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Volgareva G.M.

Blokhin National Medical Research Center of Oncology

Zavalishina L.E.

Russian Medical Academy of Continuous Professional Education

Kuznetsova O.A.

Russian Medical Academy of Continuous Professional Education

Burova O.S.

Blokhin National Medical Research Center of Oncology

Reed nevus and cutaneous melanoma in children: an immunohistochemical study

Authors:

Volgareva G.M., Zavalishina L.E., Kuznetsova O.A., Burova O.S.

More about the authors

Read: 11198 times


To cite this article:

Volgareva GM, Zavalishina LE, Kuznetsova OA, Burova OS. Reed nevus and cutaneous melanoma in children: an immunohistochemical study. Russian Journal of Archive of Pathology. 2021;83(3):30‑34. (In Russ.)
https://doi.org/10.17116/patol20218303130

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References:

  1. Davis LE, Shalin SC, Tackett AJ. Current state of melanoma diagnosis and treatment. Cancer Biol Ther. 2019;20(11):1366-1379. https://doi.org/10.1080/15384047.2019.1640032
  2. Bay SB, Görgün Ö, Kebudi R. Children with malignant melanoma: a single center experience from Turkey. Turk Pediatri Ars. 2020;55(1):39-45.  https://doi.org/10.14744/TurkPediatriArs.2019.90022
  3. Dean PH, Bucevska M, Strahlendorf C, Verchere C. Pediatric melanoma: A 35-year population-based review. Plast Reconstr Surg Glob Open. 2017;5(3):e1252. https://doi.org/10.1097/gox.0000000000001252
  4. Men TKh, Rykov MYu, Polyakov VG. Malignancies in children in Russia: trends and highlights. Russian Journal of Oncology. 2015;20(2):43-47. (In Russ.).
  5. Danysh HE, Navai SA, Scheurer ME, Hunt R, Venkatramani R. Malignant melanoma incidence among children and adolescents in Texas and SEER 13, 1995-2013. Pediatr Blood Cancer. 2019;66(6):e27648. https://doi.org/10.1002/pbc.27648
  6. Averbook BJ, Lee SJ, Delman KA, Gow KW, Zager JS, Sondak VK, Messina JL, Sabel MS, Pittelkow MR, Ecker PM, Markovic SN, Swetter SM, Leachman SA, Testori A, Curiel-Lewandrowski C, Go RS, Jukic DM, Kirkwood JM. Pediatric melanoma: analysis of an international registry. Cancer. 2013;119(22):4012-4019. https://doi.org/10.1002/cncr.28289
  7. Bartenstein DW, Kelleher CM, Friedmann AM, Duncan LM, Tsao H, Sober AJ, Hawryluk EB. Contrasting features of childhood and adolescent melanomas. Pediatr Dermatol. 2018;35(3):354-360.  https://doi.org/10.1111/pde.13454
  8. Reed RJ, Ichinose H, Clark WH Jr, Mihm MC Jr. Common and uncommon melanocytic nevi and borderline melanomas. Semin Oncol. 1975;2(2):119-147. 
  9. Spitz S. Melanomas of childhood. Am J Pathol. 1948;24(3):591-609. 
  10. Pedrosa AF, Lopes JM, Azevedo F, Mota A. Spitz/Reed nevi: a review of clinical-dermatoscopic and histological correlation. Dermatol Pract Concept. 2016;6(2):37-41.  https://doi.org/10.5826/dpc.0602a07
  11. Zhao G, Lee KC, Peacock S, Reisch LM, Knezevich SR, Elder DE, Piepkorn MW, Elmore JG, Barnhill RL. The utilization of spitz-related nomenclature in the histological interpretation of cutaneous melanocytic lesions by practicing pathologists: results from the M-Path study. J Cutan Pathol. 2017;44(1):5-14.  https://doi.org/10.1111/cup.12826
  12. Zhuchkov MV, Bolshakova EE, Sonin DB, Isakov SA, Zhiltsova EE, Masiyanskaya TD. Reed nevus: issues of dermatoscopic diagnosis. Dermatology (Suppl. Consilium Medicum). 2018;1:32-4. (In Russ.).
  13. Dimonitsas E, Liakea A, Sakellariou S, Thymara I, Giannopoulos A, Stratigos A, Soura E, Saetta A, Korkolopoulou P. An update on molecular alterations in melanocytic tumors with emphasis on Spitzoid lesions. Ann Transl Med. 2018;6(12):249.  https://doi.org/10.21037/atm.2018.05.23
  14. Volgareva GM, Lebedeva AV, Polyakov VG. Pigment cell neoplasms in children and adolescens: searching skin melanoma diagnostic markers. Oncopediatrics. 2016;3(1):16-23. (In Russ.).
  15. Volgareva GM, Zavalishina LE, Kazubskaya TP, Senderovich AI, Polyakov VG. Molecular approaches in pediatric pigment skin malformations diagnostics: description of four cases. Oncopediatrics. 2017;4(4):294-400. (In Russ.). https://doi.org/10.15690/onco.v4i4.1816
  16. Sherr CJ. D-type cyclins. Trends Biochem Sci. 1995;20(5):187-190.  https://doi.org/10.1016/s0968-0004(00)89005-2
  17. Bastian BC, LeBoit PE, Hamm H, Bröcker EB, Pinkel D. Chromosomal gains and losses in primary cutaneous melanomas detected by comparative genomic hybridization. Cancer Res. 1998;58(10): 2170-2175.
  18. Gerami P, Jewell SS, Pouryazdanparast P, Wayne JD, Haghighat Z, Busam KJ, Rademaker A, Morrison L. Copy number gains in 11q13 and 8q24 [corrected] are highly linked to prognosis in cutaneous malignant melanoma. J Mol Diagn. 2011;13(3):352-358.  https://doi.org/10.1016/j.jmoldx.2011.01.011
  19. Oba J, Nakahara T, Abe T, Hagihara A, Moroi Y, Furue M. Expression of c-Kit, p-ERK and cyclin D1 in malignant melanoma: an immunohistochemical study and analysis of prognostic value. J Dermatol Sci. 2011;62(2):116-123.  https://doi.org/10.1016/j.jdermsci.2011.02.011
  20. Serrano M, Hannon GJ, Beach D. A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature. 1993;366(6456):704-707.  https://doi.org/10.1038/366704a0
  21. Sherr CJ, Roberts JM. CDK inhibitors: positive and negative regulators of G1-phase progression. Genes Dev. 1999;13(12):1501-1512. https://doi.org/10.1101/gad.13.12.1501
  22. Del Campo AB, Kyte JA, Carretero J, Zinchencko S, Méndez R, González-Aseguinolaza G, Ruiz-Cabello F, Aamdal S, Gaudernack G, Garrido F, Aptsiauri N. Immune escape of cancer cells with beta2-microglobulin loss over the course of metastatic melanoma. Int J Cancer. 2014;134(1):102-113.  https://doi.org/10.1002/ijc.28338

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