Tumores melanocíticos

  1. Muñoz Moreno-Arrones, O. 1
  2. Jaén Olasolo, P. 1
  1. 1 Departamento de Dermatología. Hospital Universitario Ramón y Cajal. Madrid. España
Journal:
Medicine: Programa de Formación Médica Continuada Acreditado

ISSN: 0304-5412

Year of publication: 2022

Issue Title: Enfermedades de la piel (I)

Series: 13

Issue: 47

Pages: 2735-2744

Type: Article

DOI: 10.1016/J.MED.2022.01.003 DIALNET GOOGLE SCHOLAR

More publications in: Medicine: Programa de Formación Médica Continuada Acreditado

Abstract

The most relevant melanocytic tumors are melanocytic nevi, commonly called «moles», which are the consequence of the migration and later proliferation of cells of neuroectodermal origin to the skin. Though they can be congenital, they are mostly acquired; one of the main determinants of their appearance is sun exposure. Despite the fact that it is an intensely debated issue, it is accepted that skin melanomas (malignant proliferations of melanocytes) only come from melanocytic nevi in one-third of cases; the majority appear de novo. The treatment and prognosis for skin melanomas has undergone a revolution in the past decade due to the advent of targeted therapy and immunotherapy. In localized forms of melanoma, complete extirpation of the lesion with widening continues to be the gold standard treatment, as a cure is possible with this method. In locally advanced forms (for example, lymph node invasion), adjuvant medical treatment has been praised for increasing disease-free time. In stage IV melanomas or those with distant metastases, systemic immunotherapy and targeted anti-BRAF/MEK therapy has entirely supplanted classical chemotherapy, as it significantly prolongs patients’ life expectancy.

