Results 171 to 180 of about 316,660 (233)

A Solitary Hyperpigmented Nodule on the Calf of a Young Boy.

open access: yesIndian J Dermatol
Saha A, Sardar S, Dhar S, Chandra A.
europepmc   +1 more source

Dermoscopy of Juvenile Xanthogranuloma

Dermatology, 2020
Background: 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, 2023
To 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, 2023
This 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, 2023
Background: 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

Dermatoscopy and clinicopathological correlation of juvenile xanthogranuloma in skin of colour: a series of six patients

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

Juvenile xanthogranuloma in neurofibromatosis type 1. Prevalence and possible correlation with lymphoproliferative diseases: experience of a single center and review of the literature.

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

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