Dermatofibroma natural history, complications and prognosis: Difference between revisions
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==Overview== | ==Overview== | ||
Dermatofibroma usually [[Development|develops]] in the third decade of life, and most of them are [[asymptomatic]]. | Dermatofibroma usually [[Development|develops]] in the third decade of life, and most of them are [[asymptomatic]]. Common [[complications]] of dermatofibroma are related to [[Excision|excisional]] removing of the [[lesion]] and include, [[bleeding]], [[infection]] and [[scar]]. [[Prognosis]] is generally excellent. Although, in very [[rare]] cases [[metastases]] are seen. | ||
Common [[complications]] of dermatofibroma are related to [[Excision|excisional]] removing of the [[lesion]] and include, [[bleeding]], [[infection]] and [[scar]]. | |||
[[Prognosis]] is generally excellent. Although, in very [[rare]] cases [[metastases]] are seen. | |||
==Natural History, Complications, and Prognosis== | ==Natural History, Complications, and Prognosis== | ||
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| title = Dermatofibroma | | title = Dermatofibroma | ||
| year = 2019 | | year = 2019 | ||
| month = | | month = | ||
| pmid = 29262213 | | pmid = 29262213 | ||
}}</ref> | |url=|first=|date=|journal=|volume=|pages=|via=}}</ref> | ||
**[[Bleeding]] | **[[Bleeding]] | ||
**[[Infection]] | **[[Infection]] | ||
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===Prognosis=== | ===Prognosis=== | ||
*[[Prognosis]] is generally excellent. Although, in very [[rare]] cases [[metastases]] are seen. | *[[Prognosis]] is generally excellent. Although, in very [[rare]] cases [[metastases]] are seen.<ref name="RomanoFritchie2017">{{cite journal|last1=Romano|first1=Ryan C.|last2=Fritchie|first2=Karen J.|title=Fibrohistiocytic Tumors|journal=Clinics in Laboratory Medicine|volume=37|issue=3|year=2017|pages=603–631|issn=02722712|doi=10.1016/j.cll.2017.05.007}}</ref> | ||
==References== | ==References== | ||
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[[Category:Oncology]] | [[Category:Oncology]] | ||
[[Category:Up-To-Date]] | [[Category:Up-To-Date]] | ||
[[Category:Dermatology]] | [[Category:Dermatology]] | ||
Latest revision as of 21:18, 29 July 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Homa Najafi, M.D.[2]
Overview
Dermatofibroma usually develops in the third decade of life, and most of them are asymptomatic. Common complications of dermatofibroma are related to excisional removing of the lesion and include, bleeding, infection and scar. Prognosis is generally excellent. Although, in very rare cases metastases are seen.
Natural History, Complications, and Prognosis
Natural History
- Dermatofibroma usually develops in the third decade of life, and most of them are asymptomatic.[1][2][3]
Complications
- Common complications of dermatofibroma are related to excisional removing of the lesion and include:[4]
Prognosis
- Prognosis is generally excellent. Although, in very rare cases metastases are seen.[5]
References
- ↑ Agarwal, Atin; Gopinath, Arun; Tetzlaff, Michael T.; Prieto, Victor G. (2017). "Phosphohistone-H3 and Ki67". The American Journal of Dermatopathology. 39 (7): 504–507. doi:10.1097/DAD.0000000000000690. ISSN 0193-1091.
- ↑ Buehler, Darya; Weisman, Paul (2017). "Soft Tissue Tumors of Uncertain Histogenesis". Clinics in Laboratory Medicine. 37 (3): 647–671. doi:10.1016/j.cll.2017.06.005. ISSN 0272-2712.
- ↑ Han, Tae Young; Chang, Hee Sun; Lee, June Hyun Kyung; Lee, Won-Mi; Son, Sook-Ja (2011). "A Clinical and Histopathological Study of 122 Cases of Dermatofibroma (Benign Fibrous Histiocytoma)". Annals of Dermatology. 23 (2): 185. doi:10.5021/ad.2011.23.2.185. ISSN 1013-9087.
- ↑ David J.. Myers & Eric P.. Fillman (2019). "Dermatofibroma". PMID 29262213.
- ↑ Romano, Ryan C.; Fritchie, Karen J. (2017). "Fibrohistiocytic Tumors". Clinics in Laboratory Medicine. 37 (3): 603–631. doi:10.1016/j.cll.2017.05.007. ISSN 0272-2712.