Chondroma x ray: Difference between revisions

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{{Chondroma}}
{{Chondroma}}
{{CMG}}{{AE}} {{STM}}
{{CMG}}; {{AE}} {{Rohan}}, {{F.K}}, {{STM}}


==Overview==
==Overview==
On x rays, enchondroma is characterized by [[lytic]] lesions that contain calcified chondroid [[matrix]].<ref name=ma>Enchondroma. Wikipedia. https://en.wikipedia.org/wiki/Enchondroma Accessed on December 22, 2015.</ref> On x rays, periosteal chondroma is characterized by matrix [[calcification]] with ring and arc pattern and saucerisation of the adjacent bony cortex with a sclerotic [[periosteal reaction]].<ref name=jn>Juxta cortical chondroma. Radiopedia. http://radiopaedia.org/articles/juxta-cortical-chondroma Accessed on December 22, 2015</ref>
Findings on an x-ray suggestive of chondroma include well-defined or sclerotic border, sharp zone of transition, confinement by natural barriers, lack of destruction of the [[cortex]] and lack of extension into the [[soft tissue]].


==X Ray Findings==
==X Ray Findings==
*An x-ray may be helpful in the diagnosis of chondroma. Findings on an x-ray suggestive of chondroma include:
*X-ray may be helpful in the diagnosis of chondroma. Findings on an x-ray suggestive of chondroma include:<ref name="pmid18328980">{{cite journal |vauthors=Pannier S, Legeai-Mallet L |title=Hereditary multiple exostoses and enchondromatosis |journal=Best Pract Res Clin Rheumatol |volume=22 |issue=1 |pages=45–54 |date=March 2008 |pmid=18328980 |doi=10.1016/j.berh.2007.12.004 |url=}}</ref><ref name="pmid16995932">{{cite journal |vauthors=Silve C, Jüppner H |title=Ollier disease |journal=Orphanet J Rare Dis |volume=1 |issue= |pages=37 |date=September 2006 |pmid=16995932 |pmc=1592482 |doi=10.1186/1750-1172-1-37 |url=}}</ref><ref name="pmid16624212">{{cite journal |vauthors=Gajewski DA, Burnette JB, Murphey MD, Temple HT |title=Differentiating clinical and radiographic features of enchondroma and secondary chondrosarcoma in the foot |journal=Foot Ankle Int |volume=27 |issue=4 |pages=240–4 |date=April 2006 |pmid=16624212 |doi=10.1177/107110070602700403 |url=}}</ref><ref name="pmid9308471">{{cite journal |vauthors=Geirnaerdt MJ, Hermans J, Bloem JL, Kroon HM, Pope TL, Taminiau AH, Hogendoorn PC |title=Usefulness of radiography in differentiating enchondroma from central grade 1 chondrosarcoma |journal=AJR Am J Roentgenol |volume=169 |issue=4 |pages=1097–104 |date=October 1997 |pmid=9308471 |doi=10.2214/ajr.169.4.9308471 |url=}}</ref><ref name="pmid15116654">{{cite journal |vauthors=Weiner SD |title=Enchondroma and chondrosarcoma of bone: clinical, radiologic, and histologic differentiation |journal=Instr Course Lect |volume=53 |issue= |pages=645–9 |date=2004 |pmid=15116654 |doi= |url=}}</ref><ref name="pmid23955368">{{cite journal |vauthors=Miller SF |title=Imaging features of juxtacortical chondroma in children |journal=Pediatr Radiol |volume=44 |issue=1 |pages=56–63 |date=January 2014 |pmid=23955368 |doi=10.1007/s00247-013-2770-6 |url=}}</ref>
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[[File:Xray chondroma.gif|300px|thumb|X-ray of knee showing chondroma.[https://radiopaedia.org/cases/periosteal-chondroma-1?lang=us Source: Case courtesy of Dr Brian Gilcrease-Garcia, Radiopaedia.org, rID: 56933]]]
|}
**Well-defined or sclerotic border
**Well-defined or sclerotic border
**Sharp zone of transition
**Sharp zone of transition
**Small size or multiple lesions
**Small size or multiple lesions
**Confinement by natural barriers  
**Confinement by natural barriers  
**Lack of destruction of the cortex
**Lack of destruction of the [[cortex]]
**Lack of extension into the soft tissue
**Lack of extension into the soft tissue
*Following x-ray findings are suggestive of more aggresive lesion:
*Following x-ray findings are suggestive of more aggresive lesion:
**Poor definition
**Poor definition
**Cortical destruction ("moth-eaten" or permeative pattern)
**Cortical destruction ("moth-eaten" or permeative pattern)
**Spiculated or interrupted periosteal reaction
**Spiculated or interrupted [[periosteal reaction]]
**Extension into the soft tissue
**Extension into the soft tissue
**Large size
**Large size


