Results 81 to 90 of about 31,333 (185)

Iatrogenic lymphoproliferative disorder [PDF]

American Journal of Hematology, 2014
Kamyar, Nader, Danielle Smith, Behrens, Chady Abboud, Leon, Roland, Schwarting, Andres, Ferber   +4 more
openaire   +2 more sources

Iptacopan for Immune Thrombocytopenia and Cold Agglutinin Disease: A Global Phase 2 Basket Clinical Trial

American Journal of Hematology, Volume 101, Issue 2, Page 242-254, February 2026.
ABSTRACT Iptacopan is a first‐in‐class, oral, selective inhibitor of complement factor B that has demonstrated positive efficacy across several complement‐driven diseases. Here we evaluate the efficacy and safety of iptacopan monotherapy in adult patients with primary immune thrombocytopenia (ITP) and primary cold agglutinin disease (CAD). We performed
Alexander Röth, Wilma Barcellini, Christine Ademokun, Junho Jang, Maria Luisa Lozano, David Valcarcel Ferreiras, Cristina Pascual‐Izquierdo, Shripad Chitnis, Sofiya Matviykiv, Alessandra Vitaliti, Chi Chen, Vasiliki Katsanou, Raghav Chawla, Hanny Al‐Samkari   +13 more
wiley   +1 more source

Conjugal Secondary Syphilis With Divergent Cutaneous Manifestations: Papulonodular Variant

Clinical Case Reports, Volume 14, Issue 2, February 2026.
Secondary syphilis (Papulonodular variant). Multiple erythematous papules and nodules on the (a) left side of the neck, (b) posterior neck, and (c) face. (d) Solitary indurated, erythematous papule over the shaft of the penis (arrow). ABSTRACT Syphilis should be considered in patients with atypical papulonodular eruptions, as even conjugal cases may ...
Mahesh Mathur, Sumit Paudel, Sandhya Regmi, Nabita Bhattarai, Shilpa Maharjan, Sambidha Karki   +5 more
wiley   +1 more source

Lymphoproliferative lung disorders: clinicopathological aspects [PDF]

European Respiratory Review, 2013
Venerino Poletti, Claudia Ravaglia, Sara Tomassetti, Carlo Gurioli, Gianluca Casoni, Silvia Asioli, Alessandra Dubini, Sara Piciucchi, Marco Chilosi   +8 more
doaj   +1 more source

What Is Your Diagnosis? Multiple Subcutaneous Lumps in a Horse

Veterinary Clinical Pathology, EarlyView.
Federica Meistro, Maria Virginia Ralletti, Riccardo Rinnovati, Alessandro Spadari, Maria Morini   +4 more
wiley   +1 more source

Miliary Tuberculosis With Immune Thrombocytopenia in 50‐Year‐Old Ethiopian Woman: A Case Report and Brief Review of Literature

Clinical Case Reports, Volume 14, Issue 2, February 2026.
Diffuse petechiae and non‐palpable purpura (lower extremities below knee, admission photo). ABSTRACT Immune thrombocytopenia (ITP) is a rare but recognized hematologic complication of tuberculosis (TB), particularly miliary TB. We present a case of a 50‐year‐old female with severe thrombocytopenia and hemorrhagic manifestations secondary to miliary TB.
Hayatu Awel Abdela, Tamirat Godebo Woyimo, Ragasa Getachew Bayisa, Sisay Tagese Tafese   +3 more
wiley   +1 more source

Auer Rod‐Like Inclusions in Chronic Lymphocytic Leukemia: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Auer rod‐like inclusions may occasionally be observed in chronic lymphocytic leukemia. Their recognition on peripheral smear highlights the importance of meticulous morphology assessment when comprehensive hematologic testing cannot be performed.
Tingting Zhang, Linjun Xie
wiley   +1 more source

Post-Transplant Lymphoproliferative Disorders

The Oncologist, 2006
Learning Objectives After completing this course, the reader will be able to: Discuss the incidence and pathologic classification of PTLD.Define the etiology and risk factors for PTLD.Discuss the presenting clinical features and diagnostic evaluation of PTLD.Describe treatments and reported outcomes for PTLD.
openaire   +2 more sources

Epstein‐Barr Virus Infection at Single‐Cell Resolution

Journal of Medical Virology, Volume 98, Issue 2, February 2026.
ABSTRACT Epstein‐Barr virus (EBV) infection has been studied at single‐cell resolution for six decades and counting. Such investigations can reveal virus‐host interactions and their dependence on viral strain, cellular niche, infection program, immune response regulation, and time.
Elliott D. SoRelle
wiley   +1 more source

DOCK8 deficiency presenting with sclerosing cholangitis, raised immunoglobulin E, and bronchiectasis: A fatal pediatric case report

JPGN Reports, Volume 7, Issue 1, Page 11-13, February 2026.
Abstract Dedicator of cytokinesis 8 (DOCK8) deficiency is a rare autosomal recessive primary immunodeficiency. Patients with DOCK8 deficiency typically present at early age with allergic manifestations, cutaneous and respiratory infections, raised immunoglobulin E, and they have an increased risk of developing malignancies.
Natalia Nedelkopoulou, Kelechi Ugonna, Stephen Hughes, Sanjay Rajwal, Marumbo Mtegha   +4 more
wiley   +1 more source