Biomicroscopia Ultrassônica - Um aliado no diagnóstico da metástase no melanoma - estudo em animais
DOI:
https://doi.org/10.29384/rbfm.2015.v9.n3.p10-14Abstract
O melanoma é o tipo mais agressivo de câncer de pele. A agressividade no melanoma se caracteriza por sua capacidade metastática, e esta agressividade está diretamente relacionada ao diagnóstico tardio. A técnica utilizada neste trabalho foi a biomicroscopia ultrassônica (BMU) – ultrassom de alta frequência - com o objetivo de diagnosticar, de forma não invasiva, em tempo real, o processo de metástase das células de melanoma do tumor primário para o linfonodo sentinela (LFS), em um estudo longitudinal. Neste estudo observou-se fenômenos biológicos ao longo do tempo, como a angiogênese, migração e invasão das células de melanoma no LFS. Concluímos que a BMU pode ser uma útil ferramenta, oferecendo antes da biópsia do LFS, relevantes informações quanto à metástase, possibilitando o início precoce do tratamento, podendo aumentar significativamente a sobrevida do paciente.
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References
Maverakis E, Cornelius LA, Bowen GM, Phan T, Patel FB, Fitzmaurice S, et al. Metastatic Melanoma - A Review of Current and Future Treatment Options. Acta Derm Venereol. 2014. doi: 10.2340/00015555-2035.
Sandru A, Voinea S, Panaitescu E, Blidaru A. Survival rates of patients with metastatic malignant melanoma. Journal of Medicine and Life. 2014; (7):572-6.
Byrom L, Olsen C, Knight L, Khosrotehrani K, Green AC. Increased mortality for pregnancy-associated melanoma: systematic review and meta-analysis. J Eur Acad Dermatol Venereol. 2015. doi: 10.1111/jdv.12972.
Tsao H, Olazagasti JM, Cordoro KM, Brewer JD, Taylor SC, Bordeaux JS, et al. Early detection of melanoma: Reviewing the ABCDEs. J Am Acad Dermatol. 2015. doi: 10.1016/j.jaad.2015.01.025.
Chernoff KA, Marghoob AA, Lacouture ME, Deng L, Busam KJ, Myskowski PL. Dermoscopic Finding in Cutaneous metastases. JAMA Dermatol. 2014; (4):429-33.
Kardynal A, Olszewska M. Modern non-invasions diagnostic techniques in the detection of early cutaneous melanoma. J Dermatol Case Rep. 2014; (1):1-8.
Foster FS, Zhang MY, Zhou YQ, Liu G, Mehi J, Cherin E, et al. A new ultrasound instrument for in vivo microimaging of mice. Ultrasound Med Biol. 2002; (9):1165-72.
Turnbull DH, Ramsay JA, Shivji GS, Bloomfield TS, From L, Sauder DN,et al. Ultrasound backscatter microscope analysis of mouse melanoma progression. Ultrasound Med Biol. 1996; (7):845-53.
Jasaitiene D, Valiukeviciene S, Linkeviciute G, Raisutis R, Jasiuniene E, Kazys R. Principles of high-frequency ultrasonography for investigation of skin pathology. J Eur Acad Dermatol Venereol. 2011; (4):375-82. 10. Phan GQ, Messina JL, Sondak VK, Zager JS. Sentinel lymph node biopsy for melanoma: indications and rationale. Cancer Control. 2009 Jul;16(3):234-9. 11. Pereira ER, Jones D, Jung K, Padera TP. The lymph node microenvironment and its role in the progression of metastatic cancer. Semin Cell Dev Biol. 2015; (38):98-105. 12. Nathanson SD, Shah R, Rosso K. Sentinel lymph node metastases in cancer: causes, detection and their role in disease progression. Semin Cell Dev Biol. 2015; (38):106-16. 13. Joyce KM, McInerney NM, Joyce CW, Jones DM, Hussey AJ, Donnellan P, et al. A review of sentinel lymph node biopsy for thin melanoma. Ir J Med Sci. 2015; (1):119-23. 14. Bennett JJ. Sentinel Lymph Node Biopsy for Breast Cancer and Melanoma. 2006; (3);22-24. 15. Diller ML, Martin BM, Delman KA. Lymph node dissection for stage III melanoma. Surg Oncol Clin N Am. 2015; (2):261-77. 16. Abbas O, Miller DD, Bhawan J. Cutaneous malignant melanoma: update on diagnostic and prognostic biomarkers. Am J Dermatopathol. 2014; (5):363-79.
Peixinho CC, Martins NS, de Oliveira LF, Machado JC. Reliability of measurements of rat lateral gastrocnemius architectural parameters obtained from ultrasound biomicroscopic images. PLoS One. 2014; doi: 10.1371/journal.pone.0087691. 18. Petrella LI, Valle HA, Issa PR, Martins CJ, Pereira WC, Machado JC. Study of cutaneous cell carcinomas ex vivo using ultrasound biomicroscopic images. Skin Res Technol. 2010; (4):422-7.
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