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Lingual juvenile xanthogranuloma in a woman: a case report [PDF]
Introduction Juvenile xanthogranuloma is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. The presence of single or multiple raised cutaneous lesions characterize this self-healing disorder.
Villa Francesco+2 more
doaj +5 more sources
Juvenile xanthogranuloma manifesting in the forehead: A case report. [PDF]
Juvenile Xanthogranuloma. Key Clinical Message A 3 ‐year‐old boy presented with a forehead nodular mass, which was excised and confirmed histologically as Juvenile Xanthogranulomma (JXG). It affects children with a predilection for the head and neck region.
Chindia ML+3 more
europepmc +2 more sources
Erdheim-Chester Disease Presenting as Bilateral Facial Masses: A case report and review of literature. [PDF]
Erdheim-Chester disease (ECD) is a rare form of non-Langerhans cell histiocytosis with unknown etiology. It is recently recognized to be neoplastic with genetic mutations affecting the mitogen-activating protein kinase (MAPK) pathway.
Qureshi A+4 more
europepmc +3 more sources
Xanthogranulomatous Epithelial Tumor: A Case Report With 1-Year Follow-Up. [PDF]
Clinical Case Reports, Volume 12, Issue 12, December 2024.
AbuHejleh M+4 more
europepmc +2 more sources
Visualizing Touton Giant Cells Under Reflectance Confocal Microscopy in Two Cases of Juvenile Xanthogranuloma [PDF]
Peirano, Dominga+7 more
openaire +8 more sources
Pediatric Necrobiotic Xanthogranuloma as a Novel Phenotype of IKAROS Gain of Function. [PDF]
Guess R+4 more
europepmc +3 more sources
Upper eyelid juvenile xanthogranuloma: a case report
Juvenile xanthogranuloma is a rare benign non-Langerhans cell histiocytosis. Clinical manifestation usually occurs up to the age of 2 years, with yellowish papules and variable clinical progression.
Pedro Henrique Oliveira Ribeiro+4 more
doaj +1 more source
Juvenile xanthogranuloma (JXG) is the most common type of non-Langerhans cell histiocytosis. JXG is a rare benign tumor, which may be present at birth or develop later. The classical form of JXG is characterized by a red-yellowish benign papule or nodule
Kaspar Itin+3 more
doaj +1 more source
Disseminated Juvenile Xanthogranuloma: A Case Report
Introduction:. Histiocytoses are localized or systemic diseases that can broadly be classified into Langerhans cell histiocytosis and non-Langerhans cell histiocytosis.
Najam Us Saher+2 more
doaj +1 more source
The simultaneous existence of two classifications of haemato‐lymphoid tumours poses problems not only for diagnosis formulation but also for patients' management and design of clinical trials. Summary Since the publication in 2017 of the revised 4th Edition of the World Health Organization (WHO) classification of haematolymphoid tumours, here referred ...
Brunangelo Falini+2 more
wiley +1 more source