Case Presentation: Hereditary Multiple Exostosis in a Pediatric Patient
Abstract: Hereditary Multiple Exostosis (HME) is a rare, autosomal dominant disorder marked by the development of multiple osteochondromas, primarily at the metaphyseal regions of long bones. The disorder may result in growth disturbances, deformity, and in rare cases, malignant transformation. This case involves an 8-year-old male presenting with gradually enlarging, painless swellings and forearm deformity. Clinical evaluation, radiographic findings, and surgical considerations are discussed. The case emphasizes the need for early diagnosis, routine surveillance, and timely intervention to prevent long-term complications.
Keywords: Hereditary Multiple Exostosis, Osteochondroma, Pediatric Orthopedics, Forearm Deformity, Genetic Skeletal Disorder, Surgical Excision
How to Cite?: Prabha S., Yositha, "Case Presentation: Hereditary Multiple Exostosis in a Pediatric Patient", Volume 14 Issue 4, April 2025, International Journal of Science and Research (IJSR), Pages: 1855-1856, https://www.ijsr.net/getabstract.php?paperid=MR25421195910, DOI: https://dx.doi.org/10.21275/MR25421195910