Results 21 to 30 of about 76 (72)

A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening

open access: yes
Brain Pathology, EarlyView.
Alyssa M. Lee   +3 more
wiley   +1 more source

Think highly of immunoglobulin G4‐related chronic rhinosinusitis as a clinical entity in immunoglobulin G4‐related disease

open access: yesEye &ENT Research, Volume 2, Issue 3, Page 151-163, September 2025.
Abstract IgG4‐related chronic rhinosinusitis (IgG4‐related CRS) is gaining recognition among various specialized physicians. As a systemic disease involving multiple organs, IgG4‐related CRS is still not widely recognized as an independent clinical entity. Given the complexity of diagnosing autoimmune‐related multisystem diseases, early recognition and
Lianqi Wan   +3 more
wiley   +1 more source

Analysis of Hyperexpanded T Cell Clones in SARS‐CoV‐2 Vaccine‐Associated Liver Injury by Spatial Proteomics and Transcriptomics

open access: yesLiver International, Volume 45, Issue 7, July 2025.
ABSTRACT Background and Aims SARS‐CoV‐2 vaccine‐associated liver injury (SVALI) is a rare event and its pathophysiology remains unclear. Previous studies have found an oligoclonal CD8+ T cell infiltrate and SARS‐CoV‐2 spike antigen‐specific T cells in the liver of patients with SVALI. Therefore, we aimed to characterise the immune infiltrate in a liver
Sarp Uzun   +11 more
wiley   +1 more source

Characteristics of histiocytic neoplasms presenting as breast masses

open access: yes
British Journal of Haematology, Volume 208, Issue 1, Page 358-362, January 2026.
Theodore Vougiouklakis   +10 more
wiley   +1 more source

Rosai‐Dorfman Disease in a 4‐Month‐Old Female Presenting With Cervical Lymphadenopathy

open access: yesClinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Rosai‐Dorfman disease is a rare histiocytic disorder that can mimic malignancies. This case highlights the importance of immunohistochemistry in distinguishing RDD from lymphoproliferative neoplasms, ensuring accurate diagnosis and management.
Allahdad Khan   +5 more
wiley   +1 more source

Role of liver biopsy in the management of idiosyncratic DILI

open access: yesLiver International, Volume 45, Issue 3, March 2025.
Abstract Drug‐induced liver injury (DILI) presents unique challenges in clinical practice. While some types of DILI are mild and resolve quickly after removing the drug, other situations are more complex, with competing aetiologies or underlying liver disease.
David E. Kleiner
wiley   +1 more source

Prednisone and Vincristine for the Treatment of Pediatric Rosai–Dorfman Disease: A Case Report

open access: yesCase Reports in Medicine, Volume 2025, Issue 1, 2025.
Purpose Pediatric Rosai–Dorfman disease (RDD) is extremely rare, and the current treatment plan is not unified. We hope that our study provides new ideas for the clinical treatment of RDD. Methods We report a case in which RDD was successfully treated with prednisone and vincristine, resulting in regression of enlarged lymph nodes.
Jianxin Dun   +5 more
wiley   +1 more source

Alterazioni stromali midollari nella mielofibrosi primitiva e secondaria: caratterizzazione clinicopatologica e implicazioni prognostiche [PDF]

open access: yes
Presupposti dello studio. Le neoplasie mieloproliferative (MPN) con fibrosi midollare comprendono la Mielofibrosi Primitiva (PMF) e Mielofibrosi secondarie (SMF) ad altre MPN.

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Unveiling the Gray: A Rare Case of Gray Platelet Syndrome With Hepatomegaly and Immune Dysregulation in a 14‐Year‐Old

open access: yesCase Reports in Hematology, Volume 2025, Issue 1, 2025.
Gray platelet syndrome (GPS) is a rare inherited platelet disorder characterized by the presence of gray platelets on blood smears, resulting from a deficiency of α‐granules. The thrombocytopenia presents in a spectrum of bleeding tendencies, varying among different patients.
Muhammad Takhman   +5 more
wiley   +1 more source

Modello di zebrafish di micosi fungoide [PDF]

open access: yes
Presupposti dello studio La micosi fungoide (MF) è la forma di linfoma primitivo cutaneo a cellule T più frequente, caratterizzata da un decorso clinico indolente e dalla progressione attraverso i tre diversi stadi di chiazza, placca e nodulo tumorale ...

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