Dermatofibrosarcoma protuberans - Revision history

Michael: tweak

2014-06-21T11:35:25Z

tweak

← Older revision		Revision as of 11:35, 21 June 2014
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	\| Signs =		\| Signs =
	\| Symptoms =		\| Symptoms =
	\| Prevalence =		\| Prevalence = uncommon
	\| Bloodwork =		\| Bloodwork =
	\| Rads =		\| Rads =
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	\| Other =		\| Other =
	\| ClinDDx =		\| ClinDDx =
			\| Tx = wide excision
	}}		}}
	'''Dermatofibrosarcoma protuberans''', abbreviated '''DFSP''', is a rare locally aggressive [[dermatologic neoplasms\|tumour of the skin]].		'''Dermatofibrosarcoma protuberans''', abbreviated '''DFSP''', is a rare locally aggressive [[dermatologic neoplasms\|tumour of the skin]].

Michael: /* General */

2013-11-11T21:39:43Z

General

← Older revision		Revision as of 21:39, 11 November 2013
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	==General==		==General==
	*Destroys adnexal structures.		*Destroys adnexal structures - somewhat unusual for a mostly benign tumour.
	*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>		*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>
	*Typically slow growing.<ref name=pmid23327727>{{Cite journal \| last1 = Llombart \| first1 = B. \| last2 = Serra-Guillén \| first2 = C. \| last3 = Monteagudo \| first3 = C. \| last4 = López Guerrero \| first4 = JA. \| last5 = Sanmartín \| first5 = O. \| title = Dermatofibrosarcoma protuberans: a comprehensive review and update on diagnosis and management. \| journal = Semin Diagn Pathol \| volume = 30 \| issue = 1 \| pages = 13-28 \| month = Feb \| year = 2013 \| doi = 10.1053/j.semdp.2012.01.002 \| PMID = 23327727 }}</ref>		*Typically slow growing.<ref name=pmid23327727>{{Cite journal \| last1 = Llombart \| first1 = B. \| last2 = Serra-Guillén \| first2 = C. \| last3 = Monteagudo \| first3 = C. \| last4 = López Guerrero \| first4 = JA. \| last5 = Sanmartín \| first5 = O. \| title = Dermatofibrosarcoma protuberans: a comprehensive review and update on diagnosis and management. \| journal = Semin Diagn Pathol \| volume = 30 \| issue = 1 \| pages = 13-28 \| month = Feb \| year = 2013 \| doi = 10.1053/j.semdp.2012.01.002 \| PMID = 23327727 }}</ref>

Michael: /* General */

2013-11-11T21:39:12Z

General

← Older revision		Revision as of 21:39, 11 November 2013
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	==General==		==General==
	*Dermal location.
	*Destroys adnexal structures.		*Destroys adnexal structures.
	*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>		*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>

Michael: /* General */

2013-11-11T21:39:00Z

General

← Older revision		Revision as of 21:39, 11 November 2013
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	*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>		*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>
	*Typically slow growing.<ref name=pmid23327727>{{Cite journal \| last1 = Llombart \| first1 = B. \| last2 = Serra-Guillén \| first2 = C. \| last3 = Monteagudo \| first3 = C. \| last4 = López Guerrero \| first4 = JA. \| last5 = Sanmartín \| first5 = O. \| title = Dermatofibrosarcoma protuberans: a comprehensive review and update on diagnosis and management. \| journal = Semin Diagn Pathol \| volume = 30 \| issue = 1 \| pages = 13-28 \| month = Feb \| year = 2013 \| doi = 10.1053/j.semdp.2012.01.002 \| PMID = 23327727 }}</ref>		*Typically slow growing.<ref name=pmid23327727>{{Cite journal \| last1 = Llombart \| first1 = B. \| last2 = Serra-Guillén \| first2 = C. \| last3 = Monteagudo \| first3 = C. \| last4 = López Guerrero \| first4 = JA. \| last5 = Sanmartín \| first5 = O. \| title = Dermatofibrosarcoma protuberans: a comprehensive review and update on diagnosis and management. \| journal = Semin Diagn Pathol \| volume = 30 \| issue = 1 \| pages = 13-28 \| month = Feb \| year = 2013 \| doi = 10.1053/j.semdp.2012.01.002 \| PMID = 23327727 }}</ref>
	*Usually second to fifth decade..<ref name=pmid23327727/>		*Usually second to fifth decade.<ref name=pmid23327727/>

	Treatment:<ref name=Ref_PBoD8_1183>{{Ref PBoD8\|1183}}</ref>		Treatment:<ref name=Ref_PBoD8_1183>{{Ref PBoD8\|1183}}</ref>

