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{{ Infobox diagnosis | |||
| Name = {{PAGENAME}} | |||
| Image = Cutaneous_leiomyosarcoma_-_high_mag.jpg | |||
| Width = | |||
| Caption = Leiomyosarcoma. [[H&E stain]]. | |||
| Micro = fasciclar arrangement (characteristic of smooth muscle), features of malignancy (usually need 2 of 3): † (1) nuclear atypia, (2) tumour cell necrosis, (3) mitoses - variable & definitions suffer from [[HPFitis]] | |||
| Subtypes = major: spindled leiomyosarcoma (leiomyosarcoma NOS), epithelioid leiomyosarcoma, myxoid leiomyosarcoma; minor: leiomyosarcoma with prominent intravascular growth, leiomyosarcoma with osteoclast-type cells, leiomyosarcoma with clear cells, leiomyosarcoma with xanthoma-type cells | |||
| LMDDx = [[pleomorphic undifferentiated sarcoma]], [[atypical fibroxanthoma]] (skin only), [[EBV-associated smooth muscle tumour]], [[carcinosarcoma]], [[smooth muscle tumour of uncertain malignant potential]] (STUMP), [[endometrial stromal sarcoma]], [[atypical leiomyoma]] (symplastic leiomyoma) | |||
| Stains = | |||
| IHC = | |||
| EM = | |||
| Molecular = | |||
| IF = | |||
| Gross = "fleshy" appearance, necrosis, large size | |||
| Grossing = | |||
| Site = [[uterus]], [[skin]], others | |||
| Assdx = | |||
| Syndromes = [[hereditary leiomyomatosis and renal cell cancer]] | |||
| Clinicalhx = | |||
| Signs = | |||
| Symptoms = | |||
| Prevalence = uncommon | |||
| Bloodwork = | |||
| Rads = | |||
| Endoscopy = | |||
| Prognosis = poor | |||
| Other = | |||
| ClinDDx = | |||
}} | |||
'''Leiomyosarcoma''' is a malignant tumour of smooth muscle. It is seen in various places including the [[uterus]] and [[skin]]. | '''Leiomyosarcoma''' is a malignant tumour of smooth muscle. It is seen in various places including the [[uterus]] and [[skin]]. | ||
==General== | ==General== | ||
*Poor prognosis. | *Poor prognosis - usually. | ||
**In locally advanced/metastatic disease (arising from the uterus) the median survival is 12-14 months.<ref>{{Cite journal | last1 = Hadoux | first1 = J. | last2 = Morice | first2 = P. | last3 = Lhommé | first3 = C. | last4 = Duvillard | first4 = P. | last5 = Balleyguier | first5 = C. | last6 = Haie-Meder | first6 = C. | last7 = Gouy | first7 = S. | last8 = Uzan | first8 = C. | last9 = Mazeron | first9 = R. | title = [Uterine leiomyosarcoma: epidemiology, pathology, biology, diagnosis, prognosis and treatment]. | journal = Bull Cancer | volume = 100 | issue = 9 | pages = 903-15 | month = Sep | year = 2013 | doi = 10.1684/bdc.2013.1801 | PMID = 24004576 }}</ref> | |||
*Do not (generally) arise from leiomyomas. | *Do not (generally) arise from leiomyomas. | ||
*Often singular, i.e. one tumour; unlike | *Often singular, i.e. one tumour; unlike [[leiomyoma]]s (which are often multiple). | ||
*May be a part of [[hereditary leiomyomatosis and renal cell cancer]]. | |||
Note: | |||
*''Skin leiomyosarcoma'' do so well it has been proposed to no longer refer to them as ''sarcomas''.<ref name=pmid21358302/> | |||
==Gross== | ==Gross== | ||
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==Microscopic== | ==Microscopic== | ||
Features: | Features: | ||
* | *Usually a cellular lesion. | ||
* | *Fasciclar arrangement: | ||
