An unusual presentation of pediatric osteoblastoma in a patient with Klippel-Trenaunay-Weber syndrome: case report
Author:
Affiliation:
1. Department of Neurosurgery, Walter Reed National Military Medical Center, Bethesda, Maryland; and
2. Surgery, Naval Medical Center San Diego, California
3. Departments of Neurosurgery,
4. Pathology, and
Abstract
Publisher
Journal of Neurosurgery Publishing Group (JNSPG)
Subject
General Medicine
Link
https://thejns.org/downloadpdf/journals/j-neurosurg-pediatr/15/6/article-p638.xml
Reference18 articles.
1. Osteoblastoma in the Skeletally Immature
2. Osteoblastoma: A 30-year study of 99 cases
3. Management of osteoblastoma and osteoid osteoma of the spine in childhood
4. Osteoblastoma: Varied Histological Presentations with a Benign Clinical Course
5. Imprinted tumor suppressor genesARHI andPEG3 are the most frequently down-regulated in human ovarian cancers by loss of heterozygosity and promoter methylation
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1. A rare case of klippel-trenaunay syndrome presenting with chronic myeloid leukemia;The Turkish Journal of Pediatrics;2023
2. Cancer Risk in Klippel–Trenaunay Syndrome;Lymphatic Research and Biology;2019-12-01
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