Results 131 to 140 of about 22,024 (247)

Rosai-Dorfman Disease (Sinus Histiocytosis with Massive Lymphadenopathy): A Case Report

open access: yes, 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  

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

open access: yes
Brain Pathology, Volume 36, Issue 4, July 2026.
Alyssa M. Lee   +3 more
wiley   +1 more source

Solitary Langerhans cell histiocytosis of the hard palate: a diagnostic pitfall

open access: yes, 2016
Langerhans cell histiocytosis (LCH) is a relatively rare and unique disease characterized by an abnormal proliferation of immature dendritic cells. It is predominantly seen in children with adults showing less than ten times the incidence compared to ...
Varsha, Dalal   +7 more
core   +1 more source

Fear of Progression in Pediatric Cancer Patients and Their Parents: Trajectories, Prevalence, and Correlates Across Acute Treatment and Follow‐Up Care

open access: yesPsycho-Oncology, Volume 35, Issue 6, June 2026.
ABSTRACT Purpose Fear of progression (FoP) represents a significant psychological burden for pediatric cancer patients and their parents. This study investigates FoP levels across acute treatment (AcT) and follow‐up care (FuC) and examines trajectories over time, associated sociodemographic factors, and parent‐child associations.
Jessy Herrmann   +6 more
wiley   +1 more source

Aosta Valley animal cancer registry: A collaborative initiative for monitoring cancer burden in animals

open access: yesVeterinary Record Open, Volume 13, Issue 1, June 2026.
Abstract Background Animal cancer registry data are important for monitoring animal health, for prevention and research in veterinary medicine, and for comparative oncology. Since people and animals share the same environment and are exposed to many common risk factors, cancer patterns in animals may have a sentinel function for human health.
Claudio Trentin   +10 more
wiley   +1 more source

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

open access: yes
American Journal of Hematology, Volume 101, Issue 6, Page 1269-1272, June 2026.
Stephanie Quon   +5 more
wiley   +1 more source

Langerhans’ cell histiocytosis (histiocytosis X): A rare and diverse group of disorder in children

open access: yes, 2017
Langerhans cell histiocytosis is a rare disorder of unknown etiology with proliferation of Langerhans’ cells which may infiltrate a single or multiple organs.
Prajapati, Snehal   +2 more
core  

Adult langerhans cell histiocytosis

open access: yes, 2007
Langerhans cell histiocytosis is a group of idiopathic disorders characterized by the abnormal proliferation of specialized bone marrow-derived Langerhans cells. There are one to two cases per million population.
Bahceci, Mithat   +4 more
core  

An 11‐Month‐Old Infant With Unusual Diaper Dermatitis

open access: yes
JEADV Clinical Practice, Volume 5, Issue 2, Page 731-733, June 2026.
Majda Chaoui   +2 more
wiley   +1 more source

Treatment of Langerhans Cell Histiocytosis

open access: yes, 1996
Histiocytosis X patients present with a variety of clinical manifestations and outcomes. The principal difficulty in the establishment of a definite protocol for treatment is based on the poor understanding of the basic nature of this disease, the ...
김현우, 신규호
core  

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