Chondroblastoma of the occipital bone with aneurysmal bone cyst: A rare case report.
Autor: | Bi D; Department of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China., Wang Z; Department of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China., Dai Z; Department of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China. zhibodai@126.com., Yang S; Department of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China., Zeng G; Department of Neurosurgery, Xuan Wu Hospital of the Capital Medical University, Beijing, 100053, China., Wang L; Department of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China. wangligang1982730@163.com. |
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Jazyk: | angličtina |
Zdroj: | Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery [Childs Nerv Syst] 2024 Dec; Vol. 40 (12), pp. 4323-4327. Date of Electronic Publication: 2024 Nov 06. |
DOI: | 10.1007/s00381-024-06632-0 |
Abstrakt: | Background: Chondroblastoma is a rare, benign bone tumor originating from immature chondrocytes, typically found in the epiphyseal plates of long bones. Its occurrence in the skull, particularly the occipital bone, is extremely rare. Case Presentation: We report a 10-year-old girl presenting with paroxysmal dizziness, occipital pain, and a palpable mass. Imaging studies revealed an osteolytic lesion in the occipital bone with a multiloculated appearance, indicating a concomitant aneurysmal bone cyst. The patient underwent craniotomy with complete tumor excision. Postoperative follow-up showed no neurological deficits or complications and MRI confirmed no recurrence. Conclusion: This case highlights the rare presentation of occipital bone chondroblastoma and emphasizes the importance of early surgical intervention for positive outcomes in pediatric patients. Competing Interests: Declarations. Competing interests: The authors declare no competing interests. (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) |
Databáze: | MEDLINE |
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