Difference between revisions of "Osteofibrous dysplasia"
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{{ Infobox diagnosis | {{ Infobox diagnosis | ||
| Name = {{ | | Name = {{PAGENAME}} | ||
| Image = | | Image = | ||
| Width = | | Width = | ||
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| Micro = | | Micro = | ||
| Subtypes = | | Subtypes = | ||
| LMDDx = | | LMDDx = [[adamantinoma]], OFD-like [[adamantinoma]], [[fibrous dysplasia]] | ||
| Stains = | | Stains = | ||
| IHC = | | IHC = | ||
| EM = | | EM = | ||
| Molecular = | | Molecular = clonal chromosomal abnormalities | ||
| IF = | | IF = | ||
| Gross = | | Gross = | ||
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| Syndromes = | | Syndromes = | ||
| Clinicalhx = | | Clinicalhx = | ||
| Signs = | | Signs = tibial swelling, bowing | ||
| Symptoms = | | Symptoms = | ||
| Prevalence = | | Prevalence = rare | ||
| Bloodwork = | | Bloodwork = | ||
| Rads = | | Rads = lytic bone lesion | ||
| Endoscopy = | | Endoscopy = | ||
| Prognosis = | | Prognosis = self limited | ||
| Other = | | Other = may be related to adamantinoma | ||
| ClinDDx = | | ClinDDx = [[adamantinoma]], [[fibrous dysplasia]], [[metaphyseal fibrous defect]], [[osteosarcoma]] | ||
| Tx = | | Tx = observation | ||
}} | }} | ||
'''Osteofibrous dysplasia''' is a rare benign condition that afflicits the long bones.<ref name=pmid1563159>{{Cite journal | last1 = Wang | first1 = JW. | last2 = Shih | first2 = CH. | last3 = Chen | first3 = WJ. | title = Osteofibrous dysplasia (ossifying fibroma of long bones). A report of four cases and review of the literature. | journal = Clin Orthop Relat Res | volume = | issue = 278 | pages = 235-43 | month = May | year = 1992 | doi = | PMID = 1563159 }}</ref> | |||
It is also known as '''ossifying fibroma of long bones'''<ref name=pmid1563159/> and '''congenital osteitis fibrosa'''. | |||
* | ==General== | ||
* | Features:<ref>{{Cite web | last = | first = | title = http://www.smbs.buffalo.edu/ortho/tumorarticles/osteofibrousdysplasiaandadamantinoma.pdf | url = http://www.smbs.buffalo.edu/ortho/tumorarticles/osteofibrousdysplasiaandadamantinoma.pdf | publisher = | date = | accessdate = 18 October 2014 }}</ref> | ||
*Benign fibro-osseous lesion. | |||
*Rare.<ref name=pmid1563159/> | |||
Alternate names. | |||
* | *Congenital osteitis fibrosa. | ||
Location: | |||
* | *Cortex of the tibial diaphysis | ||
Pathophysiology: | |||
*May be either a clonal neoplastic lesion or a developmental dysplasia. | |||
* | *May be related to adamantinoma | ||
* | |||
Presentation: | |||
* | *Lower leg swelling. | ||
* | *Pain. | ||
* | *Tibial bowing | ||
Radiology: | |||
* | *Intracortical lytic lesion. | ||
* | *Surrounding zone of sclerosis. | ||
* | *Seldom progresses radiologically. | ||
* | Clinical DDX: | ||
** | *[[Adamantinoma]] - usually older (teens-twenties), may have soft tissue extension. | ||
*[[Metaphyseal fibrous defect]] - metaphyseal location. | |||
*[[Fibrous dysplasia]]. | |||
*Population | Prognosis: | ||
*Self limited | |||
Population: | |||
*Children. | |||
*First 2 decades of life. | |||
*Median 9.5 years. | |||
==Gross== | ==Gross== | ||
Line 71: | Line 76: | ||
The lesion has a zonal architecture with a center of immature bone surrounded by more mature lamellar bone. The central spicules of woven bony trabeculae are lined by a layer of osteoblasts. The backgound is a loose and storiform fibrous tissue. | The lesion has a zonal architecture with a center of immature bone surrounded by more mature lamellar bone. The central spicules of woven bony trabeculae are lined by a layer of osteoblasts. The backgound is a loose and storiform fibrous tissue. | ||
Notes: | |||
* | *The diagnosis depends on the ratio of fibrous to epithelial tissue which can vary within each particular tumour. | ||
** | **Due to the above ample tissue is required for accurate histologic diagnosis. | ||
*Current discussion regarding the definition of an OFD-like adamantinoma. | |||
**As of 2010, WHO requires absence of keratin-positive cells for OFD. | |||
**Some accept as OFD lesions with scattered isolated keratin positive spindled cells. | |||
**Gray zone and varying interpretations of the boundry of OFD, OFD-like adamantinoma and adamantinoma. | |||
** | |||
* | DDx: | ||
** | *[[Adamantinoma]] - epithelial elements are prominent and atypical. | ||
*OFD-like [[adamantinoma]] - see below. | |||
*[[Fibrous dysplasia]] - bony trabeculae lack osteoblastic rimming, not zonal. | |||
==Images== | ===Images=== | ||
