Difference between revisions of "Soft tissue lesions"

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update WMSP
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==WHO classification of soft tissue lesions/tumours==
==WHO classification of soft tissue lesions/tumours==
===Morphologic grouping<ref>WMSP PP.601-3.</ref>===
===Morphologic grouping<ref name=Ref_WMSP601-3>{{Ref WMSP|601-3}}</ref>===
#Adipocytic tumours.
#Adipocytic tumours.
#Fibroblastic/myofibroblastic tumours.
#Fibroblastic/myofibroblastic tumours.
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#Tumours of uncertain differentiation.
#Tumours of uncertain differentiation.


===Biologic potential grouping<ref>WMSP PP.598-604.</ref>===
===Biologic potential grouping<ref>{{Ref WMSP|598-604}}</ref>===
#Benign.
#Benign.
#Intermediate (locally aggressive).
#Intermediate (locally aggressive).
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==Hibernoma==
==Hibernoma==
===General===
===General===
*Consists of ''brown fat'' (present in the infants to generate heat).<ref>WMSP P.605.</ref>
*Consists of ''brown fat'' (present in the infants to generate heat).<ref name=Ref_WMSP605>{{Ref WMSP|605}}</ref>
*Benign.
*Benign.
*Usually asymptomatic.<ref name=pmid19131775>{{cite journal |author=Ahmed SA, Schuller I |title=Pediatric hibernoma: a case review |journal=J. Pediatr. Hematol. Oncol. |volume=30 |issue=12 |pages=900–1 |year=2008 |month=December |pmid=19131775 |doi=10.1097/MPH.0b013e318184e6dd |url=}}</ref>
*Usually asymptomatic.<ref name=pmid19131775>{{cite journal |author=Ahmed SA, Schuller I |title=Pediatric hibernoma: a case review |journal=J. Pediatr. Hematol. Oncol. |volume=30 |issue=12 |pages=900–1 |year=2008 |month=December |pmid=19131775 |doi=10.1097/MPH.0b013e318184e6dd |url=}}</ref>
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===IHC===
===IHC===
Features:<ref>WMSP P.609.</ref><ref name=enzinger/>
Features:<ref name=Ref_WMSP609>{{Ref WMSP|609}}</ref><ref name=enzinger/>
*Vimentin +ve (usually).
*Vimentin +ve (usually).
*Desmin -ve (typical).
*Desmin -ve (typical).
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====Grading====
====Grading====
Features:<ref>WMSP P.643.</ref>
Features:<ref name=Ref_WMSP643>{{Ref WMSP|643}}</ref>
*Grade I: moderate cellularity +/- binucleated cells.
*Grade I: moderate cellularity +/- binucleated cells.
*Grade III: nuclear pleomorphism, mitoses common.
*Grade III: nuclear pleomorphism, mitoses common.
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==Synovial sarcoma==
==Synovial sarcoma==
===General===
===General===
*Does not arise from cartilage.<ref>WMSP P.627.</ref>
*Does not arise from cartilage.<ref name=Ref_WMSP627>{{Ref WMSP|627}}</ref>
*Young adults or adolescents.
*Young adults or adolescents.


===Microscopic===
===Microscopic===
Comes in three flavours:<ref>WMSP P.627.</ref><ref>{{cite journal |author=Schaal CH, Navarro FC, Moraes Neto FA |title=Primary renal sarcoma with morphologic and immunohistochemical aspects compatible with synovial sarcoma |journal=Int Braz J Urol |volume=30 |issue=3 |pages=210–3 |year=2004 |pmid=15689250 |doi= |url=http://www.brazjurol.com.br/may_june_2004/Schaal_ing_210_213.htm}}</ref>
Comes in three flavours:<ref name=Ref_WMSP627>{{Ref WMSP|627}}</ref><ref>{{cite journal |author=Schaal CH, Navarro FC, Moraes Neto FA |title=Primary renal sarcoma with morphologic and immunohistochemical aspects compatible with synovial sarcoma |journal=Int Braz J Urol |volume=30 |issue=3 |pages=210–3 |year=2004 |pmid=15689250 |doi= |url=http://www.brazjurol.com.br/may_june_2004/Schaal_ing_210_213.htm}}</ref>
#Spindle cell sarcoma with features of hemangiopericytoma, i.e. staghorn vessels.
#Spindle cell sarcoma with features of hemangiopericytoma, i.e. staghorn vessels.
#Biphasic synovial sarcoma:
#Biphasic synovial sarcoma:
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===IHC===
===IHC===
Features:<ref>WMSP P.627.</ref>
Features:<ref name=Ref_WMSP627>{{Ref WMSP|627}}</ref>
*Vimentin +ve + cytokeratin and/or EMA +ve.
*Vimentin +ve + cytokeratin and/or EMA +ve.
*CD99 +ve.
*CD99 +ve.
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