High prevalence of angiotropism in congenital melanocytic nevi: an analysis of 53 cases
- PMID: 22771898
- DOI: 10.1097/DAD.0b013e318260908c
High prevalence of angiotropism in congenital melanocytic nevi: an analysis of 53 cases
Abstract
The mechanisms responsible for the development of congenital melanocytic nevi (CMN) have yet to be elucidated. A potential clue to their origin is the observation of angiotropism of nevus cells in CMN. Interestingly, neural crest stem cells (NCSCs), the precursors of melanocytes, demonstrate angiotropism in the embryo. There is accumulating evidence that NCSCs migrate along the external surfaces of vessels during a portion of their journey to the skin. Comparable angiotropism and migration of melanoma cells have been described as extravascular migratory metastasis in melanoma. In this report, we systematically examined for the first time, the frequency of angiotropism in 53 CMN. The lesions originated from 27 females and 26 males with an average age of 9.81 years (range 0.42-28 years). The mean nevus size was 7.43 cm (range 0.3-40 cm). Twenty-seven (50.9%) of the 53 lesions were less than 1.5 cm in diameter. Sixteen nevi (30.2%) were medium sized (1.5-19.9 cm), and 10 CMN (18.9%) were large/giant (>20 cm in diameter). The trunk was the most common location (23/53) followed by the head and neck (17/53). Thirty-eight (71.7%) of the 53 lesions were compound melanocytic nevi, and 15 (28.3%) of the 53 lesions were dermal nevi. In summary, angiotropism was observed in 50 (94.3%) of 53 cases. Consequently, such angiotropism may potentially explain the origin of the precursor cells giving rise to CMN. Further explanations concerning dysregulated growth are clearly needed for the actual appearance of CMN and their physical characteristics.
Similar articles
-
Angiotropic neonatal congenital melanocytic nevus: how extravascular migration of melanocytes may explain the development of congenital nevi.Am J Dermatopathol. 2010 Jul;32(5):495-9. doi: 10.1097/DAD.0b013e3181c6afce. Am J Dermatopathol. 2010. PMID: 20442637
-
Age- and site-specific variation in the dermoscopic patterns of congenital melanocytic nevi: an aid to accurate classification and assessment of melanocytic nevi.Arch Dermatol. 2007 Aug;143(8):1007-14. doi: 10.1001/archderm.143.8.1007. Arch Dermatol. 2007. PMID: 17709659
-
Congenital melanocytic nevi-when to worry and how to treat: Facts and controversies.Clin Dermatol. 2010 May-Jun;28(3):293-302. doi: 10.1016/j.clindermatol.2010.04.004. Clin Dermatol. 2010. PMID: 20541682
-
New recommendations for the categorization of cutaneous features of congenital melanocytic nevi.J Am Acad Dermatol. 2013 Mar;68(3):441-51. doi: 10.1016/j.jaad.2012.05.043. Epub 2012 Sep 13. J Am Acad Dermatol. 2013. PMID: 22982004
-
Congenital melanocytic nevi.Clin Lab Med. 2011 Jun;31(2):267-80. doi: 10.1016/j.cll.2011.03.004. Clin Lab Med. 2011. PMID: 21549240 Review.
Cited by
-
Lymphatic invasion and angiotropism in primary cutaneous melanoma.Lab Invest. 2017 Feb;97(2):118-129. doi: 10.1038/labinvest.2016.131. Epub 2016 Dec 19. Lab Invest. 2017. PMID: 27991909
-
Spitzoid melanoma of childhood: a case series and review.Melanoma Manag. 2015 May;2(2):121-125. doi: 10.2217/mmt.15.6. Epub 2015 May 18. Melanoma Manag. 2015. PMID: 30190841 Free PMC article.
-
Histopathological and Immunohistochemical Features of Small to Big Satellite Nevus Uncover the Nevogenesis of Large/Giant Congenital Melanocytic Nevus.J Immunol Res. 2022 Dec 5;2022:9024548. doi: 10.1155/2022/9024548. eCollection 2022. J Immunol Res. 2022. PMID: 36523350 Free PMC article.
-
Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem-cell phenotype.Br J Dermatol. 2013 Aug;169(2):374-83. doi: 10.1111/bjd.12323. Br J Dermatol. 2013. PMID: 23517330 Free PMC article.
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical