Results 21 to 30 of about 76 (72)
A 50‐year‐old man with a 12‐year history of extensive pachymeningeal thickening
Brain Pathology, EarlyView.
Alyssa M. Lee +3 more
wiley +1 more source
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
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
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
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
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
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]
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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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]
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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