**Whorled look at low power. | **Whorled look at low power. | ||
**Groups of spindle cells cut peripendicular to their long axis adjacent to groups of spindle cells cut in the plane of their long axis. | **Groups of spindle cells cut peripendicular to their long axis adjacent to groups of spindle cells cut in the plane of their long axis. | ||
*Features of malignancy (need | *Features of malignancy (usually need 2 of 3): † | ||
*# | *#Nuclear atypia. | ||
*# | *#Tumour cell necrosis. | ||
*#*Should be patchy/multifocal. | *#*Should be patchy/multifocal. | ||
*#**Zonal necrosis is suggestive of vascular cause. | *#**Zonal necrosis is suggestive of vascular cause. | ||
*#Mitoses - '''key feature''' | *#Mitoses - '''key feature''' - definitions suffer from [[HPFitis]]: | ||
*#*10 mitoses/HPF. | *#*>=10 mitoses/10 HPF - if spindled.<ref name=Ref_GP281>{{Ref GP|281}}</ref> | ||
*#*5 mitoses/HPF - if epithelioid. | *#*>=5 mitoses/10 HPF - if epithelioid.<ref name=Ref_GP281>{{Ref GP|281}}</ref> | ||
*#*2 mitoses/HPF - if myxoid. | *#*>=2 mitoses/10 HPF - if [[myxoid]].<ref name=Ref_GP281>{{Ref GP|281}}</ref> | ||
*#*>=1 mitosis/HPF - if cutaneous.<ref name=pmid21358302>{{cite journal |author=Kraft S, Fletcher CD |title=Atypical intradermal smooth muscle neoplasms: clinicopathologic analysis of 84 cases and a reappraisal of cutaneous "leiomyosarcoma" |journal=Am. J. Surg. Pathol. |volume=35 |issue=4 |pages=599–607 |year=2011 |month=April |pmid=21358302 |doi=10.1097/PAS.0b013e31820e6093 |url=}}</ref> | *#*>=1 mitosis/10 HPF - if cutaneous.<ref name=pmid21358302>{{cite journal |author=Kraft S, Fletcher CD |title=Atypical intradermal smooth muscle neoplasms: clinicopathologic analysis of 84 cases and a reappraisal of cutaneous "leiomyosarcoma" |journal=Am. J. Surg. Pathol. |volume=35 |issue=4 |pages=599–607 |year=2011 |month=April |pmid=21358302 |doi=10.1097/PAS.0b013e31820e6093 |url=}}</ref> | ||
*+/-Heterologous elements, e.g. malignant cartilage or bone.<ref name=pmid22833086>{{Cite journal | last1 = Anh Tran | first1 = T. | last2 = Holloway | first2 = RW. | title = Metastatic leiomyosarcoma of the uterus with heterologous differentiation to malignant mesenchymoma. | journal = Int J Gynecol Pathol | volume = 31 | issue = 5 | pages = 453-7 | month = Sep | year = 2012 | doi = 10.1097/PGP.0b013e318246977d | PMID = 22833086 }}</ref> | |||
Notes: | |||
*† In deep soft tissue. 1 of 3 criteria is considered enough.<ref>URL: [http://surgpathcriteria.stanford.edu/softsmoothmuscle/soft_tissue_leiomyosarcoma/differentialdiagnosis.html http://surgpathcriteria.stanford.edu/softsmoothmuscle/soft_tissue_leiomyosarcoma/differentialdiagnosis.html]. Accessed on: 10 May 2013.</ref> | |||
*Leiomyosarcoma ''de facto'' trumps other sarcomas.<ref name=pmid22833086/> | |||
*Mitotic rate seems to be a relatively weak predictor; modest rate may be malignant and a high rate benign.<ref name=pmid9388868>{{Cite journal | last1 = Guo | first1 = L. | last2 = Liu | first2 = T. | last3 = Huang | first3 = H. | title = [Reappraisal of the pathological criteria for uterine leiomyosarcoma]. | journal = Zhonghua Bing Li Xue Za Zhi | volume = 25 | issue = 5 | pages = 266-9 | month = Oct | year = 1996 | doi = | PMID = 9388868 }}</ref> | |||
DDx: | |||
*[[Pleomorphic undifferentiated sarcoma]]. | |||
*[[EBV-associated smooth muscle tumour]] - rare, immunoincompetent individuals. | |||
