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Dermoscopic features of thin melanomas: a comparative study of melanoma in situ and invasive melanomas smaller than or equal to 1mm* * Work conducted at the University Hospital of the Federal University of Santa Catarina (HU-UFSC) - Florianópolis (SC), Brazil

Características dermatoscópicas de melanomas finos: estudo comparativo entre melanomas in situ e melanomas invasivos menores ou iguais a 1mm

Abstracts

BACKGROUND:

Dermoscopy allows the early detection of melanomas. The preoperative determination of Breslow index by dermoscopy could be useful in planning the surgical approach and in selecting patients for sentinel lymph node biopsy.

OBJECTIVES:

This study aims at describing the dermoscopic features of thin melanomas and comparing melanomas in situ with invasive melanomas less than or equal to 1 mm thick.

METHODS:

This was an observational retrospective study in which the dermoscopy photographs of 41 thin melanomas were evaluated. Three observers evaluated together 14 dermoscopic criteria.

RESULTS:

Among thin melanomas, the most frequent criteria were presence of asymmetry in two axes in 95% of cases (39 cases), 3 or more colors in 80.4% of cases (33 cases), atypical dots or globules in 58.5% of cases (24 cases) and atypical network or streaks in 53.6% of cases (22 cases). The group of invasive melanomas presented with a higher frequency and statistical significance (p <0.05) 3 or more colors (OR: 16.1), milky red areas (OR: 4.8) and blue-white veil (OR: 20.4), and a greater tendency to have streaks or atypical network (OR: 3.66).

CONCLUSIONS:

Thin melanomas tend to have asymmetry in the two axes, 3 or more colors, atypical dots or globules and atypical network or streaks. Melanomas in situ tend to have up to 2 colors, no blue-white veil and no milky red area. Invasive melanomas tend to have 3 or more colors, a milky red area, blue-white veil, and atypical network or streaks. Further studies are needed to confirm these findings.

Dermoscopy; Melanoma; Skin neoplasms


FUNDAMENTOS:

A dermatoscopia propicia o diagnóstico mais precoce do melanoma. A estimativa préoperatória da espessura de Breslow através da dermatoscopia poderia ser útil no planejamento da conduta cirúrgica e seleção dos pacientes para a biópsia de linfonodo sentinela.

OBJETIVOS:

Este estudo objetiva descrever as características dermatoscópicas encontradas em melanomas finos e comparar melanomas in situ com melanomas invasivos menores ou iguais a 1 mm.

MÉTODOS:

Trata-se de estudo observacional, retrospectivo, no qual avaliouse o registro fotográfico da dermatoscopia de 41 melanomas finos. Três observadores avaliaram em conjunto 14 critérios dermatoscópicos.

RESULTADOS:

Dentre os melanomas finos, os critérios mais encontrados foram: presença de assimetria nos dois eixos em 95% (39 casos), 3 ou mais cores em 80,4% (33 casos), pontos ou glóbulos atípicos em 58,5% (24 casos) e rede atípica ou estrias radiadas em 53,6% (22 casos). O grupo dos melanomas invasivos apresentou com maior frequência e significância estatística (p<0,05) a presença de 3 ou mais cores (OR: 16,1), áreas vermelho-leitosas (OR: 4,8) e véu (OR: 20,4), além de uma maior tendência em apresentar rede atípica ou estrias radiadas (OR: 3,66).

CONCLUSÕES:

Os melanomas finos tendem a apresentar assimetria nos dois eixos, 3 ou mais cores, pontos ou glóbulos atípicos e rede atípica ou estrias radiadas. Os melanomas in situ tendem a apresentar até 2 cores, ausência de véu e de área vermelho-leitosa. Os melanomas invasivos tendem a exibir 3 cores ou mais, área vermelho-leitosa, véu, rede atípica ou estrias radiadas. Outros estudos são necessários para a confirmação dos achados.

