Introduction Angioimmunoblastic T-cell lymphoma is a rare form of tumor of the lymph nodes or lymphoid tissue. In this report we describe an unusual presentation of angioimmunoblastic T-cell lymphoma consisting of giant kidneys with no nephrotic syndrome.
Argov Ori +3 more
doaj +4 more sources
Spontaneous remission of angioimmunoblastic T-cell lymphoma in a child with ataxia–telangiectasia: a case report [PDF]
Journal 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 +2 more sources
Angioimmunoblastic T-Cell Lymphoma: A Questionable Association with Follicular Dendritic Cell Sarcoma [PDF]
Case Reports in Hematology, 2017 An elderly woman presented with generalized lymphadenopathy, several systemic symptoms, and splenomegaly. An inguinal lymph node excision revealed a compound picture.
Daniel Benharroch +2 more
doaj +3 more sources
Targeting intratumoral B cells with rituximab in addition to CHOP in angioimmunoblastic T-cell lymphoma. A clinicobiological study of the GELA. [PDF]
, 2012 Background In angioimmunoblastic T-cell lymphoma, symptoms linked to B-lymphocyte activation are common, and variable numbers of CD20(+) large B-blasts, often infected by Epstein-Barr virus, are found in tumor tissues.
Bouabdallah, R. +15 more
core +4 more sources
Angioimmunoblastic T-Cell Lymphoma: A Diagnostic Challenge [PDF]
Case 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 +5 more sources
Pleuropneumonia Revealing Angioimmunoblastic T-cell Lymphoma. [PDF]
CureusAngioimmunoblastic 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
Composite Angioimmunoblastic T-Cell Lymphoma and Diffuse Large B-Cell Lymphoma Presenting with Distributive Shock [PDF]
Hematology Reports, 2023 Diffuse large B-cell lymphoma (DLBCL) and angioimmunoblastic T-cell lymphoma (AITL) are two subtypes of non-Hodgkin lymphoma (NHL). The simultaneous occurrence of DLBCL and AITL in a composite lymphoma is very rare, and there are no established treatment
Nisha Hariharan +4 more
doaj +2 more sources