Melanocytic nevus pathophysiology: Difference between revisions

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*While giant congenital melanocytic nevi (CMN) have somatic gain-of-function mutations in NRAS.<ref name="pmid18633438">{{cite journal |vauthors=Dessars B, De Raeve LE, Morandini R, Lefort A, El Housni H, Ghanem GE, Van den Eynde BJ, Ma W, Roseeuw D, Vassart G, Libert F, Heimann P |title=Genotypic and gene expression studies in congenital melanocytic nevi: insight into initial steps of melanotumorigenesis |journal=J. Invest. Dermatol. |volume=129 |issue=1 |pages=139–47 |date=January 2009 |pmid=18633438 |doi=10.1038/jid.2008.203 |url=}}</ref><ref name="pmid24129063">{{cite journal |vauthors=Charbel C, Fontaine RH, Malouf GG, Picard A, Kadlub N, El-Murr N, How-Kit A, Su X, Coulomb-L'Hermine A, Tost J, Mourah S, Aractingi S, Guégan S |title=NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic nevi |journal=J. Invest. Dermatol. |volume=134 |issue=4 |pages=1067–1074 |date=April 2014 |pmid=24129063 |doi=10.1038/jid.2013.429 |url=}}</ref>
*While giant congenital melanocytic nevi (CMN) have somatic gain-of-function mutations in NRAS.<ref name="pmid18633438">{{cite journal |vauthors=Dessars B, De Raeve LE, Morandini R, Lefort A, El Housni H, Ghanem GE, Van den Eynde BJ, Ma W, Roseeuw D, Vassart G, Libert F, Heimann P |title=Genotypic and gene expression studies in congenital melanocytic nevi: insight into initial steps of melanotumorigenesis |journal=J. Invest. Dermatol. |volume=129 |issue=1 |pages=139–47 |date=January 2009 |pmid=18633438 |doi=10.1038/jid.2008.203 |url=}}</ref><ref name="pmid24129063">{{cite journal |vauthors=Charbel C, Fontaine RH, Malouf GG, Picard A, Kadlub N, El-Murr N, How-Kit A, Su X, Coulomb-L'Hermine A, Tost J, Mourah S, Aractingi S, Guégan S |title=NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic nevi |journal=J. Invest. Dermatol. |volume=134 |issue=4 |pages=1067–1074 |date=April 2014 |pmid=24129063 |doi=10.1038/jid.2013.429 |url=}}</ref>
*Compared to acquired melanocytic nevi, CMN penetrate into deeper layers of dermis.<ref name="pmid4756859">{{cite journal |vauthors=Mark GJ, Mihm MC, Liteplo MG, Reed RJ, Clark WH |title=Congenital melanocytic nevi of the small and garment type. Clinical, histologic, and ultrastructural studies |journal=Hum. Pathol. |volume=4 |issue=3 |pages=395–418 |date=September 1973 |pmid=4756859 |doi= |url=}}</ref>
*Compared to acquired melanocytic nevi, CMN penetrate into deeper layers of dermis.<ref name="pmid4756859">{{cite journal |vauthors=Mark GJ, Mihm MC, Liteplo MG, Reed RJ, Clark WH |title=Congenital melanocytic nevi of the small and garment type. Clinical, histologic, and ultrastructural studies |journal=Hum. Pathol. |volume=4 |issue=3 |pages=395–418 |date=September 1973 |pmid=4756859 |doi= |url=}}</ref>
*Melanocytes in CMN follow pathyway of nerves and vessels and grow along adenxal structures (eg, hair follicles, sebaceous glands, eccrine ducts) and settle between collagen bundles in a single arrangement.<ref name="pmid6715623">{{cite journal |vauthors= |title=Precursors to malignant melanoma. National Institutes of Health Consensus Development Conference Statement, Oct. 24-26, 1983 |journal=J. Am. Acad. Dermatol. |volume=10 |issue=4 |pages=683–8 |date=April 1984 |pmid=6715623 |doi= |url=}}</ref><ref name="pmid22771898">{{cite journal |vauthors=Kokta V, Hung T, Al Dhaybi R, Lugassy C, Barnhill RL |title=High prevalence of angiotropism in congenital melanocytic nevi: an analysis of 53 cases |journal=Am J Dermatopathol |volume=35 |issue=2 |pages=180–3 |date=April 2013 |pmid=22771898 |doi=10.1097/DAD.0b013e318260908c |url=}}</ref>


===Gross Pathology===
===Gross Pathology===

Revision as of 16:24, 15 May 2019

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Melanocytic nevus Microchapters

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Overview

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Differentiating Melanocytic Nevus from other Diseases

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Editors-In-Chief: Martin I. Newman, M.D., FACS, Cleveland Clinic Florida, [1];Associate Editor(s)-in-Chief: Qurrat-ul-ain Abid, M.D.[2] Michel C. Samson, M.D., FRCSC, FACS [3]

Overview

Melanocytic nevus is a benign growth on the skin (usually tan, brown, or flesh-colored) that contains a cluster of melanocytes and surrounding supportive tissue.