Dermoscopia; Melanoma; Neoplasias cutâneas


INTRODUCTION

Melanoma is an aggressive skin cancer. Even though it is highly mortal, it can be curable and its prognosis can be considered good if the disease is detected at an early stage.11. Brasil. Ministério da Saúde. Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA). Estimativa 2012: incidência de câncer no Brasil. Rio de Janeiro: INCA; 2011. p. 49-50. [acesso 24 Jun 2011]. Disponível em: http://www.inca.gov.br/estimativa/2012/index.asp?ID=1
http://www.inca.gov.br/estimativa/2012/i...
It affects mainly Caucasians, although this type of cancer affects all ethnic groups at different rates.11. Brasil. Ministério da Saúde. Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA). Estimativa 2012: incidência de câncer no Brasil. Rio de Janeiro: INCA; 2011. p. 49-50. [acesso 24 Jun 2011]. Disponível em: http://www.inca.gov.br/estimativa/2012/index.asp?ID=1
http://www.inca.gov.br/estimativa/2012/i...
It is estimated that in 2012 the incidence of melanoma in Brazil was 3,170 new cases in men and 3,060 in women.11. Brasil. Ministério da Saúde. Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA). Estimativa 2012: incidência de câncer no Brasil. Rio de Janeiro: INCA; 2011. p. 49-50. [acesso 24 Jun 2011]. Disponível em: http://www.inca.gov.br/estimativa/2012/index.asp?ID=1
http://www.inca.gov.br/estimativa/2012/i...
The highest estimated rates are found in the South region of the country.11. Brasil. Ministério da Saúde. Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA). Estimativa 2012: incidência de câncer no Brasil. Rio de Janeiro: INCA; 2011. p. 49-50. [acesso 24 Jun 2011]. Disponível em: http://www.inca.gov.br/estimativa/2012/index.asp?ID=1
http://www.inca.gov.br/estimativa/2012/i...
Therefore, studies of the population of this region are of great value.

Considering that current therapies against advanced melanoma are not very effective, early diagnosis and intervention are valuable to reduce mortality. Dermoscopy is a noninvasive technique that allows the visualization of structures in vivo, from the epidermis to the papillary dermis, that are not seen with the naked eye. Dermoscopy is more accurate than clinical examination; it increases sensitivity in up to 10-27%, making the earlier detection of melanoma possible.22. Bafounta ML, Beauchet A, Aegerter P, Saiag P. Is dermoscopy (epiluminescence microscopy) useful for the diagnosis of melanoma? Results of a meta-analysis using techniques adapted to the evaluation of diagnostic tests. Arch Dermatol. 2001;137:1343-50. , 33. Mayer J. Systematic review of the diagnostic accuracy of dermatoscopy in detecting malignant melanoma. Med J Aust. 1997;167:206-10. Besides increasing diagnostic accuracy, it reduces the rate of excision of benign lesions that may be similar to melanoma when seen with the naked eye.44. Argenziano G, Cerroni L, Zalaudek I, Staibano S, Hofmann-Wellenhof R, Arpaia N, et al. Accuracy in melanoma detection: A 10-year multicenter survey. J Am Acad Dermatol. 2012;67:54-9.

In 1970, Breslow described a simple method to measure the depth of melanoma invasion by means of pathological examination.55. Breslow A. Thickness, cross-sectional areas and depth of invasion in the prognosis of cutaneous melanoma. Ann Surg. 1970;172:902-8. The Breslow index is still the simplest and most useful single variable related to prognosis.66. Elder DE. Thin melanoma. Arch Pathol Lab Med. 2011;135:342-6. The current staging system for melanoma of the American Joint Committee on Cancer uses the Breslow index as the primary attribute of classification. It applies a cut-off of 1.0 mm instead of the initial cut-off of 0.76 mm used by Breslow.55. Breslow A. Thickness, cross-sectional areas and depth of invasion in the prognosis of cutaneous melanoma. Ann Surg. 1970;172:902-8. , 77. Balch CM, Gershenwald JE, Soong SJ, Thompson JF, Atkins MB, Byrd DR, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol. 2009;27:6199-206. Melanomas up to 1 mm thick are defined as thin melanomas because they have a good prognosis, with an 85 to 90%77. Balch CM, Gershenwald JE, Soong SJ, Thompson JF, Atkins MB, Byrd DR, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol. 2009;27:6199-206. chance of a 10-year-survival after surgical excision with a margin of 1 cm.88. NIH Consensus conference. Diagnosis and treatment of early melanoma. JAMA. 1992;268:1314-9.

