A benign fibrohistiocytic lesion that occurs during childhood; it is distinct from Langerhans cell histiocytosis. The lesions usually develop during infancy, and are characterized by regressing cutaneous nodules (most often in the head and neck) sometimes associated with deep soft tissues nodules. The prognosis is excellent. -- 2003

Literature | 796 results

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• A child with coexistent juvenile xanthogranuloma and Langerhans cell histiocytosis.

  Authors: Hong Yu, Jincheng Kong, Yan Gu, Bo Ling, Zhengjun Xi, Zhirong Yao

  Journal of the American Academy of Dermatology 2010 Feb

• Systemic juvenile xanthogranuloma with fatal outcome.

  Authors: Daniel Azorín, Antonio Torrelo, Alvaro Lassaletta, Inmaculada de Prada, Isabel Colmenero, Trinidad Contra, Imelda González-Mediero

  Pediatric dermatology 2009 Nov-Dec

Associated Researchers

Thought leaders and organizations working on research involving juvenile xanthogranuloma.

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• Don T Tran
• Antonio Torrelo
• Isabel Colmenero
• Patricio Pozo
• Eyas M Hattab

View All Clinical Trials Sponsors

• National Cancer Institute (NCI)

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• University of Washington
• Hospital for Sick Children
• Shanghai Jiaotong University Medical School
• Hospital del Niño Jesús
• University of Santiago de Compostela

Clinical Trials | 1 trial

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• Natural History Study of Patients With Neurofibromatosis Type I

  conditions: Neurofibromatosis Type 1 ; Malignant Peripheral Nerve Sheath Tumor ; Plexiform Neurofibroma ; Optic Glioma ; Neurofibroma

  interventions: none

   

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