Case 2: Soft Tissue Congenital Neck Mass
Author:
Affiliation:
1. Department of Neonatology and Pediatrics, and
2. Department of Hematology/Oncology and Pediatrics, University of New Mexico, Albuquerque, NM
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology, and Child Health
Link
https://publications.aap.org/neoreviews/article-pdf/20/8/e468/829825/neoreviews_012019iositn00006.pdf
Reference7 articles.
1. Uncommon histiocytic disorders: Rosai-Dorfman, juvenile xanthogranuloma, and Erdheim-Chester disease;Haroche;Hematology (Am Soc Hematol Educ Program),2015
2. Juvenile xanthogranulomas in the first two decades of life: a clinicopathologic study of 174 cases with cutaneous and extracutaneous manifestations;Dehner;Am J Surg Pathol,2003
3. Juvenile xanthogranuloma in childhood and adolescence: a clinicopathologic study of 129 patients from the kiel pediatric tumor registry;Janssen;Am J Surg Pathol,2005
4. Successful treatment of systemic juvenile xanthogranulomatosis with cytarabine and 2-chlorodeoxyadenosine: case report and review of the literature;Maintz;Br J Dermatol,2017
5. Clofarabine salvage therapy in refractory multifocal histiocytic disorders, including Langerhans cell histiocytosis, juvenile xanthogranuloma and Rosai-Dorfman disease;Simko;Pediatr Blood Cancer,2014
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