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Adult Onset Orbital Xanthogranuloma, a Variant of Adult Orbital Xanthogranulomatous Disease: An Infrequent Entity. [PDF]
Lakavarapukota S+3 more
europepmc +1 more source
A Solitary Hyperpigmented Nodule on the Calf of a Young Boy.
Saha A, Sardar S, Dhar S, Chandra A.
europepmc +1 more source
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Dermoscopy of Juvenile Xanthogranuloma
Dermatology, 2020Background: Dermoscopy is useful for the evaluation of juvenile xanthogranuloma (JXG). The classical “setting sun” pattern is characteristic of JXG, but its sensibility appears to be limited.
L. Peruilh-Bagolini+6 more
semanticscholar +4 more sources
Systemic juvenile xanthogranuloma: A systematic review
Pediatric Blood & Cancer, 2023To perform a systematic review to investigate the available literature regarding systemic juvenile xanthogranuloma (SJXG) and report the population characteristics, clinical manifestation, therapy, and outcome.
Tong Zou+10 more
semanticscholar +1 more source
Alectinib In the Treatment of Systemic Juvenile Xanthogranuloma of Infancy With ALK Translocation.
JAMA dermatology, 2023This observational case series examines the diagnosis and treatment of 2 patients with systemic juvenile xanthogranuloma treated with alectinib.
Jiaosheng Xu+5 more
semanticscholar +1 more source
Langerhans Cell Histiocytosis Evolving into Juvenile Xanthogranuloma: Two Linked Entities
American journal of dermatopathology, 2023Background: Langerhans cell histiocytosis (LCH) represents a myeloid clonal proliferation that involves the skin and other organs. Occasionally, cases of LCH evolve into juvenile xanthogranuloma (JXG).
Nada Shaker, O. Sangueza
semanticscholar +1 more source
Journal of the European Academy of Dermatology and Venereology, 2022
To the Editor, Juvenile xanthogranuloma (JXG) is a type of non-Langerhans cell histiocytosis characterized by benign proliferation of macrophages and dendritic cells.
P. Gupta+4 more
semanticscholar +1 more source
To the Editor, Juvenile xanthogranuloma (JXG) is a type of non-Langerhans cell histiocytosis characterized by benign proliferation of macrophages and dendritic cells.
P. Gupta+4 more
semanticscholar +1 more source
Clinica Terapeutica, 2022
Neurofibromatosis type 1 (NF1), is a rare genetic disorder that may involve almost every organ system in the body such as cutaneous, ophthalmologic and central and peripheral nervous system.
E. Miraglia+3 more
semanticscholar +1 more source
Neurofibromatosis type 1 (NF1), is a rare genetic disorder that may involve almost every organ system in the body such as cutaneous, ophthalmologic and central and peripheral nervous system.
E. Miraglia+3 more
semanticscholar +1 more source