Difference between revisions of "Metaphyseal fibrous defect"

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| Micro      =
| Micro      =
| Subtypes  =
| Subtypes  =
| LMDDx      = [[giant cell tumour of bone]]
| LMDDx      = [[giant cell tumour of bone]], others
| Stains    =
| Stains    =
| IHC        =
| IHC        =
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| ClinDDx    =
| ClinDDx    =
| Tx        = none
| Tx        = none
}}
{{ Infobox external links
| Name            = {{PAGENAME}}
| EHVSC          =
| EHVSC_mult      =
| pathprotocols  =
| wikipedia      = Nonossifying fibroma
| pathoutlines    =  {{Pathologyoutlines|topic/bonemetaphysealfibrousdefect}}
| rosaicollection =
}}
}}
'''Metaphyseal fibrous defect''', abbreviated '''MFD''', is a common benign abnormality of the [[metaphysis]], classically seen in children and young adults.
'''Metaphyseal fibrous defect''', abbreviated '''MFD''', is a common benign abnormality of the [[metaphysis]], classically seen in children and young adults.
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*Often small lesions discovered as an radiographic incidentaloma.
*Often small lesions discovered as an radiographic incidentaloma.
*Rarely seen as a pathologic specimen (should not be biopsied).
*Rarely seen as a pathologic specimen (should not be biopsied).
*May be seen in the context of ''Jaffe-Campanacci syndrome''.<ref>URL: [http://www.bonetumor.org/plasma-cell-tumors/jaffe-campanacci-syndrome http://www.bonetumor.org/plasma-cell-tumors/jaffe-campanacci-syndrome]. Accessed on: October 14, 2014.</ref>
*May be seen in the context of ''Jaffe-Campanacci syndrome'' which may be a presentation of Neurofibromatosis Type 1.<ref>URL: [http://www.bonetumor.org/plasma-cell-tumors/jaffe-campanacci-syndrome http://www.bonetumor.org/plasma-cell-tumors/jaffe-campanacci-syndrome]. Accessed on: October 14, 2014.</ref><ref>{{Cite journal  | last1 = Stewart | first1 = DR. | last2 = Brems | first2 = H. | last3 = Gomes | first3 = AG. | last4 = Ruppert | first4 = SL. | last5 = Callens | first5 = T. | last6 = Williams | first6 = J. | last7 = Claes | first7 = K. | last8 = Bober | first8 = MB. | last9 = Hachen | first9 = R. | title = Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder. | journal = Genet Med | volume = 16 | issue = 6 | pages = 448-59 | month = Jun | year = 2014 | doi = 10.1038/gim.2013.163 | PMID = 24232412 }}
</ref>
*Radiographic diagnosis.


Clinical history:
Clinical history:
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*Pathologic fracture.
*Pathologic fracture.


Prognosis:
Treatment:
*Ideally should not be biopsied.
*None (spontaneously resolve by ossification).
*Radiographically characteristic and benign.
**Diagnosis is part of the ''skeletal do not touch list''.<ref>URL: [http://radiopaedia.org/articles/skeletal-do-not-touch-lesions-1 http://radiopaedia.org/articles/skeletal-do-not-touch-lesions-1]. Accessed on: October 14, 2014.</ref>
*Ideally should not be treated or even biopsied.
 
*Spontaneously resolve by ossification.
Notes:
*May resolve into a 'bone island'.
*May resolve into a ''bone island''.
 
Clinical DDx:
*''FOG MACHINES'' acronym for radiographically lytic bone lesions.<ref>URL: [http://radiopaedia.org/articles/lytic-bone-lesion-mnemonic http://radiopaedia.org/articles/lytic-bone-lesion-mnemonic]. Accessed on: October 14, 2014.</ref>
 
==Gross==
*Firm, granular, brown to yellow to red.


==Site==
Site:
*Metaphysis of distal femur or proximal tibia (80%).
*[[Metaphysis]] of distal femur or proximal tibia (80%).
*Cortical.
*Cortical.
*[[Metaphysis]].
*Metaphysis.
*Long bones.
*Long bones.
*Eccentric location.
*Eccentric location.


==Gross==
===Radiology===
*Firm, granular, brown to yellow to red.
*Sharply demarcated, lucent, loculated, meta-diaphyseal lesion.
*Surrounded by a rim of sclerotic bone.
 
<gallery>
Image:NOF 1.jpg|Nonossifying fibroma. (WC)
</gallery>


==Microscopic==
==Microscopic==
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DDx (microscopic):
DDx (microscopic):
*[[Giant cell tumour of bone]] - [[epiphysis|epiphyseal]] location, occurs in adults.
*[[Giant cell tumour of bone]] - [[epiphysis|epiphyseal]] location, occurs in adults.
 
*Other [[giant cell lesions]] of bone.
==Relevant Diagnostic Groups==
*[[Spindle cell lesion]]s of bone.
*Clinical
**FOG MACHINES - acronym for radiographically lytic bone lesions <ref>URL: [http://radiopaedia.org/articles/lytic-bone-lesion-mnemonic http://radiopaedia.org/articles/lytic-bone-lesion-mnemonic]. Accessed on: October 14, 2014.</ref>
**'Skeletal do not touch list' <ref>URL: [http://radiopaedia.org/articles/skeletal-do-not-touch-lesions-1 http://radiopaedia.org/articles/skeletal-do-not-touch-lesions-1]. Accessed on: October 14, 2014.</ref>
*Pathologic
**Giant cell lesions of bone.
**Spindle cell lesions of bone.


==Images==
==Images==
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==IHC==
==IHC==
*Not relevant
*Not relevant.


==Molecular==
==Molecular==
*Not relevant
*Not relevant.
 
==Radiographic findings==
Sharply demarcated, lucent, loculated, meta-diaphyseal lesion surrounded by a rim of sclerotic bone


==Sign out==
==Sign out==
<pre>
<pre>
BONE, CURETTAGE: METAPHYSEAL FIBROUS DEFECT / NONOSSIFYING FIBROMA.
BONE, CURETTAGE:  
- METAPHYSEAL FIBROUS DEFECT / NONOSSIFYING FIBROMA.
</pre>
</pre>


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==External links==
==External links==
*http://njms2.umdnj.edu/tutorweb/case8.htm
*[http://njms2.umdnj.edu/tutorweb/case8.htm A case of MFD (umdnj.edu)].
*http://www.pathologyoutlines.com/topic/bonemetaphysealfibrousdefect.html
*[http://radiopaedia.org/articles/fibrous-cortical-defect Fibrous cortical defect (radiopaedia.org)].
*http://radiopaedia.org/articles/fibrous-cortical-defect
*[http://radiopaedia.org/articles/non-ossifying-fibroma-1 Non-ossifying fibroma (radiopaedia.org)].
*http://radiopaedia.org/articles/non-ossifying-fibroma-1


[[Category:Diagnosis]]
[[Category:Diagnosis]]
[[Category:Bone]]
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