Difference between revisions of "Nodular fasciitis"

Jump to navigation Jump to search
936 bytes added ,  03:17, 29 September 2013
tweak
(tweak)
Line 12: Line 12:
| Molecular  = t(15;15) ?
| Molecular  = t(15;15) ?
| IF        =
| IF        =
| Gross      =
| Gross      = usu. upper extremity ~45% of cases
| Grossing  =
| Grossing  =
| Site      = [[soft tissue lesions|soft tissue]] - [[fibroblastic/myofibroblastic tumours]]
| Site      = [[soft tissue lesions|soft tissue]] - [[fibroblastic/myofibroblastic tumours]]
Line 31: Line 31:
==General==
==General==
*Benign.
*Benign.
*All age groups.
*All age groups - though typically 20-40 years old.
*Associated with trauma.
*Associated with trauma.
*Rapid growth - clinically concerning for malignancy.<ref name=pmid14569327>{{Cite journal  | last1 = Chi | first1 = CC. | last2 = Kuo | first2 = TT. | last3 = Wang | first3 = SH. | title = Nodular fasciitis: clinical characteristics and preoperative diagnosis. | journal = J Formos Med Assoc | volume = 102 | issue = 8 | pages = 586-9 | month = Aug | year = 2003 | doi =  | PMID = 14569327 }}</ref>
*Rapid growth - clinically concerning for malignancy.<ref name=pmid14569327>{{Cite journal  | last1 = Chi | first1 = CC. | last2 = Kuo | first2 = TT. | last3 = Wang | first3 = SH. | title = Nodular fasciitis: clinical characteristics and preoperative diagnosis. | journal = J Formos Med Assoc | volume = 102 | issue = 8 | pages = 586-9 | month = Aug | year = 2003 | doi =  | PMID = 14569327 }}</ref>
*Commonly misdiagnosed as malignant.<ref name=pmid17235006 >{{Cite journal  | last1 = Dinauer | first1 = PA. | last2 = Brixey | first2 = CJ. | last3 = Moncur | first3 = JT. | last4 = Fanburg-Smith | first4 = JC. | last5 = Murphey | first5 = MD. | title = Pathologic and MR imaging features of benign fibrous soft-tissue tumors in adults. | journal = Radiographics | volume = 27 | issue = 1 | pages = 173-87 | month =  | year =  | doi = 10.1148/rg.271065065 | PMID = 17235006 | URL = http://radiographics.rsna.org/content/27/1/173.long }}</ref>
Subtypes - location:<ref name=pmid17235006/>
*Subcutaneous.
*Intramuscular.
*Fascial
*Dermal - rare.
*Intravascular - rare.
==Gross==
*Usually upper extremity ~45% of cases.<ref name=pmid17235006/>
**Other locations in order: trunk (~20%), head and neck (~20%), and lower extremities (~15%).


==Microscopic==
==Microscopic==
Line 57: Line 69:


DDx:<ref>URL: [http://www.mckeedermpath.com/SPOT%20DIAGNOSIS%20CASE%20268.html http://www.mckeedermpath.com/SPOT%20DIAGNOSIS%20CASE%20268.html]. Accessed on: 11 November 2011.</ref>
DDx:<ref>URL: [http://www.mckeedermpath.com/SPOT%20DIAGNOSIS%20CASE%20268.html http://www.mckeedermpath.com/SPOT%20DIAGNOSIS%20CASE%20268.html]. Accessed on: 11 November 2011.</ref>
*Myxoid [[DFSP]].
*Myxoid [[dermatofibrosarcoma protuberans]].
*Cellular [[dermatofibroma]].
*Cellular [[dermatofibroma]].
*[[Desmoid-type fibromatosis]].
*[[Desmoid-type fibromatosis]].
48,868

edits

Navigation menu