*[[Carcinosarcoma]]. | |||
*[[Smooth muscle tumour of uncertain malignant potential]] (STUMP). | |||
*[[Endometrial stromal sarcoma]]. | |||
*[[Atypical leiomyoma]]. | |||
===Images=== | |||
Uterine: | |||
<gallery> | |||
Image:Uterine_leiomyosarcoma_%281%29.jpg | Uterine leiomyosarcoma 1 (WC) | |||
Image:Uterine_leiomyosarcoma_%282%29.jpg | Uterine leiomyosarcoma 2 (WC) | |||
</gallery> | |||
Cutaneous: | |||
<gallery> | |||
Image:Cutaneous_leiomyosarcoma_-_intermed_mag.jpg | Cutaneous leiomyosarcoma - intermed. mag. - shows fascicular pattern (WC) | |||
Image:Cutaneous_leiomyosarcoma_-_a_-_intermed_mag.jpg | Cutaneous leiomyosarcoma - intermed. mag. (WC) | |||
Image:Cutaneous_leiomyosarcoma_-_high_mag.jpg | Cutaneous leiomyosarcoma - high mag. (WC) | |||
Image:Cutaneous_leiomyosarcoma_-_very_high_mag.jpg | Cutaneous leiomyosarcoma - very high mag. (WC) | |||
</gallery> | |||
www: | |||
*[http://path.upmc.edu/cases/case107/micro.html Cutaneous leiomyosarcoma (upmc.edu)]. | |||
===Subtypes=== | |||
Major variants:<ref name=Ref_GP284>{{Ref GP|284}}</ref> | |||
*Spindled leiomyosarcoma (leiomyosarcoma NOS) - see above. | |||
*Epithelioid leiomyosarcoma. | |||
*Myxoid leiomyosarcoma. | |||
Minor variants:<ref name=Ref_GP284>{{Ref GP|284}}</ref> | |||
*Leiomyosarcoma with prominent intravascular growth. | |||
*Leiomyosarcoma with osteoclast-type cells. | |||
*Leiomyosarcoma with clear cells. | |||
*Leiomyosarcoma with xanthoma-type cells. | |||
====Epithelioid leiomyosarcoma==== | |||
Features:<ref name=Ref_GP281>{{Ref GP|281}}</ref> | |||
*>50% epithelial appearance. | |||
*>=5 mitoses/HPF - definition suffers from [[HPFitis]]. | |||
Image: | |||
*[http://www.webpathology.com/image.asp?n=12&Case=61 Epithelioid leiomyosarcoma (webpathology.com)]. | |||
====Myxoid leiomyosarcoma==== | |||
Features:<ref name=Ref_GP281>{{Ref GP|281}}</ref> | |||
*>=2 mitoses/HPF - definition suffers from [[HPFitis]]. | |||
*May have minimal nuclear atypia. | |||
==IHC== | |||
Features: | |||
*Positive for SMC markers. | *Positive for SMC markers. | ||
**Desmin - present in all three types of muscle. | **Desmin - present in all three types of muscle. | ||
** | **H-caldesmon. | ||
**Smooth muscle myosin. | **Smooth muscle myosin. | ||
*CD10 -ve. | |||
**May be +ve.<ref name=Ref_GP284>{{Ref GP|284}}</ref> | |||
**Some use in the context of uterine lesions -- CD10 +ve in [[endometrial stromal sarcoma]]. | |||
Others:<ref name=Ref_GP284>{{Ref GP|284}}</ref> | |||
*ER, PR, AR +ve -- 30-40% of the time. | |||
*CD117 +ve/-ve. | |||
*p53 +ve. | |||
*MIB1 high. | |||
*Kertins usu. -ve -- more often +ve in epithelioid variant. | |||
==Sign out== | |||
<pre> | |||
SKIN LESION, LEFT SHOULDER (SUTURE AT 12 O'CLOCK), WIDE EXCISION: | |||
- LEIOMYOSARCOMA, MARGINALLY EXCISED. | |||
-- PLEASE SEE TUMOUR SUMMARY. | |||
- DERMAL SCAR. | |||
</pre> | |||
==See also== | ==See also== | ||
*[[Soft tissue lesions]]. | *[[Soft tissue lesions]]. | ||
*[[Uterine tumours]]. | *[[Uterine tumours]]. | ||
*[[Leiomyoma]]. | |||
==References== | ==References== | ||
{{Reflist| | {{Reflist|2}} | ||
[[Category:Soft tissue]] | [[Category:Soft tissue lesions]] | ||
[[Category:Gynecologic pathology]] | [[Category:Gynecologic pathology]] |
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