Abstract
Juvenile xanthogranulomas (JXGs) are benign cutaneous lesions of childhood that often spontaneously involute. They rarely present as a noncutaneous tumors. However, JXG tumors have been described in numerous noncutaneous anatomic sites, presenting with a variety of symptoms. The severity of symptoms and accurate preoperative diagnosis of JXG should determine operative and nonoperative treatment options of these uncommon, benign, and self-limiting tumors. We report 3 cases of symptomatic, noncutaneous JXG from disparate anatomic sites all treated with aggressive surgical resection.
Original language | English (US) |
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Pages (from-to) | 641-645 |
Number of pages | 5 |
Journal | Journal of Pediatric Hematology/Oncology |
Volume | 36 |
Issue number | 8 |
DOIs | |
State | Published - Nov 8 2014 |
Keywords
- Childhood
- Juvenile xanthogranuloma
- Lung tumor
- Pancreatic head mass
- Trigeminal nerve tumor
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Hematology
- Oncology