Michael: more

2013-11-11T21:35:22Z

← Older revision		Revision as of 21:35, 11 November 2013
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	\| Gross = firm plaque +/-ulceration		\| Gross = firm plaque +/-ulceration
	\| Grossing =		\| Grossing =
	\| Site = [[skin]] - usually trunk		\| Site = [[skin]] - usually trunk or proximal extremities
	\| Assdx =		\| Assdx =
	\| Syndromes =		\| Syndromes =
	\| Clinicalhx =		\| Clinicalhx = second to fifth decade
	\| Signs =		\| Signs =
	\| Symptoms =		\| Symptoms =
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	\| Rads =		\| Rads =
	\| Endoscopy =		\| Endoscopy =
	\| Prognosis =		\| Prognosis = moderate, locally aggressive, rarely metastases
	\| Other =		\| Other =
	\| ClinDDx =		\| ClinDDx =
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	*Destroys adnexal structures.		*Destroys adnexal structures.
	*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>		*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>
			*Typically slow growing.<ref name=pmid23327727>{{Cite journal \| last1 = Llombart \| first1 = B. \| last2 = Serra-Guillén \| first2 = C. \| last3 = Monteagudo \| first3 = C. \| last4 = López Guerrero \| first4 = JA. \| last5 = Sanmartín \| first5 = O. \| title = Dermatofibrosarcoma protuberans: a comprehensive review and update on diagnosis and management. \| journal = Semin Diagn Pathol \| volume = 30 \| issue = 1 \| pages = 13-28 \| month = Feb \| year = 2013 \| doi = 10.1053/j.semdp.2012.01.002 \| PMID = 23327727 }}</ref>
			*Usually second to fifth decade..<ref name=pmid23327727/>

	Treatment:<ref name=Ref_PBoD8_1183>{{Ref PBoD8\|1183}}</ref>		Treatment:<ref name=Ref_PBoD8_1183>{{Ref PBoD8\|1183}}</ref>
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	*[[Solitary fibrous tumour]].		*[[Solitary fibrous tumour]].
	*[[Undifferentiated pleomorphic sarcoma]].		*[[Undifferentiated pleomorphic sarcoma]].

			===Subtypes===
			Numerous variants/subtypes are described:<ref name=pmid23327727>{{Cite journal \| last1 = Llombart \| first1 = B. \| last2 = Serra-Guillén \| first2 = C. \| last3 = Monteagudo \| first3 = C. \| last4 = López Guerrero \| first4 = JA. \| last5 = Sanmartín \| first5 = O. \| title = Dermatofibrosarcoma protuberans: a comprehensive review and update on diagnosis and management. \| journal = Semin Diagn Pathol \| volume = 30 \| issue = 1 \| pages = 13-28 \| month = Feb \| year = 2013 \| doi = 10.1053/j.semdp.2012.01.002 \| PMID = 23327727 }}</ref>
			*Pigmented DFSP (Bednar tumour).
			*Myxoid DFSP.
			*Myoid DFSP.
			*Granular cell DFSP.
			*Sclerotic DFSP.
			*Atrophic DFSP,
			*Giant cell fibroblastoma.
			*DFSP with fibrosarcomatous areas.

	===Images===		===Images===

Michael: +infobox

2013-11-11T21:27:59Z

+infobox

← Older revision		Revision as of 21:27, 11 November 2013
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	'''~~Dermatofibrosarcoma_protuberans~~''', abbreviated ''DFSP'', is a rare locally aggressive [[dermatologic neoplasms\|tumour of the skin]].		{{ Infobox diagnosis
			\| Name = {{PAGENAME}}
			\| Image = Storiform_pattern_-_very_high_mag.jpg
			\| Width =
			\| Caption = DFSP. [[H&E stain]].
			\| Micro = dermal spindle cell lesion with storiform pattern, typically contains adipose tissue within the tumour -- described as "honeycomb pattern" and "Swiss cheese pattern"
			\| Subtypes =
			\| LMDDx = [[dermatofibroma]], [[dermatomyofibroma]], [[nodular fasciitis]]
			\| Stains =
			\| IHC = CD34 +ve, Factor XIIIa -ve
			\| EM =
			\| Molecular = t(17;22)(q22;q15)
			\| IF =
			\| Gross = firm plaque +/-ulceration
			\| Grossing =
			\| Site = [[skin]] - usually trunk
			\| Assdx =
			\| Syndromes =
			\| Clinicalhx =
			\| Signs =
			\| Symptoms =
			\| Prevalence =
			\| Bloodwork =
			\| Rads =
			\| Endoscopy =
			\| Prognosis =
			\| Other =
			\| ClinDDx =
			}}
			'''Dermatofibrosarcoma protuberans''', abbreviated '''DFSP''', is a rare locally aggressive [[dermatologic neoplasms\|tumour of the skin]].