Pathophysiology

Congenital melanocytic nevi (CMN)

  • Congenital melanocytic nevi (CMN) are hamartomas lesions.
  • During embryogenesis clonal proliferations of benign melanocytes may give rise to melanocytic nevi.[1][2]
  • BRAF V600E mutations have a very high corelation with small congenital melanocytic nevi (CMN), acquired melanocytic nevi and cutaneous melanomas.[3][4]
  • While giant congenital melanocytic nevi (CMN) have somatic gain-of-function mutations in NRAS.[5][6]
  • Compared to acquired melanocytic nevi, CMN penetrate into deeper layers of dermis.[7]
  • Melanocytes in CMN follow pathyway of nerves and vessels and grow along adenxal structures (eg, hair follicles, sebaceous glands, eccrine ducts) and settle between collagen bundles in a single arrangement.[8][9]

Gross Pathology

Melanocytic naevus


References

  1. Tannous ZS, Mihm MC, Sober AJ, Duncan LM (February 2005). "Congenital melanocytic nevi: clinical and histopathologic features, risk of melanoma, and clinical management". J. Am. Acad. Dermatol. 52 (2): 197–203. doi:10.1016/j.jaad.2004.07.020. PMID 15692463.
  2. Price HN, Schaffer JV (2010). "Congenital melanocytic nevi-when to worry and how to treat: Facts and controversies". Clin. Dermatol. 28 (3): 293–302. doi:10.1016/j.clindermatol.2010.04.004. PMID 20541682.
  3. Ichii-Nakato N, Takata M, Takayanagi S, Takashima S, Lin J, Murata H, Fujimoto A, Hatta N, Saida T (September 2006). "High frequency of BRAFV600E mutation in acquired nevi and small congenital nevi, but low frequency of mutation in medium-sized congenital nevi". J. Invest. Dermatol. 126 (9): 2111–8. doi:10.1038/sj.jid.5700366. PMID 16691193.
  4. Wu J, Rosenbaum E, Begum S, Westra WH (December 2007). "Distribution of BRAF T1799A(V600E) mutations across various types of benign nevi: implications for melanocytic tumorigenesis". Am J Dermatopathol. 29 (6): 534–7. doi:10.1097/DAD.0b013e3181584950. PMID 18032947.
  5. Dessars B, De Raeve LE, Morandini R, Lefort A, El Housni H, Ghanem GE, Van den Eynde BJ, Ma W, Roseeuw D, Vassart G, Libert F, Heimann P (January 2009). "Genotypic and gene expression studies in congenital melanocytic nevi: insight into initial steps of melanotumorigenesis". J. Invest. Dermatol. 129 (1): 139–47. doi:10.1038/jid.2008.203. PMID 18633438.
  6. Charbel C, Fontaine RH, Malouf GG, Picard A, Kadlub N, El-Murr N, How-Kit A, Su X, Coulomb-L'Hermine A, Tost J, Mourah S, Aractingi S, Guégan S (April 2014). "NRAS mutation is the sole recurrent somatic mutation in large congenital melanocytic nevi". J. Invest. Dermatol. 134 (4): 1067–1074. doi:10.1038/jid.2013.429. PMID 24129063.
  7. Mark GJ, Mihm MC, Liteplo MG, Reed RJ, Clark WH (September 1973). "Congenital melanocytic nevi of the small and garment type. Clinical, histologic, and ultrastructural studies". Hum. Pathol. 4 (3): 395–418. PMID 4756859.
  8. "Precursors to malignant melanoma. National Institutes of Health Consensus Development Conference Statement, Oct. 24-26, 1983". J. Am. Acad. Dermatol. 10 (4): 683–8. April 1984. PMID 6715623.
  9. Kokta V, Hung T, Al Dhaybi R, Lugassy C, Barnhill RL (April 2013). "High prevalence of angiotropism in congenital melanocytic nevi: an analysis of 53 cases". Am J Dermatopathol. 35 (2): 180–3. doi:10.1097/DAD.0b013e318260908c. PMID 22771898.


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