Thin melanomas include melanomas in situ and invasive melanomas with a depth less than or equal to 1 mm. Melanoma in situ is a diagnostic entity surgically treated with 0.5 cm margins, and there have been no deaths resulting from melanomas in situ that were properly excised.88. NIH Consensus conference. Diagnosis and treatment of early melanoma. JAMA. 1992;268:1314-9. These same surgical margins are recommended in Brazil by the Brazilian Melanoma Group.99. GBM.org [Internet]. Conduta terapêutica no Melanoma. [acesso 24 Jun 2011]. Disponível em: http://www.gbm.org.br/GBM/socios.aspx
http://www.gbm.org.br/GBM/socios.aspx...
Moreover, the Breslow index is one of the criteria used in selecting patients for sentinel lymph node biopsy (SLNB).99. GBM.org [Internet]. Conduta terapêutica no Melanoma. [acesso 24 Jun 2011]. Disponível em: http://www.gbm.org.br/GBM/socios.aspx
http://www.gbm.org.br/GBM/socios.aspx...
, 1010. Boland GM, Gershenwald JE. Sentinel lymph node biopsy in melanoma. Cancer J. 2012;18:185-91. Whenever possible, SLNB is recommended before wide excision of the primary tumor to minimize destruction of the lymphatic vessels.1111. Gannon CJ, Rousseau DL Jr, Ross MI, Johnson MM, Lee JE, Mansfield PF, et al. Accuracy of lymphatic mapping and sentinel lymph node biopsy after previous wide local excision in patients with primary melanoma. Cancer. 2006;107:2647-52. Recognition of thin melanomas is also important considering that elective lymph node dissections and extensive staging evaluations are not recommended for patients with thin melanoma.88. NIH Consensus conference. Diagnosis and treatment of early melanoma. JAMA. 1992;268:1314-9.

Preoperative assessment of the Breslow index by dermoscopy and knowledge of the dermoscopic features of thin melanomas may be important in planning the surgical approach and in selecting patients for SLNB at the time of tumor excision. This study aims at describing the dermoscopic features of thin melanomas and evaluating whether there are differences between melanomas in situ and invasive melanomas less than or equal to 1 mm thick. No similar Brazilian studies have been found in the literature.

MATERIALS AND METHODS

This was an observational retrospective study. The study included a convenience sample, and the digital photographic record of the dermoscopic images of 41 thin melanomas (less than or equal to 1 mm thick) was evaluated, totaling 35 patients, dated from 2006 to March 2012. All the patients seen at the Outpatient Clinic of Dermoscopy and Melanoma (Hospital University, Federal University of Santa Catarina) with at least one diagnosis of thin melanoma were considered for data collection. The data were collected from 2011 to March 2012. Patients who did not have a photographic record prior to excisional biopsy, whose record was not adequate or who had undergone an incisional biopsy before the photographic record were excluded from the study. Due to the dermoscopic characteristics of the so-called specials areas (scalp, face, palms, soles and mucous membranes), only lesions in the neck, trunk and limbs were included.

All dermoscopic images were obtained using the Heine Delta 20® Dermatoscope (Heine®, Germany), with alcohol-gel as linkage fluid. A Nikon UR-E15® adapter (Nikon®, Japan) was used to connect to a Nikon® E8400 camera (Nikon®, Japan). In cases of large lesions that could not be included in only one photographic field, multiple images of different areas were obtained to record all tumor areas. Three different observers, blinded to the Breslow index, analyzed the images.

Data such as sex, age, Breslow index and histological type were collected. Through observation of the lesion on the computer, the observers agreed with regard to the presence or absence of the following criteria: asymmetry in 1 or 2 axes, atypical network, streaks, atypical dots, atypical globules, pseudopods, blotches, blue-white veil, structureless area, atypical vessels, milky red area, island, peppering and white scar-like area. For more objectivity, atypical network and streaks were grouped into the same criterion, as well as atypical dots and atypical globules. When there was an island, its type was also noted. The dermatoscopic features associated with the diagnosis of melanoma in this work have been described in previous studies (Table 1).1212. Argenziano G, Soyer HP, Chimenti S, Talamini R, Corona R, Sera F, et al. Dermoscopy of pigmented skin lesions: results of a consensus meeting via the Internet. J Am Acad Dermatol. 2003;48:679-93.