Bibliographic References

  • Schaffer JV. Update on melanocytic nevi in children. Clin Dermatol. 2015;33:368.
  • Orlow I, Satagopan JM, Berwick M, Enriquez HL, White KA, Cheung K. Genetic factors associated with naevus count and dermoscopic patterns: preliminary results from the Study of Nevi in Children (SONIC). Br J Dermatol. 2015;172(4):1081-93.
  • Oliveria SA, Satagopan JM, Geller AC, Dusza SW, Weinstock MA, Berwick M. Study of NEVI IN CHILDREN (SONIC): baseline findings and predictors of nevus count. Am J Epidemiol. 2009;169(1):41-53.
  • Aalborg J, Morelli JG, Mokrohisky ST, Asdigian NL, Byers TE, Dellavalle RP. Tanning and increased nevus development in very light skinned children without red hair. Arch Dermatol. 2009;145(9):989-96.
  • Schaffer JV. Pigmented lesions in children: when to worry. Curr Opin Pediatr. 2007 Aug;19(4):430-40.
  • Luther H, Altmeyer P, Garbe C, Ellwanger U, Jahn S, Hoffmann K. Increase of melanocytic nevus counts in children during 5 years of follow-up and analysis of associated factors. Arch Dermatol. 1996;132(12):1473-8.
  • Garbe C, Büttner P, Weiss J, Soyer HP, Stocker U, Krüger S, et al. Associated factors in the prevalence of more than 50 common melanocytic nevi, atypical melanocytic nevi, and actinic lentigines: multicenter case-control study of the Central Malignant Melanoma Registry of the German Dermatological Society. J Invest Dermatol. 1994;102(5):700-5.
  • Dellavalle RP, Johnson KR, Hester EJ, Deas AM, Mokrohisky S, Morelli JG. Children with red hair have more freckles but fewer melanocytic nevi: results from a cohort study of 280 three-year-olds. Arch Dermatol. 2005;141(8):1042-3.
  • Slade J, Marghoob AA, Salopek TG, Rigel DS, Kopf AW, Bart RS. Atypical mole syndrome: risk factor for cutaneous malignant melanoma and implications for management. J Am Acad Dermatol. 1995;32(3):479-94
  • Granter SR, McKee PH, Calonje E, Mihm MC Jr, Busam K. Melanoma associated with blue nevus and melanoma mimicking cellular blue nevus: a clinicopathologic study of 10 cases on the spectrum of so called ‘malignant blue nevus’. Am J Surg Pathol. 2001;25:316-23.
  • Aloi F, Pich A, Pippione M. Malignant cellular blue nevus: a clinicopathological study of 6 cases. Dermatology. 1996;192:36-40.
  • Sau P, Graham JH, Helwig EB. Pigmented spindle cell nevus: a clinicopathologic analysis of ninety-five cases. J Am Acad Dermatol. 1993;28:565-71.
  • Tlougan BE, Orlow SJ, Schaffer JV. Spitz nevi: beliefs, behaviors, and experiences of pediatric dermatologists. JAMA Dermatol. 2013;149:283-91.
  • Argenziano G, Agozzino M, Bonifazi E, Broganelli P, Brunetti B, Ferrara G. Natural evolution of Spitz nevi. Dermatology. 2011;222:56-60.
  • Kanada KN, Merin MR, Munden A, Friedlander SF. A prospective study of cutaneous findings in newborns in the United States: correlation with race, ethnicity, and gestational status using updated classification and nomenclature. J Pediatr. 2012;161:240-5.
  • Castilla EE, da Graça Dutra M, Orioli-Parreiras IM. Epidemiology of congenital pigmented naevi: I. Incidence rates and relative frequencies. Br J Dermatol. 1981;104:307-15.
  • Tannous ZS, Mihm MC Jr, Sober AJ, Duncan LM. Congenital melanocytic nevi: clinical and histopathologic features, risk of melanoma, and clinical management. J Am Acad Dermatol. 2005;52:197-203.
  • Price HN, Schaffer JV. Congenital melanocytic nevi-when to worry and how to treat: Facts and controversies. Clin Dermatol. 2010;28:293.
  • Precursors to malignant melanoma. National Institutes of Health Consensus Development Conference Statement, Oct. 24-26, 1983. J Am Acad Dermatol. 1984;10:683.
  • Rabinovitz HS, Barnhill RL. Benign melanocytic neoplasms. En: Bolognia JL, Jorizzo JL, Schaffer JV, eds. Dermatology. 3ª ed. Philadelphia: Elsevier-Saunders; 2012.
  • Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin. 2019;69(1):7-34.
  • Balch CM, Soong SJ, Gershenwald JE, Thompson JF, Reintgen DS, Cascinelli N, et al. Prognostic factors analysis of 17,600 melanoma patients: validation of the American Joint Committee on Cancer melanoma staging system. J Clin Oncol. 2001;19(16):3622-34
  • Geller AC, Miller DR, Annas GD, Demierre MF, Gilchrest BA, Koh HK. Melanoma incidence and mortality among US whites, 1969-1999. JAMA. 2002;288(14):1719-20.
  • Breslow A. Thickness, cross-sectional areas and depth of invasion in the prognosis of cutaneous melanoma. Ann Surg. 1970;172:902-8.
  • Paek SC, Sober AJ, Tsao H. Cutaneous melanoma. En: Wolff K, Goldsmith LA, Katz SI, eds. Fitzpatrick’s dermatology in general medicine. vol. 1. 7ª ed. New York: McGraw Hill Medical; 2008. p. 1134.
  • Pampena R, Kyrgidis A, Lallas A, Moscarella E, Argenziano G, Longo C. A meta-analysis of nevus-associated melanoma: Prevalence and practical implications. J Am Acad Dermatol. 2017 Nov;77(5): 938-45.
  • Geller AC, Elwood M, Swetter SM, Brooks DR, Aitken J, Youl PH. Factors related to the presentation of thin and thick nodular melanoma from a population-based cancer registry in Queensland Australia. Cancer. 2009;115:1318-27.
  • Esteva A, Kuprel B, Novoa RA, Ko J, Swetter SM, Blau HM, et al. Dermatologist-level classification of skin cancer with deep neural networks. Nature. 2017;542:115-8.
  • Marsden JR, Newton Bishop JA, Burrows L, Cook M, Corrie PG, Cox NH. Revised U.K. guidelines for the management of cutaneous melanoma 2010. Br J Dermatol. 2010;163:238-56.
  • Coit DG, Andtbacka R, Anker CJ, Bichakjian CK, Carson WE 3rd. Melanoma, version 2.2013: featured updates to the NCCN guidelines. J Natl Compr Canc Netw. 2013;11:395-407.
  • Swetter SM, Tsao H, Bichakjian CK, Curiel Lewandrowski C, Elder DE, Gershenwald JE. Guidelines of care for the mana- gement of primary cutaneous melanoma. J Am Acad Dermatol. 2019;80:208-50.
  • Piepkorn MW, Longton GM, Reisch LM, Elder DE, Pepe MS, Kerr KF. Assessment of second-opinion strategies for diagnoses of cutaneous melanocytic lesions. JAMA Netw Open. 2019;2:e1912597.