*OFD-Tumor Library| [http://www.tumorlibrary.com/case/images/1326.jpg] | *OFD-Tumor Library| [http://www.tumorlibrary.com/case/images/1326.jpg] | ||
*OFD-Pathology Outlines| [http://pathologyoutlines.com/wick/osteofibrous%20dysplasia%20(Campanacci%20disease)%20micro002.jpg] | *OFD-Pathology Outlines| [http://pathologyoutlines.com/wick/osteofibrous%20dysplasia%20(Campanacci%20disease)%20micro002.jpg] | ||
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==Stains== | ==Stains== | ||
Not relevant | *Not relevant | ||
==IHC== | ==IHC== | ||
Keratin positive isolated cells accepted by some. | *Keratin positive - isolated cells accepted by some. | ||
==Molecular== | ==Molecular== | ||
Clonal chromosomal abnormalities | Clonal chromosomal abnormalities | ||
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==Sign out== | ==Sign out== | ||
BONE | <pre> | ||
BONE, CURRETTAGE: | |||
- OSTEOFIBROUS DYSPLASIA. | |||
</pre> | |||
==See also== | ==See also== | ||
*Tumor Library |http://www.tumorlibrary.com/case/list.jsp?case_id=95 | *Tumor Library |[http://www.tumorlibrary.com/case/list.jsp?case_id=95] | ||
*Sarcoma Images |http://www.sarcomaimages.com/sub.php?v=812-sample-case&p=osteofibrous-dysplasia | *Sarcoma Images |[http://www.sarcomaimages.com/sub.php?v=812-sample-case&p=osteofibrous-dysplasia] | ||
==References== | ==References== |
Latest revision as of 00:17, 2 February 2015
Osteofibrous dysplasia | |
---|---|
Diagnosis in short | |
LM DDx | adamantinoma, OFD-like adamantinoma, fibrous dysplasia |
Molecular | clonal chromosomal abnormalities |
Signs | tibial swelling, bowing |
Prevalence | rare |
Radiology | lytic bone lesion |
Prognosis | self limited |
Other | may be related to adamantinoma |
Clin. DDx | adamantinoma, fibrous dysplasia, metaphyseal fibrous defect, osteosarcoma |
Treatment | observation |
Osteofibrous dysplasia is a rare benign condition that afflicits the long bones.[1]
It is also known as ossifying fibroma of long bones[1] and congenital osteitis fibrosa.
General
Features:[2]
- Benign fibro-osseous lesion.
- Rare.[1]
Alternate names.
- Congenital osteitis fibrosa.
Location:
- Cortex of the tibial diaphysis
Pathophysiology:
- May be either a clonal neoplastic lesion or a developmental dysplasia.
- May be related to adamantinoma
Presentation:
- Lower leg swelling.
- Pain.
- Tibial bowing
Radiology:
- Intracortical lytic lesion.
- Surrounding zone of sclerosis.
- Seldom progresses radiologically.
Clinical DDX:
- Adamantinoma - usually older (teens-twenties), may have soft tissue extension.
- Metaphyseal fibrous defect - metaphyseal location.
- Fibrous dysplasia.
Prognosis:
- Self limited
Population:
- Children.
- First 2 decades of life.
- Median 9.5 years.
Gross
Microscopic
The lesion has a zonal architecture with a center of immature bone surrounded by more mature lamellar bone. The central spicules of woven bony trabeculae are lined by a layer of osteoblasts. The backgound is a loose and storiform fibrous tissue.
Notes:
- The diagnosis depends on the ratio of fibrous to epithelial tissue which can vary within each particular tumour.
- Due to the above ample tissue is required for accurate histologic diagnosis.
- Current discussion regarding the definition of an OFD-like adamantinoma.
- As of 2010, WHO requires absence of keratin-positive cells for OFD.
- Some accept as OFD lesions with scattered isolated keratin positive spindled cells.
- Gray zone and varying interpretations of the boundry of OFD, OFD-like adamantinoma and adamantinoma.
DDx:
- Adamantinoma - epithelial elements are prominent and atypical.
- OFD-like adamantinoma - see below.
- Fibrous dysplasia - bony trabeculae lack osteoblastic rimming, not zonal.
Images
- OFD-Tumor Library| [1]
- OFD-Pathology Outlines| [2]
- OFD-Pathology Outlines | [3]
- OFD-Pathology Outlines | [4]
- OFD-Sarcoma Images | [5]
- OFD-Sarcoma Images | [6]
- OFD-Sarcoma Images | [7]
- OFD-Sarcoma Images | [8]
Stains
- Not relevant
IHC
- Keratin positive - isolated cells accepted by some.
Molecular
Clonal chromosomal abnormalities
- Trisomies of chromosomes 7, 8, 12,21, and/or 22
Sign out
BONE, CURRETTAGE: - OSTEOFIBROUS DYSPLASIA.
See also
References
- ↑ 1.0 1.1 1.2 Wang, JW.; Shih, CH.; Chen, WJ. (May 1992). "Osteofibrous dysplasia (ossifying fibroma of long bones). A report of four cases and review of the literature.". Clin Orthop Relat Res (278): 235-43. PMID 1563159.
- ↑ "http://www.smbs.buffalo.edu/ortho/tumorarticles/osteofibrousdysplasiaandadamantinoma.pdf". http://www.smbs.buffalo.edu/ortho/tumorarticles/osteofibrousdysplasiaandadamantinoma.pdf. Retrieved 18 October 2014.