Results 111 to 120 of about 24,068 (238)
Nepal Journal of Dermatology, Venereology & Leprology, 2018 Non-Langerhans-Cell histiocytosis spectrum of disorders includes multicentric reticulohistiocytosis (MR) and multiple cutaneous reticulohistiocytomas (MCR), which are very uncommon granulomatous conditions. In reticulohistiocytoma, the most common sites
Karuna Singh Sijapati +2 more
doaj
Immune Checkpoint Inhibitor‐Induced Pancreatitis
United European Gastroenterology Journal, Volume 14, Issue 7, September 2026.ABSTRACT The increasing use of immune checkpoint inhibitors (ICI) has led to recognition of a broad spectrum of treatment‐associated inflammatory adverse events, including pancreatic injury. Histological overlap between ICI associated pancreatic injury (ICIPI) and so‐called autoimmune pancreatitis (AIP) has been suggested in isolated reports, but the ...
Carlos Fernandez Moro +9 more
wiley +1 more source
Clinical Genetics, Volume 110, Issue 3, Page 379-388, September 2026.Novel variants in PUS7 associated with intellectual disability and growth retardation: expanding the clinical spectrum in 13 patients. ABSTRACT Pseudouridylation is a frequent post‐transcriptional modification resulting in uridine isomerization in 5‐ribosyluracil, also called pseudouridine. This mechanism leads to RNA stability with an increase in base‐
Camille Bergès +30 more
wiley +1 more source
Histopathology, Volume 89, Issue 3, Page 403-425, September 2026.This review highlights changes relevant to pathologists in the updated multidisciplinary classification of interstitial pneumonias. Changes include expansion beyond idiopathic disease, subclassification as interstitial (fibrotic vs non‐fibrotic) and alveolar filling disorders, expansion to include additional patterns (e.g.
Andrew G Nicholson +7 more
wiley +1 more source
Rosai-Dorfman Disease (Sinus Histiocytosis with Massive Lymphadenopathy): A Case Report
, 2003 Rosai-Dorfman disease is a rare benign idiopatic histiocytic proliferative disorder. It is also known as sinus histiocytosis with massive lymphadenopathy.
Erkan Özüdoğru +4 more
core
[Unusual pulmonary presentation of systemic Langerhans cell histiocytosis]
, 2008 An 80-year-old nonsmoking man was referred to our hospital with bilateral perihilar pulmonary opacities. He had a history of epilepsy, sclerosing cholangitis, cutaneous lesions previously diagnosed as localised Langerhans cell histiocytosis.
Schuller, A +11 more
core +1 more source
Perineurioma‐like EMA‐positive calvarial neoplasms: clinicopathological study of eight cases
Histopathology, Volume 89, Issue 3, Page 544-553, September 2026.Perineurioma‐like, EMA‐positive calvarial neoplasms (PLECN) are a rare group of intraosseous spindle cell tumours that demonstrate overlapping morphologic features of perineurioma and fibroblastic meningioma. These lesions tend to behave indolently but show a propensity for progressive growth.
Raheel Rizwan +9 more
wiley +1 more source
Langerhans cell histiocytosis in monocygote twins: case reports.
, 1996 Langerhans cell histiocytosis includes three clinical forms of histiocytosis X. We describe a disseminated form of Langerhans cell histiocytosis (Letterer-Siwe disease) in monozygotic twins.
Mader I +3 more
core +1 more source