	==General==		==General==
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	Notes:		Notes:
	*Adnexal structure within tumour are preserved -- this is unusual for a malignant tumour -- '''important'''.		*Adnexal structure within tumour are preserved -- this is unusual for a malignant tumour -- '''important'''.


	DDx:		DDx:
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	*Factor XIIIa -ve.		*Factor XIIIa -ve.
	**Usually positive in dermatofibroma.<ref name=pmid7694515>{{cite journal \|author=Abenoza P, Lillemoe T \|title=CD34 and factor XIIIa in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans \|journal=Am J Dermatopathol \|volume=15 \|issue=5 \|pages=429–34 \|year=1993 \|month=October \|pmid=7694515 \|doi= \|url=}}</ref><ref name=pmid9129699>{{cite journal \|author=Goldblum JR, Tuthill RJ \|title=CD34 and factor-XIIIa immunoreactivity in dermatofibrosarcoma protuberans and dermatofibroma \|journal=Am J Dermatopathol \|volume=19 \|issue=2 \|pages=147–53 \|year=1997 \|month=April \|pmid=9129699 \|doi= \|url=}}</ref>		**Usually positive in dermatofibroma.<ref name=pmid7694515>{{cite journal \|author=Abenoza P, Lillemoe T \|title=CD34 and factor XIIIa in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans \|journal=Am J Dermatopathol \|volume=15 \|issue=5 \|pages=429–34 \|year=1993 \|month=October \|pmid=7694515 \|doi= \|url=}}</ref><ref name=pmid9129699>{{cite journal \|author=Goldblum JR, Tuthill RJ \|title=CD34 and factor-XIIIa immunoreactivity in dermatofibrosarcoma protuberans and dermatofibroma \|journal=Am J Dermatopathol \|volume=19 \|issue=2 \|pages=147–53 \|year=1997 \|month=April \|pmid=9129699 \|doi= \|url=}}</ref>
	*~~S100~~ -ve (screen for melanoma).		*S-100 -ve (screen for melanoma).
	*Caldesmin -ve (screen for muscle differentiation).		*Caldesmin -ve (screen for muscle differentiation).
	*Beta-catenin. (???)		*Beta-catenin. (???)
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	==See also==		==See also==
	*[[Dermatologic neoplasms]].		*[[Dermatologic neoplasms]].
			*[[Dermatofibroma]].

	==References==		==References==

Michael: split-out

2013-11-11T21:21:19Z

split-out

← Older revision		Revision as of 21:21, 11 November 2013
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	~~#redirect~~ [[~~Dermatologic_neoplasms#Dermatofibrosarcoma_protuberans~~]]		'''Dermatofibrosarcoma_protuberans''', abbreviated ''DFSP'', is a rare locally aggressive [[dermatologic neoplasms\|tumour of the skin]].

			==General==
			*Dermal location.
			*Destroys adnexal structures.
			*Occasionally transforms to a (more aggressive) [[adult fibrosarcoma\|fibrosarcoma]].<ref name=pmid21128251>{{Cite journal \| last1 = Stacchiotti \| first1 = S. \| last2 = Pedeutour \| first2 = F. \| last3 = Negri \| first3 = T. \| last4 = Conca \| first4 = E. \| last5 = Marrari \| first5 = A. \| last6 = Palassini \| first6 = E. \| last7 = Collini \| first7 = P. \| last8 = Keslair \| first8 = F. \| last9 = Morosi \| first9 = C. \| title = Dermatofibrosarcoma protuberans-derived fibrosarcoma: clinical history, biological profile and sensitivity to imatinib. \| journal = Int J Cancer \| volume = 129 \| issue = 7 \| pages = 1761-72 \| month = Oct \| year = 2011 \| doi = 10.1002/ijc.25826 \| PMID = 21128251 }}</ref>

			Treatment:<ref name=Ref_PBoD8_1183>{{Ref PBoD8\|1183}}</ref>
			*Wide excision.
			*May include [[imatinib]] (Gleevec).

			==Gross==
			Features:<ref name=Ref_PCPBoD8_600>{{Ref PCPBoD8\|600}}</ref>
			*Firm plaque, often bosselated, usually on the trunk.
			*+/-Ulceration.

			Images:
			*[http://dermatlas.med.jhmi.edu/derm/display.cfm?ImageID=-375107780 Protuberant DFSP (dermatlas.med.jhmi.edu)].
			*[http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=-1421097348 Huge DFSP on back (dermatlas.med.jhmi.edu)].
			*[http://dermatlas.med.jhmi.edu/derm/indexDisplay.cfm?ImageID=-109598044 Protuberant DFSP - gross and histology (dermatlas.med.jhmi.edu)].

