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Mucinous nevus

From Wikipedia, the free encyclopedia
Medical condition
Mucinous nevus
Other namesNevus mucinosus
SpecialtyDermatology

Mucinous nevus is a rare cutaneous condition characterized byhamartoma that can be congenital or acquired.[1] Mucinous nevus presents as multiple skin-coloured or brown asymptomaticpapules or plaques. Mucinous nevus is diagnosed based of histological features. Treatment is not needed.

Signs and symptoms

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Mucinous nevus appears as several skin-coloured to brownishpapules or plaques that are asymptomatic; the individual lesions merge and expand to form a unilateral or zosteriform feature that is verrucous or nevoid.[2][3] It normally starts to develop in early adulthood or from birth.[4] The main location is the trunk, which includes the back.[2][5]

Causes

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There has been reports of familial mucinous nevus, however there have been no reports of genetic abnormalities.[5][4]

Diagnosis

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Histologically, diffuse band-likemucin deposits in the uppermost layer of thedermis are indicative of mucinous nevus.[6]Hyaluronic acid is assumed to be the component ofmucin since it reacts positively withalcian blue at pH 2.5 but does not at pH 0.5.[7][8]

Treatment

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Mucinous nevi arebenign and don't need to be treated other than for aesthetic reasons.[2]Carbon dioxide laser therapy, scalpeldermabrasion, and surgical excision are treatment options.[9]

See also

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References

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  1. ^Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007).Dermatology: 2-Volume Set. St. Louis: Mosby.ISBN 978-1-4160-2999-1.
  2. ^abcCobos, Gabriela; Braunstein, Inbal; Abuabara, Katrina; Chu, Emily Y.; James, William (2014-09-01). "Mucinous Nevus: Report of a Case and Review of the Literature".JAMA Dermatology.150 (9): 1018.doi:10.1001/jamadermatol.2013.9451.ISSN 2168-6068.PMID 25029469.
  3. ^Tardío, Juan C.; Granados, Rosario (2010-07-08). "The cellular component of the mucinous nevus consists of CD34-positive fibroblasts".Journal of Cutaneous Pathology.37 (9). Wiley:1019–1020.doi:10.1111/j.1600-0560.2009.01426.x.ISSN 0303-6987.PMID 19765172.
  4. ^abCHEN, CHIA-WEI; TSAI, TSEN-FANG; CHEN, YU-FU; HUNG, CHIH-MING (2008). "Familial Mucinous Nevus".Pediatric Dermatology.25 (2). Wiley:288–289.doi:10.1111/j.1525-1470.2008.00664.x.ISSN 0736-8046.PMID 18429813.
  5. ^abPerez-Crespo, M; Lopez-Navarro, N; Betlloch, I; Herrera, E; Niveiro, M; Gallego, E (2011-09-25). "Acquired and familial mucinous nevus".International Journal of Dermatology.50 (10). Wiley:1283–1285.doi:10.1111/j.1365-4632.2010.04520.x.ISSN 0011-9059.PMID 21950298.
  6. ^Lee, Min Young; Byun, Ji Yeon; Choi, Hae Young; Choi, You Won (2018)."Mucinous Nevus".Annals of Dermatology.30 (4). Korean Dermatological Association and The Korean Society for Investigative Dermatology:465–467.doi:10.5021/ad.2018.30.4.465.ISSN 1013-9087.PMC 6029955.PMID 30065589.
  7. ^Lim, J-H.; Cho, S-H.; Kim, H-O.; Kim, C-W.; Park, Y-M. (2003). "Mucinous naevus with atypical features".British Journal of Dermatology.148 (5). Oxford University Press (OUP):1064–1066.doi:10.1046/j.1365-2133.2003.05334.x.ISSN 0007-0963.PMID 12786849.
  8. ^BRAKMAN, M.; STARINK, TH.M.; TAFELKRUYER, J.; BOS, J.D. (1994). "Linear connective tissue naevus of the proteoglycan type ('naevus mucinosus')".British Journal of Dermatology.131 (3). Oxford University Press (OUP):368–370.doi:10.1111/j.1365-2133.1994.tb08526.x.ISSN 0007-0963.
  9. ^Chi, Ching-Chi; Wang, Shu-Hui; Lin, Paul Y. (2009). "Combined epidermal-connective tissue nevus of proteoglycan (a type of mucinous nevus): a case report and literature review".Journal of Cutaneous Pathology.36 (7). Wiley:808–811.doi:10.1111/j.1600-0560.2008.01123.x.ISSN 0303-6987.PMID 19519615.

Further reading

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External links

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Classification
External resources
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