*'''Enchondroma'''
=== '''Enchondroma''' ===
**Oval, well-circumscribed, central lucent lesion, with or without matrix calcifications
:*Oval, well-circumscribed, central lucent lesion, with or without matrix calcifications
**May be expansion of the surrounding cortex, especially when the lesion is in the hand or foot
:*May be expansion of the surrounding [[cortex]], especially when the lesion is in the hand or foot
*'''Periosteal chondroma'''
 
**Small, scalloped, radiolucent lesions on the outer surface of the cortex in the metaphysis or diaphysis  
=== '''Periosteal chondroma''' ===
**Rim of sclerotic bone
:*Small, scalloped, radiolucent lesions on the outer surface of the cortex in the [[metaphysis]] or [[diaphysis]]
**Calcification
:*Rim of sclerotic bone
:*Calcification


==References==
==References==

Latest revision as of 18:08, 24 January 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rohan A. Bhimani, M.B.B.S., D.N.B., M.Ch.[2], Farima Kahe M.D. [3], Soujanya Thummathati, MBBS [4]

Overview

Findings on an x-ray suggestive of chondroma include well-defined or sclerotic border, sharp zone of transition, confinement by natural barriers, lack of destruction of the cortex and lack of extension into the soft tissue.

X Ray Findings

  • X-ray may be helpful in the diagnosis of chondroma. Findings on an x-ray suggestive of chondroma include:[1][2][3][4][5][6]
X-ray of knee showing chondroma.Source: Case courtesy of Dr Brian Gilcrease-Garcia, Radiopaedia.org, rID: 56933
    • Well-defined or sclerotic border
    • Sharp zone of transition
    • Small size or multiple lesions
    • Confinement by natural barriers
    • Lack of destruction of the cortex
    • Lack of extension into the soft tissue
  • Following x-ray findings are suggestive of more aggresive lesion:
    • Poor definition
    • Cortical destruction ("moth-eaten" or permeative pattern)
    • Spiculated or interrupted periosteal reaction
    • Extension into the soft tissue
    • Large size

Enchondroma

  • Oval, well-circumscribed, central lucent lesion, with or without matrix calcifications
  • May be expansion of the surrounding cortex, especially when the lesion is in the hand or foot

Periosteal chondroma

  • Small, scalloped, radiolucent lesions on the outer surface of the cortex in the metaphysis or diaphysis
  • Rim of sclerotic bone
  • Calcification

References

  1. Pannier S, Legeai-Mallet L (March 2008). "Hereditary multiple exostoses and enchondromatosis". Best Pract Res Clin Rheumatol. 22 (1): 45–54. doi:10.1016/j.berh.2007.12.004. PMID 18328980.
  2. Silve C, Jüppner H (September 2006). "Ollier disease". Orphanet J Rare Dis. 1: 37. doi:10.1186/1750-1172-1-37. PMC 1592482. PMID 16995932.
  3. Gajewski DA, Burnette JB, Murphey MD, Temple HT (April 2006). "Differentiating clinical and radiographic features of enchondroma and secondary chondrosarcoma in the foot". Foot Ankle Int. 27 (4): 240–4. doi:10.1177/107110070602700403. PMID 16624212.
  4. Geirnaerdt MJ, Hermans J, Bloem JL, Kroon HM, Pope TL, Taminiau AH, Hogendoorn PC (October 1997). "Usefulness of radiography in differentiating enchondroma from central grade 1 chondrosarcoma". AJR Am J Roentgenol. 169 (4): 1097–104. doi:10.2214/ajr.169.4.9308471. PMID 9308471.
  5. Weiner SD (2004). "Enchondroma and chondrosarcoma of bone: clinical, radiologic, and histologic differentiation". Instr Course Lect. 53: 645–9. PMID 15116654.
  6. Miller SF (January 2014). "Imaging features of juxtacortical chondroma in children". Pediatr Radiol. 44 (1): 56–63. doi:10.1007/s00247-013-2770-6. PMID 23955368.


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