Neonatal Systemic Juvenile Xanthogranuloma with an Ominous Presentation and Successful Treatment

This case report originated from a case of neonatal multisystemic juvenile xanthogranuloma (JXG). The patient presented with blue muffin rush, cervical mass, bone destruction, lung nodule, hepatosplenomegaly, and coagulopathy and was successfully treated with Langerhans cell histiocytosis (LCH) base...

Descripción completa

Detalles Bibliográficos
Autores principales: Fan, Rong, Sun, Jihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117631/
https://www.ncbi.nlm.nih.gov/pubmed/21695102
http://dx.doi.org/10.4137/CMO.S6686

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117631/
https://www.ncbi.nlm.nih.gov/pubmed/21695102
http://dx.doi.org/10.4137/CMO.S6686

Ejemplares similares