Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Juvenile xanthogranuloma: retrospective analysis of 44 pediatric cases (single tertiary care center experience).

International journal of dermatology - 1 May 2021

Kundak Selcen, Çakır Yasemin

Abstract excerpt

BACKGROUND/OBJECTIVE: Juvenile xanthogranuloma (JXG) is a rarely encountered skin disorder, which is characterized by the proliferation of non-Langerhans cell histiocytes. As JXG primarily affects infants and young children, this study aims to describe the epidemiologic, clinical, and histopathologic characteristics of 44 children diagnosed with JXG at a tertiary health care center. METHODS: Fourty-four children...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Mutation

Share to Tertiary Care Centers

Source

Identifiers

PMID: 33301172
DOI: 10.1111/ijd.15223

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Juvenile xanthogranuloma: retrospective analysis of 44 pediatric cases (single tertiary care center experience).PMID 33301172Read ↗

Oral Juvenile Xanthogranuloma: A Clinicopathological, Immunohistochemical and BRAF V600E Study of Five New Cases, with Literature Review.Semantic proximity Read ↗

BRAF V600E mutation in pediatric intracranial and cranial juvenile xanthogranuloma.Semantic proximity Read ↗

BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester disease.Semantic proximity Read ↗

Activating MAPK1 (ERK2) mutation in an aggressive case of disseminated juvenile xanthogranulomaSemantic proximity Read ↗

Refractory juvenile xanthogranuloma of the mastoid bone responsive to trametinibSemantic proximity Read ↗

NTRK1 Gene Fusions Are Frequent in Juvenile XanthogranulomaSemantic proximity Read ↗

Uncommon histiocytic disorders: Rosai-Dorfman, juvenile xanthogranuloma, and Erdheim-Chester disease.Semantic proximity Read ↗

Juvenile xanthogranuloma: A possible diagnostic criterion for Neurofibromatosis type 1 in young children.Semantic proximity Read ↗

Histiocytic Diseases of Neonates: Langerhans Cell Histiocytosis, Rosai-Dorfman Disease, and Juvenile Xanthogranuloma.Semantic proximity Read ↗

Clonality in Juvenile XanthogranulomaSemantic proximity Read ↗

Recurrent CLTC::SYK fusions and CSF1R mutations in juvenile xanthogranuloma of soft tissue.Semantic proximity Read ↗

Dabrafenib as a Therapeutic Option for Chemotherapy-Refractory pediatric Juvenile Xanthogranuloma: A Case ReportSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.