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Radiology Research and Practice
Volume 2012 (2012), Article ID 814396, 6 pages
Sonography of the Primary Cutaneous Melanoma: A Review
Department of Radiology, Clinica Servet, Faculty of Medicine, University of Chile, Almirante Pastene 150, Providencia, Santiago, Chile
Received 28 July 2011; Revised 11 October 2011; Accepted 13 November 2011
Academic Editor: Christiane A. Voit
Copyright © 2012 Ximena Wortsman. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The diagnosis and management of primary cutaneous melanoma have traditionally relied on clinical and histological characteristics. Nevertheless, in recent years there has been a significant growth in the usage of ultrasound for studying the cutaneous layers. Thus, the present paper focuses on the primary lesion, its sonographic characteristics, the potential benefits of early imaging, and the new developments on the ultrasound field applied to cutaneous melanoma.
Cutaneous malignant melanoma constitutes 4 to 11% of all skin cancers but is responsible for more than 75% of skin cancer-related deaths producing more than 8000 deaths per year in the United States . To date the diagnosis is clinical, and the usage of ultrasound in the study of cutaneous melanoma has been focused more on the locoregional staging than on the primary lesion, and the prognosis being mainly assessed by clinical and histological features.
The staging of melanoma is mostly based on the Breslow classification that relies on sequential tumor infiltration (depth) by histology within the different cutaneous layers, providing a measurement of the microscopic invasion from the stratum granulosum of the epidermis to the deepest portion of the tumor . The Breslow index has been reported to correlate well with the prognosis of the disease. Moreover, according to the thickness of the primary tumor, important decisions are taken such as the size of the excision and the free margins or the requirement for a sentinel lymph node procedure.
Nevertheless, there are controversial reports about the appropriate size of the excision that should be performed on melanoma. Hence, a small (but potentially important) difference in overall survival between wide and narrow excision margins has been reported that cannot be confidently ruled out. Literature has mentioned that recurrence-free survival is favored with wide excision (Hazard Ratio 1.13; ; 95% confidence interval 0.99 to 1.28) but the results have not reached statistical significance ( level). Furthermore, randomized trial evidence seems to be insufficient to address optimal excision margins for primary cutaneous melanoma .
Reports on recurrence rates in melanoma have shown a wide range depending on the stage of the primary tumor; thus, they can vary from 7.1% in stage I to 51% in stage III . Moreover, older patients with thicker tumors and angiolymphatic invasion appear to be at higher risk for local and in-transit recurrence . Hence, the appearance of in-transit metastasis seems to be linked to the biological characteristics of the tumor cells rather than an influence of the surgical technique .
Recent advances in ultrasound technology have allowed observation of the cutaneous layers with good resolution. Thus, using multichanneled color Doppler machines, with variable frequency probes that reach frequencies ≥15 MHz, the echostructure of the skin layers can be clearly defined . Furthermore, in spite of the limitations of sonography to detect pigments such as melanin, the noninvasive assessment of the characteristics of the primary tumor, such as thickness and blood flow, may contribute to the modification of critical management decisions.
The literature has sequentially increased sonographic information about primary cutaneous melanoma lesions [7–9]. The first sonographic reports on melanoma were performed using other type of ultrasound equipment that use fixed high-frequency probes that go from 20 to 100 MHz. The usage of these machines provided valuable information that showed a good correlation between sonometry and histometry (), with a mean difference of 0.39 mm (relative difference 28%). This report has also shown that tumors measuring between 0.55 and 0.95 mm thick were incorrectly classified according to histology in 34%. Nevertheless, thicker tumors that measured between 1.30 and 1.70 mm were incorrectly classified in 50% of cases . The latter results may perhaps be related to the low penetration of these fixed frequency ultrasound machines (approximately 6 mm at 20 MHz, 3 mm at 75 MHz, and 1 mm at 100 MZ) [11, 12]. This point could be relevant since the skin presents variable thickness of its layers according to the corporal region; thus, only the dermis could measure more than 3.0 mm (thickness) in normal individuals such as, for example, in the dorsal thoracic region . Nevertheless, the usage of 75 MHz fixed high-frequency ultrasound for observing thin melanomas that presented a mean histological Breslow thickness of 0.4 mm (22 were in situ) showed a high correlation (Pearson’s , ) with a median percentage error up to 13% with the histological Breslow thickness. Sonographic measurements in this report were considered as highly reliable for invasive melanoma, even in the presence of lymphocytic infiltration or nevus .
