Results 141 to 150 of about 54,429 (272)

Management of post-transplant lymphoproliferative disorders

HemaSphere, 2019
Daan Dierickx, Vibeke Vergote
doaj   +1 more source

Interfollicular Plasmacytosis and Hyperplastic Germinal Centers in Idiopathic Multicentric Castleman Disease, Idiopathic Plasmacytic Lymphadenopathy Subtype

American Journal of Hematology, Volume 101, Issue 6, Page 1269-1272, June 2026.
Stephanie Quon, Clarissa Skorupski, Christophe Langlois, Lee Mozessohn, Carlo Hojilla, Luke Y. C. Chen   +5 more
wiley   +1 more source

Liver Transplantation Outcomes in Crigler‐Najjar Syndrome in Iran: A Single‐Center Retrospective Cohort Study Over 20 Years

Health Science Reports, Volume 9, Issue 5, May 2026.
ABSTRACT Background and Aims Crigler‐Najjar Syndrome (CNS) is a rare autosomal recessive disorder caused by uridine diphosphate glucuronosyltransferase (UGT1A1) deficiency, leading to unconjugated hyperbilirubinemia. Without treatment, patients are at high risk of kernicterus and irreversible neurological damage.
Sajad Teimoury, Zahra Beyzaei, Alireza Shamsaeefar, Kurosh Kazemi, Saman Nikeghbalian, Seyed‐Ali Malekhosseini, Bita Geramizadeh   +6 more
wiley   +1 more source

A05 | TP53 in lymphoproliferative neoplastic disorders

Haematologica
TP53 disruption represents a central event driving clonal evolution, therapeutic resistance, and adverse outcome in several B-cell neoplasms, including chronic lymphocytic leukemia (CLL), mantle cell lymphoma (MCL), and diffuse large B-cell lymphoma ...
Gian Matteo Rigolin
doaj  

Diagnostic criteria and new therapeutic options for patients diagnosed with non-Hodgkin lymphoma

Archivo Médico de Camagüey, 2019
Background: malignant haemopathies increase their incidence and proliferation within the population, among them the lymphoproliferative syndrome occupies an important place, it is a group of disorders of clonal origin, which affects the lymphoid cells ...
Yaimé Moreno-Laguard, Leonardo Laguna-Salvia, José Ignacio Larquin-Comet, Cira Cecilia León-Ramentol, Yadier Fermin Hernandez-Soler, Maurice José González-Basulto   +5 more
doaj  

Novel Laboratory Approaches in Heavy Chain Disease With Discordant Immunoglobulin Quantitation: A Case Report and Literature Review

Journal of Clinical Laboratory Analysis, Volume 40, Issue 9, May 2026.
In this study, we investigated a rare case of γ‐heavy chain disease (γ‐HCD) through an integrated laboratory approach. Routine protein analyses (serum protein electrophoresis, immunotyping, and serum/urine immunofixation) identified an IgG monoclonal component without detectable light chains.
Eleonora Longhi, Artan Çeka, Fabiola Olivieri, Marco Moretti, Jacopo Sabbatinelli   +4 more
wiley   +1 more source

HIV-associated lymphoproliferative disorders: Single-center experience. [PDF]

Medicine (Baltimore)
Demirtas D, Toptas T, Yilmaz AF, Erturk Sengel B, Yuksel T, Kokkaya YE, Candan O, Yanik AM, Salim S, Ulukoylu Menguc M, Arikan F, Atagunduz I, Korten V, Tuglular AT.   +13 more
europepmc   +1 more source

Comparative Analysis of Four Matrix Dilution Methods for Eliminating IgM Paraprotein Interference in Prealbumin and Uric Acid Assays: Based on Two Case Reports

Journal of Clinical Laboratory Analysis, Volume 40, Issue 9, May 2026.
IgM paraproteins can cause significant interference in prealbumin (PA) and uric acid (UA) measurements, leading to falsely abnormal results. We systematically compared four dilution methods to eliminate this interference. Dilution with the PA reagent (containing PEG) effectively restored accurate PA results.
Xiaowei Chi, Zihan Liu, Weifang Liu, Huihui Jiang, Denglu Zhang   +4 more
wiley   +1 more source

Pediatric lymphoproliferative disorders - Emerging insights and management: A narrative review. [PDF]

Medicine (Baltimore)
Obeagu EI.
europepmc   +1 more source

Putative Clonal Evolution in a PHF6‐Mutant T/NK‐Cell Lymphoproliferative Disorder With Selective Loss of a STAT5B‐Mutant Subclone

eJHaem, Volume 7, Issue 3, June 2026.
Mark Anthony Turingan, Cuihong Wei, Nihad Almokhtar, Abi Vijenthira, Hong Chang   +4 more
wiley   +1 more source