Cutaneous adult xanthogranuloma with a small portion of BRAF
BRAFV600E mutation
Langerhans cell histiocytosis
adult xanthogranuloma
emperipolesis
solitary cutaneous mixed histiocytoma
Journal
The Journal of dermatology
ISSN: 1346-8138
Titre abrégé: J Dermatol
Pays: England
ID NLM: 7600545
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
received:
03
08
2018
accepted:
06
11
2018
pubmed:
12
12
2018
medline:
29
5
2019
entrez:
12
12
2018
Statut:
ppublish
Résumé
Histiocytoses, including Langerhans cell histiocytosis (LCH), juvenile or adult xanthogranuloma (AXG) and Rosai-Dorfman disease (RDD), are rare disorders characterized by the proliferation of cells derived from monocyte/macrophage lineages. A few cases of LCH coexisting with xanthogranuloma or RDD have been reported. The etiology of these diseases remains unclear. However, oncogenic BRAF
Identifiants
pubmed: 30536719
doi: 10.1111/1346-8138.14725
doi:
Substances chimiques
BRAF protein, human
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Types de publication
Case Reports
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
161-165Informations de copyright
© 2018 Japanese Dermatological Association.