On the other hand, using multichanneled color Doppler ultrasound equipment with variable frequency probes that go from 10 to 15 MHz, it has already been reported that ultrasound is capable of differentiating melanomas measuring < or >1 mm of thickness, which is important for requiring, for example, a sentinel lymph node procedure that is indicated in melanomas measuring more than 1 mm thick [13, 14].
Thus, recognition of this vital depth information can support the performance of “one-time” surgery in melanoma, where the size of the incision and the free margins as well as the sentinel lymph node procedure are planned with an imaging support presurgically . The use of sonography as a “thickness discriminator” has shown high correlation with histological results [16–18]. Nevertheless, sonographic measurements can be slightly higher than histology because they correspond to in vivo tissue without dehydration or fixation, and may include subtumoral mononuclear infiltrate and nest of nevus cells which cannot be differentiated sonographically from melanoma cells . This small difference in the measurements has been reported to be much less than the actual size of the extension used for assessing the free margins that is usually used in melanoma surgery. Moreover, using 12–15 MHz frequency, the sensitivity and positive predictive values of ultrasound in detecting lesions thicker than 1 mm has been reported to be 92% and 95%, respectively .
Although early stages can be successfully treated by surgery, adjuvant therapies are used for managing advanced states. Furthermore, exceptions to wide local excision include cases where surgical excision may be cosmetically disfiguring or associated with increased morbidity and mortality. Thus, there are several meta-analyses of randomized controlled trials that have reported the impact of adjuvant interferon alfa therapy for malignant melanoma [19–23]. Also, there are systemic therapies such as cytokine therapy, chemotherapy, and biochemotherapy. Additionally, cellular therapy, gene therapy and targeted therapy are undergoing investigation . Furthermore, the role of definitive or adjuvant radiotherapy has largely been relegated to palliative measures. However, the emerging clinical and radiobiological data suggest that many types of effective radiation therapy, such as intensity-modulated radiotherapy for melanoma of the head and neck, and adjuvant radiotherapy for selected high-risk, node-positive patients can improve outcomes . Hence, these nonsurgical treatments may also require noninvasive imaging modalities for objective monitoring of the anatomical changes invisible to the naked eye. Moreover, new applications of ultrasound such as sonodynamic therapy (SDT), that use the energy of ultrasound and certain chemical photocatalyst sensitizers such as Titanium dioxide (TiO2), can be used to kill the cancerous cells in melanoma. So far, this sonication procedure is performed by experimental devices but in the future, perhaps, may be adapted to our usual machines .
2. Sonographic Characteristics of the Primary Melanoma
On sonography, early lesions usually present oval or fusiform shape and hypoechogenicity [27, 28]. Commonly, these lesions infiltrate the dermis and show increased blood flow within the tumor. Nevertheless, cases with in situ lesions may not show detectable masses. In cases with ulcerations, the epidermis may be irregular or discontinuous, and increased echogenicity of the surrounding subcutaneous tissue may also be found . Since the tumor can show asymmetry in its shape, the measurement of thickness should be performed at the deepest point. When examining these lesions, it is recommended to apply a copious amount of gel on the skin surface; thus we can observe the lesion without compressing the vascularity that may present prominent low velocity arterial vessels within the lesions, especially in bulky tumors. Knowledge of the peak systolic arterial velocity of these vessels (cm/sec) may provide an idea of the angiogenic power of the tumor that can correlate with its metastatic potential. Additionally, preoperative ultrasound and guided fine needle aspiration cytology have been reported as useful for identifying sentinel nodes metastasis and reduce the need for surgical sentinel nodes procedures. Moreover, peripheral perfusion has been mentioned as an early sign of involvement and of crucial importance to achieve a high identification rate of metastasis. Balloon shape and loss of central echoes are indeed late signs of malignant nodal infiltration [29, 30]. When studying bulky melanomas, the use of lower frequency probes can help to obtain the complete extension of the tumor which may also require extended field of view capabilities. Of the settings, the power Doppler that is usually more sensitive for detecting slow flow could be more useful than the color Doppler mode. The lowest pulse repetition frequencies (that do not cause aliasing or excessive reduction of the frame rate) and the lowest wall filter and color gain, below the noise threshold, are preferred to obtain better quality images [9, 31] (Figures 1, 2, 3, and 4).
