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MR Findings of the Osteofibrous Dysplasia

OBJECTIVE: The aim of this study was to describe MR findings of osteofibrous dysplasia. MATERIALS AND METHODS: MR images of 24 pathologically proven osteofibrous dysplasia cases were retrospectively analyzed for a signal intensity of the lesion, presence of intralesional fat signal, internal hypoint...

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Autores principales: Jung, Joon-Yong, Jee, Won-Hee, Hong, Sung Hwan, Kang, Heung Sik, Chung, Hye Won, Ryu, Kyung-Nam, Kim, Jee-Young, Im, Soo-A, Park, Jeong-Mi, Sung, Mi-Sook, Lee, Yeon-Soo, Hong, Suk-Joo, Jung, Chan-Kwon, Chung, Yang-Guk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Radiology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909842/
https://www.ncbi.nlm.nih.gov/pubmed/24497800
http://dx.doi.org/10.3348/kjr.2014.15.1.114
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author Jung, Joon-Yong
Jee, Won-Hee
Hong, Sung Hwan
Kang, Heung Sik
Chung, Hye Won
Ryu, Kyung-Nam
Kim, Jee-Young
Im, Soo-A
Park, Jeong-Mi
Sung, Mi-Sook
Lee, Yeon-Soo
Hong, Suk-Joo
Jung, Chan-Kwon
Chung, Yang-Guk
author_facet Jung, Joon-Yong
Jee, Won-Hee
Hong, Sung Hwan
Kang, Heung Sik
Chung, Hye Won
Ryu, Kyung-Nam
Kim, Jee-Young
Im, Soo-A
Park, Jeong-Mi
Sung, Mi-Sook
Lee, Yeon-Soo
Hong, Suk-Joo
Jung, Chan-Kwon
Chung, Yang-Guk
author_sort Jung, Joon-Yong
collection PubMed
description OBJECTIVE: The aim of this study was to describe MR findings of osteofibrous dysplasia. MATERIALS AND METHODS: MR images of 24 pathologically proven osteofibrous dysplasia cases were retrospectively analyzed for a signal intensity of the lesion, presence of intralesional fat signal, internal hypointense band, multilocular appearance, cortical expansion, intramedullary extension, cystic area, cortical breakage and extraosseous extension, abnormal signal from the adjacent bone marrow and soft tissue and patterns of contrast enhancement. RESULTS: All cases of osteofibrous dysplasia exhibited intermediate signal intensity on T1-weighted images. On T2-weighted images, 20 and 4 cases exhibited heterogeneously intermediate and high signal intensity, respectively. Intralesional fat was identified in 12% of the cases. Internal low-signal bands and multilocular appearance were observed in 91%. Cortical expansion was present in 58%. Intramedullary extension was present in all cases, and an entire intramedullary replacement was observed in 33%. Cortical breakage (n = 3) and extraosseous mass formation (n = 1) were observed in cases with pathologic fractures only. A cystic area was observed in one case. Among 21 cases without a pathologic fracture, abnormal signal intensity in the surrounding bone marrow and adjacent soft tissue was observed in 43% and 48%, respectively. All cases exhibited diffuse contrast enhancement. CONCLUSION: Osteofibrous dysplasia exhibited diverse imaging features ranging from lesions confined to the cortex to more aggressive lesions with complete intramedullary involvement or perilesional marrow edema.
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spelling pubmed-39098422014-02-04 MR Findings of the Osteofibrous Dysplasia Jung, Joon-Yong Jee, Won-Hee Hong, Sung Hwan Kang, Heung Sik Chung, Hye Won Ryu, Kyung-Nam Kim, Jee-Young Im, Soo-A Park, Jeong-Mi Sung, Mi-Sook Lee, Yeon-Soo Hong, Suk-Joo Jung, Chan-Kwon Chung, Yang-Guk Korean J Radiol Musculoskeletal Imaging OBJECTIVE: The aim of this study was to describe MR findings of osteofibrous dysplasia. MATERIALS AND METHODS: MR images of 24 pathologically proven osteofibrous dysplasia cases were retrospectively analyzed for a signal intensity of the lesion, presence of intralesional fat signal, internal hypointense band, multilocular appearance, cortical expansion, intramedullary extension, cystic area, cortical breakage and extraosseous extension, abnormal signal from the adjacent bone marrow and soft tissue and patterns of contrast enhancement. RESULTS: All cases of osteofibrous dysplasia exhibited intermediate signal intensity on T1-weighted images. On T2-weighted images, 20 and 4 cases exhibited heterogeneously intermediate and high signal intensity, respectively. Intralesional fat was identified in 12% of the cases. Internal low-signal bands and multilocular appearance were observed in 91%. Cortical expansion was present in 58%. Intramedullary extension was present in all cases, and an entire intramedullary replacement was observed in 33%. Cortical breakage (n = 3) and extraosseous mass formation (n = 1) were observed in cases with pathologic fractures only. A cystic area was observed in one case. Among 21 cases without a pathologic fracture, abnormal signal intensity in the surrounding bone marrow and adjacent soft tissue was observed in 43% and 48%, respectively. All cases exhibited diffuse contrast enhancement. CONCLUSION: Osteofibrous dysplasia exhibited diverse imaging features ranging from lesions confined to the cortex to more aggressive lesions with complete intramedullary involvement or perilesional marrow edema. The Korean Society of Radiology 2014 2014-01-08 /pmc/articles/PMC3909842/ /pubmed/24497800 http://dx.doi.org/10.3348/kjr.2014.15.1.114 Text en Copyright © 2014 The Korean Society of Radiology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Musculoskeletal Imaging
Jung, Joon-Yong
Jee, Won-Hee
Hong, Sung Hwan
Kang, Heung Sik
Chung, Hye Won
Ryu, Kyung-Nam
Kim, Jee-Young
Im, Soo-A
Park, Jeong-Mi
Sung, Mi-Sook
Lee, Yeon-Soo
Hong, Suk-Joo
Jung, Chan-Kwon
Chung, Yang-Guk
MR Findings of the Osteofibrous Dysplasia
title MR Findings of the Osteofibrous Dysplasia
title_full MR Findings of the Osteofibrous Dysplasia
title_fullStr MR Findings of the Osteofibrous Dysplasia
title_full_unstemmed MR Findings of the Osteofibrous Dysplasia
title_short MR Findings of the Osteofibrous Dysplasia
title_sort mr findings of the osteofibrous dysplasia
topic Musculoskeletal Imaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909842/
https://www.ncbi.nlm.nih.gov/pubmed/24497800
http://dx.doi.org/10.3348/kjr.2014.15.1.114
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