Evidence map›Paper›PMID 39503746›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2024

Chondroblastoma of the occipital bone with aneurysmal bone cyst: A rare case report.

Dexi Bi, Zihao Wang, Zhibo Dai, Shichun Yang, Gao Zeng, Ligang Wang

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Dexi BiDepartment of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Zihao WangDepartment of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Zhibo DaiDepartment of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China. zhibodai@126.com.
Shichun YangDepartment of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Gao ZengDepartment of Neurosurgery, Xuan Wu Hospital of the Capital Medical University, Beijing, 100053, China.
Ligang WangDepartment of Neurosurgery, the First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China. wangligang1982730@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChondroblastoma 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.

conclusionThis case highlights the rare presentation of occipital bone chondroblastoma and emphasizes the importance of early surgical intervention for positive outcomes in pediatric patients.

Indexed as

Bone Cysts, AneurysmalChondroblastomaOccipital BoneChildFemaleHumansMagnetic Resonance ImagingSkull NeoplasmsAneurysmal bone cystChondroblastomaOccipital bonePediatric neurosurgery

Identifiers

PMID39503746

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.