Commonly close to the primary lesion, satellite lesions (arising within 2 cm from the primary tumor) may be found, which may appear as hypoechoic solid masses in the subcutaneous tissue, presenting variable degrees of vascularity [9, 31] (Figure 3).
3. Contrast-Enhanced Ultrasound on Melanoma
Contrast enhanced ultrasound has been progressively more used in the study of the primary lesion and the locoregional metastases. The usage of contrast may support the nonsurgical treatment of the primary lesion and clarify a doubtful cortical thickening at the lymph nodes [32, 33]. Moreover, vascular density has already been correlated with metastatic potential using color Doppler ultrasound. Thus, assessment of the tumor perfusion characteristics is becoming an issue in oncology. Furthermore, neovascularization is a prognostic factor for metastasis equivalent to the Breslow index . Therefore, an early provision of functional images of the primary tumor can provide relevant information concerning the usefulness of new targeted therapies and antiangiogenic treatments, thereby allowing an early assessment of the effectiveness of the treatment [34, 35]. This functional analysis of the tumoral perfusion relies on the acoustic properties of the microbubbles that increase the signal-to-noise ratio and the sensitivity to microvessel detection at higher levels than the power Doppler .
4. Sonoelastography in Cutaneous Melanoma
As yet, few reports that show the usefulness of sonoelastography in cutaneous melanoma are available. To date, the reports are mostly based on acoustooptical elastography (AOE), an experimental imaging modality for quantifying the mechanical behavior of skin lesions. The method relies upon stimulating the tissue with a low-frequency acoustic force and imaging the resulting strains in the tissue by means of quantifying the magnitude of the dynamic shift in a backreflected laser speckle pattern from the skin. The magnitude of the shift reflects the local stiffness of the tissue, which has shown promising results when comparing benign melanocytic nevi with melanoma .
Ultrasound can be a reliable tool for assessing relevant characteristics of the primary lesion such as depth and vascularity. This imaging method is not intended to replace histology but perhaps the anatomical information can provide a missing link between the clinical evaluation, and the later, biopsy and treatments. Furthermore, this detailed data has the potential to help with deciding on appropriate treatment and therefore, may allow a one-time treatment, support an early test of the efficacy of a treatment, and perhaps help to decrease the recurrence rates. Nowadays, considering the fast evolution of imaging technologies, the inclusion of imaging modalities in the routine evaluation and classification of the primary tumors could be the next step to follow in the management of melanomas.
- D. U. Ekwueme, G. Guy, C. Li, S. H. Rim, P. Parelkar, and S. C. Chen, “The health burden and economic costs of cutaneous melanoma mortality by race/ethnicity-United States, 2000 to 2006,” Journal of the American Academy of Dermatology, vol. 65, supplement 1, no. 5, pp. S133–S143, 2011.
- D. T. Netscher, M. Leong, I. Orengo, D. Yang, C. Berg, and B. Krishnan, “Cutaneous malignancies: melanoma and nonmelanoma types,” Plastic and Reconstructive Surgery, vol. 127, no. 3, pp. 37e–56e, 2011.
- M. J. Sladden, C. Balch, D. A. Barzilai et al., “Surgical excision margins for primary cutaneous melanoma,” Cochrane Database of Systematic Reviews, no. 4, p. CD004835, 2009.
- U. Leiter, P. G. Buettner, T. K. Eigentler et al., “Hazard rates for recurrent and secondary cutaneous melanoma: an analysis of 33,384 patients in the German Central Malignant Melanoma Registry,” Journal of the American Academy of Dermatology, vol. 66, no. 1, pp. 37–45, 2012.
- C. C. Stucky, R. J. Gray, A. C. Dueck et al., “Risk factors associated with local and in-transit recurrence of cutaneous melanoma,” American Journal of Surgery, vol. 200, no. 6, pp. 770–774, 2010.
- A. Clemente-Ruiz de Almiron and S. Serrano-Ortega, “Risk factors for in-transit metastasis in patients with cutaneous melanoma,” Actas Dermosifiliogr. In press.
