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Temporal bone chondroblastoma: Imaging characteristics with pathologic correlation

Authors
Park, Sun-WonKim, Ji-HoonPark, Ji HoonMoon, Kyung ChulPaeng, Jin ChulChoi, Byung SeLee, YounghenKim, Jae HyoungYoo, Roh-EulKang, Koung MiKim, Soo ChinChoi, Seung HongYun, Tae JinSohn, Chul Ho
Issue Date
Nov-2017
Publisher
WILEY
Keywords
chondroblastoma; CT; fluorodeoxyglucose (FDG); MRI; positron emission tomography (PET); temporal bone
Citation
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, v.39, no.11, pp.2171 - 2179
Indexed
SCIE
SCOPUS
Journal Title
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
Volume
39
Number
11
Start Page
2171
End Page
2179
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/81727
DOI
10.1002/hed.24880
ISSN
1043-3074
Abstract
Background: Chondroblastoma commonly involves the temporal bone in the craniofacial region, but its imaging features have not been elucidated. This study aimed to describe the imaging features of temporal bone chondroblastoma with their pathologic correlation. Methods: Radiopathologic correlation was performed in 5 patients with temporal bone chondroblastoma from our database and in 11 patients identified through a PubMed search. Results: The cases of temporal bone chondroblastoma commonly involve the squamous part, temporal and infratemporal fossae, temporomandibular joint, and tympanic cavity, with the following features: high attenuation with calcification; heterogeneity; low signal intensity on T2-weighted imaging with enhancement; a smooth interface to the brain; and strong hypermetabolism on fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT. The heterogeneous low signal intensity on T2-weighted imaging was correlated with various histopathologic components, including calcification and hemosiderin deposition. Conclusion: Temporal bone chondroblastoma usually forms as an expansile, heterogeneous, hypermetabolic mass in the middle cranial fossa, frequently with low signal intensity on T2-weighted imaging, reflecting various degrees of calcification and hemosiderin deposition.
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