Results 81 to 90 of about 99,753 (275)
Angioimmunoblastic T-cell lymphoma (AITL) is a malignant hematologic tumor arising from T follicular helper (Tfh) cells. High-throughput genomic sequencing studies have shown that AITL is characterized by a novel highly recurring somatic mutation in RHOA,
Fenglian Que+5 more
semanticscholar +1 more source
Loss of 5-hydroxymethylcytosine is a frequent event in peripheral T-cell lymphomas. [PDF]
International ...
Bernard, O.A.+12 more
core +2 more sources
Association Between Moraxella catarrhalis and Nodular Lymphocyte‐Predominant Hodgkin Lymphoma
ABSTRACT Nodular lymphocyte‐predominant Hodgkin Lymphoma (NLPHL) may be an antigen‐driven malignancy. Recent studies demonstrated that in NLPHL patients, lymphoma B‐cell receptor can bind proteins derived from Moraxella catarrhalis (MC) and Rothia mucilaginosa (RM). We examined whether MC and RM can be detected in NLPHL lymph nodes.
Izidore S. Lossos+7 more
wiley +1 more source
Recent studies have shown that follicular helper T‐cell lymphoma of angioimmunoblastic type (AITL), the most common nodal peripheral T‐cell lymphoma (PTCL), frequently arises in a background of clonal haematopoiesis (CH), a preneoplastic condition ...
Antonio Vogelsberg+7 more
semanticscholar +1 more source
Summary Peripheral T‐cell lymphoma (PTCL) is relatively prevalent in Asian populations. Previous studies suggest that germline mutations in familial haemophagocytic lymphohistiocytosis (FHL)‐related genes may predispose individuals to lymphoproliferative disorders.
Chong Wei+4 more
wiley +1 more source
Summary Data on late morbidity and survival in nodal peripheral T‐cell lymphoma (PTCL) are scarce. This study investigated the incidence, subtype distribution, late morbidity and survival outcomes of nodal PTCL in Finland. The study compared 998 patients with nodal PTCL diagnosed between 2007 and 2019 with matched controls.
Anu Partanen+7 more
wiley +1 more source
Angioimmunoblastic T Cell Lymphoma Mimicking Chronic Urticaria
Angioimmunoblastic T cell lymphoma (AITL) is a rare but distinct type of T cell lymphoma with an aggressive course and high mortality. Most patients are diagnosed late in the disease and usually present with generalized lymphadenopathy.
Mohleen Kang+3 more
doaj +1 more source
Non-ST Elevation MI as a Unique Presentation of Angioimmunoblastic T-cell Lymphoma [PDF]
Case A 61-year-old Chinese female with a history of hypertension, hyperlipidemia, asthma, and gastroesophageal reflux disease presented with four days of chest pressure that radiated to her left arm and jaw.
Chandra, MD, Avinash+4 more
core +2 more sources
ABSTRACT Background T‐cell receptor constant beta chain 1 (TRBC1) has emerged as a potential clonal marker for T‐cell lymphoma. This study evaluated TRBC1 expression using flow cytometry in healthy individuals and various clinical specimens, assessing its clinical utility in the diagnosis of T‐cell lymphomas.
SooHo Yu+4 more
wiley +1 more source
Hypercalcemia as a rare presentation of angioimmunoblastic T cell lymphoma: a case report
Background Angioimmunoblastic T cell lymphoma is a rare malignancy, accounting for only 2% of all non-Hodgkin lymphomas, first described in the 1970s and subsequently accepted as a distinct entity in the current World Health Organization classification ...
Sana Chams+4 more
doaj +1 more source