- X. Wortsman and J. Wortsman, “Clinical usefulness of variable-frequency ultrasound in localized lesions of the skin,” Journal of the American Academy of Dermatology, vol. 62, no. 2, pp. 247–256, 2010.
- R. Badea, M. Crişan, M. Lupşor, and L. Fodor, “Diagnosis and characterization of cutaneous tumors using combined ultrasonographic procedures (conventional and high resolution ultrasonography),” Medical Ultrasonography, vol. 12, no. 4, pp. 317–322, 2010.
- O. Catalano, C. Caracò, N. Mozzillo, and A. Siani, “Locoregional spread of cutaneous melanoma: sonography findings,” American Journal of Roentgenology, vol. 194, no. 3, pp. 735–745, 2010.
- J. Tacke, G. Haagen, O. Hornstein et al., “Clinical relevance of sonometry-derived tumour thickness in malignant melanoma—a statistical analysis,” British Journal of Dermatology, vol. 132, no. 2, pp. 209–214, 1995.
- B. D. Fornage, M. H. McGavran, M. Duvic, and C. A. Waldron, “Imaging of the skin with 20-MHz US,” Radiology, vol. 189, no. 1, pp. 69–76, 1993.
- P. Guitera, L. X. Li, K. Crotty et al., “Melanoma histological Breslow thickness predicted by 75-MHz ultrasonography,” British Journal of Dermatology, vol. 159, no. 2, pp. 364–369, 2008.
- R. Vilana, S. Puig, M. Sanchez et al., “Preoperative assessment of cutaneous melanoma thickness using 10-MHz sonography,” American Journal of Roentgenology, vol. 193, no. 3, pp. 639–643, 2009.
- M. M. Mušič, K. Hertl, M. Kadivec, M. D. Pavlović, and M. Hočevar, “Pre-operative ultrasound with a 12-15 MHz linear probe reliably differentiates between melanoma thicker and thinner than 1 mm,” Journal of the European Academy of Dermatology and Venereology, vol. 24, no. 9, pp. 1105–1108, 2010.
- O. Catalano and A. Siani, “Cutaneous melanoma: role of ultrasound in the assessment of locoregional spread,” Current Problems in Diagnostic Radiology, vol. 39, no. 1, pp. 30–36, 2010.
- K. Hoffmann, J. Jung, S. El Gammal, and P. Altmeyer, “Malignant melanoma in 20-MHz B scan sonography,” Dermatology, vol. 185, no. 1, pp. 49–55, 1992.
- D. Jasaitiene, S. Valiukeviciene, G. Linkeviciute, R. Raisutis, E. Jasiuniene, and R. Kazys, “Principles of high-frequency ultrasonography for investigation of skin pathology,” Journal of the European Academy of Dermatology and Venereology, vol. 25, no. 4, pp. 375–382, 2011.
- V. Kaikaris, D. Samsanavičius, K. Maslauskas et al., “Measurement of melanoma thickness—comparison of two methods: ultrasound versus morphology,” Journal of Plastic, Reconstructive and Aesthetic Surgery, vol. 64, no. 6, pp. 796–802, 2011.
- K. Wheatley, N. Ives, B. Hancock, M. Gore, A. Eggermont, and S. Suciu, “Does adjuvant interferon-α for high-risk melanoma provide a worthwhile benefit? A meta-analysis of the randomised trials,” Cancer Treatment Reviews, vol. 29, no. 4, pp. 241–252, 2003.
- D. Pirard, M. Heenen, C. Melot, and P. Vereecken, “Interferon alpha as adjuvant postsurgical treatment of melanoma: a meta-analysis,” Dermatology, vol. 208, no. 1, pp. 43–48, 2004.
- M. B. Lens and M. Dawes, “Interferon alfa therapy for malignant melanoma: a systematic review of randomized controlled trials,” Journal of Clinical Oncology, vol. 20, no. 7, pp. 1818–1825, 2002.
- S. Mocellin, S. Pasquali, C. R. Rossi, and D. Nitti, “Interferon alpha adjuvant therapy in patients with high-risk melanoma: a systematic review and meta-analysis,” Journal of the National Cancer Institute, vol. 102, no. 7, pp. 493–501, 2010.
