Successful sirolimus treatment of spindle cell haemangiomas in a paediatric patient with Maffucci syndrome
Author:
Affiliation:
1. Departments of Dermatology
2. Burn and Plastic Surgery
3. Pathology, Beijing Children’s Hospital, Capital Medical University, National Center for Children’s Health , Beijing , China
Abstract
Funder
Beijing Natural Science Foundation
Open Project of Henan Clinical Research Center of Childhood Diseases
Publisher
Oxford University Press (OUP)
Link
https://academic.oup.com/ced/advance-article-pdf/doi/10.1093/ced/llae018/56721129/llae018.pdf
Reference8 articles.
1. A prospective multicenter study of sirolimus for complicated vascular anomalies;Ji;J Vasc Surg,2021
2. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome;Pansuriya;Nat Genet,2011
3. Mutational analysis using Sanger and next generation sequencing in sporadic spindle cell hemangiomas: a study of 19 cases;Ten Broek;Genes Chromosomes Cancer,2017
4. Maffucci's syndrome: functional and neoplastic significance. Case report and review of the literature;Lewis;J Bone Joint Surg Am,1973
5. Maffucci's syndrome with oral and intestinal haemangioma;Lee;Br J Dermatol,1999
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