| Literature DB >> 26555222 |
Shengmei Zhou1,2, Larry Wang1,2, Andre Panossian2,3, Dean Anselmo2,3, Samuel Wu1,2, Rajkumar Venkatramani4.
Abstract
We report a 7-year-old male with a history of recurrent kaposiform hemangioendothelioma (KHE) in the sacral area and multiple thoracic vertebral lesions. Tumor karyotyping revealed the balanced translocation t(13;16)(q14;p13.3). He had mildly decreased platelet counts but never experienced any episodes of Kasabach-Merritt phenomenon. He was treated with vincristine for 1 year but improvement was minor. Significant clinical improvement was seen with sirolimus therapy. To the best of our knowledge, this is the first report to demonstrate that KHE is associated with a clonal karyotypic abnormality.Entities:
Keywords: chromosomal translocation; kaposiform hemangioendothelioma; sirolimus
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Year: 2015 PMID: 26555222 DOI: 10.2350/15-09-1707-CR.1
Source DB: PubMed Journal: Pediatr Dev Pathol ISSN: 1093-5266