- A. M. Eggermont, S. Suciu, R. MacKie et al., “Post-surgery adjuvant therapy with intermediate doses of interferon alfa 2b versus observation in patients with stage IIb/III melanoma (EORTC 18952): randomised controlled trial,” Lancet, vol. 366, no. 9492, pp. 1189–1196, 2005.
- J. W. Chang, “Cutaneous melanoma: Taiwan experience and literature review,” Chang Gung Medical Journal, vol. 33, no. 6, pp. 602–612, 2010.
- M. K. Khan, N. Khan, A. Almasan, and R. Macklis, “Future of radiation therapy for malignant melanoma in an era of newer, more effective biological agents,” Journal of OncoTargets and Therapy, vol. 4, pp. 137–148, 2011.
- Y. Harada, K. Ogawa, Y. Irie et al., “Ultrasound activation of TiO2 in melanoma tumors,” Journal of Controlled Release, vol. 20, no. 149, pp. 190–195, 2011.
- N. Lassau, S. Mercier, S. Koscielny et al., “Prognostic value of high-frequency sonography and color Doppler sonography for the preoperative assessment of melanomas,” American Journal of Roentgenology, vol. 172, no. 2, pp. 457–461, 1999.
- N. Lassau, S. Koscielny, M. F. Avril et al., “Prognostic value of angiogenesis evaluated with high-frequency and color doppler sonography for preoperative assessment of melanomas,” American Journal of Roentgenology, vol. 178, no. 6, pp. 1547–1551, 2002.
- C. Voit, A. C. van Akkooi, G. Schäfer-Hesterberg et al., “Ultrasound morphology criteria predict metastatic disease of the sentinel nodes in patients with melanoma,” Journal of Clinical Oncology, vol. 28, no. 5, pp. 847–852, 2010.
- C. A. Voit, A. C. van Akkooi, G. Schäfer-Hesterberg et al., “Rotterdam Criteria for sentinel node (SN) tumor burden and the accuracy of ultrasound (US)-guided fine-needle aspiration cytology (FNAC): can US-guided FNAC replace SN staging in patients with melanoma?” Journal of Clinical Oncology, vol. 27, no. 30, pp. 4994–5000, 2009.
- N. Lassau, A. Spatz, M. F. Avril et al., “Value of high-frequency US for preoperative assessment of skin tumors,” Radiographics, vol. 17, no. 6, pp. 1559–1565, 1997.
- L. Rubaltelli, V. Beltrame, A. Tregnaghi, E. Scagliori, A. C. Frigo, and R. Stramare, “Contrast-enhanced ultrasound for characterizing lymph nodes with focal cortical thickening in patients with cutaneous melanoma,” American Journal of Roentgenology, vol. 196, no. 1, pp. W8–W12, 2011.
- L. Chami, N. Lassau, M. Chebil, and C. Robert, “Imaging of melanoma: Usefulness of ultrasonography before and after contrast injection for diagnosis and early evaluation of treatment,” Clinical, Cosmetic and Investigational Dermatology, vol. 4, pp. 1–6, 2011.
- N. Lassau, L. Chami, M. Chebil et al., “Dynamic contrast-enhanced ultrasonography (DCE-US) and anti-angiogenic treatments,” Discovery Medicine, vol. 11, no. 56, pp. 18–24, 2011.
- N. Lassau, M. Chebil, L. Chami, S. Bidault, E. Girard, and A. Roche, “Dynamic contrast-enhanced ultrasonography (DCE-US): a new tool for the early evaluation of antiangiogenic treatment,” Targeted Oncology, vol. 5, no. 1, pp. 53–58, 2010.
- N. Lassau, L. Chami, B. Benatsou, P. Peronneau, and A. Roche, “Dynamic contrast-enhanced ultrasonography (DCE-US) with quantification of tumor perfusion: a new diagnostic tool to evaluate the early effects of antiangiogenic treatment,” European Radiology, Supplement, vol. 17, supplement 6, pp. F89–F98, 2007.
- S. J. Kirkpatrick, R. K. Wang, D. D. Duncan, M. Kulesz-Martin, and K. Lee, “Imaging the mechanical stiffness of skin lesions by in vivo acousto-optical elastography,” Optics Express, vol. 16, no. 14, pp. 9770–9779, 2006.