			==Microscopic==
			Features:<ref name=Ref_PBoD8_1183>{{Ref PBoD8\|1183}}</ref>
			*Dermal spindle cell lesion with storiform pattern.
			**Spokes of the wheel-pattern.
			*Contains adipose tissue within the tumour -- '''key feature'''.
			**Described as "honeycomb pattern" and "Swiss cheese pattern".

			Notes:
			*Adnexal structure within tumour are preserved -- this is unusual for a malignant tumour -- '''important'''.


			DDx:
			*[[Dermatofibroma]] - main DDx - has entrapment of collagen bundles at the edge of the lesion.
			*[[Dermatomyofibroma]].<ref name=Ref_Derm504>{{Ref Derm\|504}}</ref>
			*[[Nodular fasciitis]].

			DDx of storiform pattern:
			*DFSP.
			*Dermatofibroma.
			*[[Solitary fibrous tumour]].
			*[[Undifferentiated pleomorphic sarcoma]].

			===Images===
			<gallery>
			Image:SkinTumors-P9280838.JPG \| DFSP with fat entrapped. (WC)
			Image:SkinTumors-P9270829.JPG \| DFSP - high mag. (WC)
			Image:Storiform_pattern_-_intermed_mag.jpg \| DFSP - storiform pattern - intermed. mag. (WC/Nephron)
			Image:Storiform_pattern_-_very_high_mag.jpg \| DFSP - storiform pattern - very high mag. (WC/Nephron)
			</gallery>
			www:
			*[http://webpathology.com/image.asp?case=317&n=1 DFSP (webpathology.com)].

			==IHC==
			Panel:<ref>AP. May 2009.</ref>
			*CD34 +ve.
			**Usually negative in dermatofibroma.<ref name=pmid7694515>{{cite journal \|author=Abenoza P, Lillemoe T \|title=CD34 and factor XIIIa in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans \|journal=Am J Dermatopathol \|volume=15 \|issue=5 \|pages=429–34 \|year=1993 \|month=October \|pmid=7694515 \|doi= \|url=}}</ref><ref name=pmid9129699>{{cite journal \|author=Goldblum JR, Tuthill RJ \|title=CD34 and factor-XIIIa immunoreactivity in dermatofibrosarcoma protuberans and dermatofibroma \|journal=Am J Dermatopathol \|volume=19 \|issue=2 \|pages=147–53 \|year=1997 \|month=April \|pmid=9129699 \|doi= \|url=}}</ref>
			*Factor XIIIa -ve.
			**Usually positive in dermatofibroma.<ref name=pmid7694515>{{cite journal \|author=Abenoza P, Lillemoe T \|title=CD34 and factor XIIIa in the differential diagnosis of dermatofibroma and dermatofibrosarcoma protuberans \|journal=Am J Dermatopathol \|volume=15 \|issue=5 \|pages=429–34 \|year=1993 \|month=October \|pmid=7694515 \|doi= \|url=}}</ref><ref name=pmid9129699>{{cite journal \|author=Goldblum JR, Tuthill RJ \|title=CD34 and factor-XIIIa immunoreactivity in dermatofibrosarcoma protuberans and dermatofibroma \|journal=Am J Dermatopathol \|volume=19 \|issue=2 \|pages=147–53 \|year=1997 \|month=April \|pmid=9129699 \|doi= \|url=}}</ref>
			*S100 -ve (screen for melanoma).
			*Caldesmin -ve (screen for muscle differentiation).
			*Beta-catenin. (???)
			*MIB1 (proliferation marker).
			**Should not be confused with ''MIB-1'' a gene that regulates [[apoptosis]].

			==Molecular==
			A characteristic [[translocation]] is seen:<ref>{{Ref PBoD8\|1249}}</ref>
			t(17;22)(q22;q15) COLA1/PDGFB.

			==See also==
			*[[Dermatologic neoplasms]].

			==References==
			{{Reflist\|2}}

	[[Category:Diagnosis]]		[[Category:Diagnosis]]
			[[Category:Dermatologic neoplasms]]

Michael: +cat.

2011-10-18T03:23:52Z

+cat.

← Older revision		Revision as of 03:23, 18 October 2011
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	#redirect [[Dermatologic_neoplasms#Dermatofibrosarcoma_protuberans]]		#redirect [[Dermatologic_neoplasms#Dermatofibrosarcoma_protuberans]]

			[[Category:Diagnosis]]

Michael: fix redirect

2011-03-21T01:10:45Z

fix redirect

← Older revision		Revision as of 01:10, 21 March 2011
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	#redirect [[~~Dermatofibrosarcoma protuberans~~]]		#redirect [[Dermatologic_neoplasms#Dermatofibrosarcoma_protuberans]]

Michael: redirect for now

2011-03-21T01:10:19Z

redirect for now

New page

#redirect [[Dermatofibrosarcoma protuberans]]