Abstract |
Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis of an unknown origin. The prognosis of ECD is variable, and it mainly depends on the involved anatomic sites. The treatment modalities have not been standardized. Interferon-alpha (IFN) has been reported to be effective in the management of ECD. We report here on an uncommon case with ECD in a 17-year-old female who had multiple lesions in the whole body and she was treated with chemotherapy and IFN. She has remained disease-free for 2 years after the completion of treatment.
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Authors | In-sang Jeon, Sang Seon Lee, Min Kyung Lee |
Journal | Pediatric blood & cancer
(Pediatr Blood Cancer)
Vol. 55
Issue 4
Pg. 745-7
(Oct 2010)
ISSN: 1545-5017 [Electronic] United States |
PMID | 20589628
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright 2010 Wiley-Liss, Inc. |
Chemical References |
- Interferon-alpha
- Vinblastine
- Prednisone
- Methotrexate
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Topics |
- Adolescent
- Erdheim-Chester Disease
(diagnosis, drug therapy)
- Female
- Humans
- Interferon-alpha
(therapeutic use)
- Methotrexate
(administration & dosage)
- Prednisone
(administration & dosage)
- Vinblastine
(administration & dosage)
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