13. Borsari S, Longo C, Ferrari C, Benati E, Bassoli S, Schianchi S, et al. Dermoscopic island: a new descriptor for thin melanoma. Arch Dermatol. 2010;146:1257-62.

14. Argenziano G, Zalaudek I, Corona R, Sera F, Cicale L, Petrillo G, et al. Vascular structures in skin tumors: a dermoscopy study. Arch Dermatol. 2004;140:1485-9.

15. Soyer HP, Argenziano G, Chimenti S, Ruocco V. Dermoscopy of pigmented skin lesions. Eur J Dermatol. 2001;11:270-6.
- 1616. Stolz W, Semmelmayer U, Johow K, Burgdorf WHC. Principles of dermatoscopy of pigmented skin lesions. Semin Cutan Med Surg. 2003;22:9-20. The SPSS (Statistical Package for Social Sciences) version 17.0 was used in the statistical analysis, with a confidence interval of 95% and statistical significance of p <0.05. To assess the differences between groups, the chi-square test was applied. For variables with fewer than 5 events, Fisher's exact test was used to calculate p. Considering variables for which no event was observed, the value for the calculation of p and OR (odds ratio) was 0.5.

Table 1
Definitions of the dermoscopic criteria used in the study

Ethical aspects

This study was approved by the Human Research Ethics Committee of the Federal University of Santa Catarina under certificate number 893 and was conducted according to the principles of the Declaration of Helsinki.

RESULTS

Forty-one (41) thin melanomas were evaluated. They were identified in 35 patients (14 men and 21 women), with a mean age of 57.1 years (24-86 years). Seventeen cases were of melanoma in situ (41.5%). The average thickness of melanomas, when invasive, was 0.47 mm (standard deviation of 0.2). Of the total, 75% of invasive melanomas had a Breslow index of up to 0.53 mm. Thirty-seven lesions were classified as superficial spreading. The other melanomas (5 cases), all in situ, were of the lentigo maligna type.

With regard to the analyzed dermoscopic structures, the following criteria were more frequently observed in all thin melanomas (in situ and invasive): presence of asymmetry in two axes in 95% of cases (39 cases), 3 or more colors in 80.4 % of cases (33 cases), atypical dots or globules in 58.5% of cases (24 cases) and atypical network or streaks in 53.6% of cases (22 cases). The least frequent structures were blotches in 2.4% of cases (1 case), pseudopods in 4.9% of cases (2 cases) and island in 7.3% of cases (3 cases). All cases of island were of the reticular type. Table 2 details the frequency of each criterion by group: melanomas in situ, invasive melanomas less than or equal to 1 mm thick, and the set of all melanomas. Considerable differences were found between the first two groups. The group of invasive melanomas presented with greater frequency and statistical significance (p <0.05) 3 or more colors (OR: 16.1), milky red areas (OR: 4.8) and blue-white veil (OR: 20.4). Atypical network or streaks tend to be more frequent in the group of invasive melanomas (OR: 3.66). Regarding the other characteristics analyzed, there were no differences between the groups.

Table 2
Frequency of the analyzed criteria in all melanomas and in melanomas in situ and invasive melanomas less than or equal to 1 mm thick

Figure 1 shows the dermoscopic characteristics found in melanomas in situ, while figures 2 and 3 show the characteristics observed in invasive melanomas less than 1 mm thick.

FIGURE 1
Lentigo maligna melanoma in situ on the foot. Dermoscopy shows asymmetry in two axes, two colors, atypical dots and globules and structureless area
FIGURE 2
Superficial spreading melanoma with a Breslow index of 0.5 mm in the cervical region. Dermoscopy shows asymmetry in two axes, four colors, atypical globules, streaks, and milky red area
FIGURE 3
Superficial spreading melanoma with a Breslow index of 0.9 mm on the forearm. Dermoscopy shows asymmetry in two axes, 4 colors, atypical network, streaks, atypical dots and globules, bluewhite veil, and multiple blue-gray dots

DISCUSSION

The Breslow index is a simple and objective measure. Since it is the most useful criterion related to prognosis, it determines surgical margins and the selection of patients for SLNB. Preoperative assessment of the Breslow index using noninvasive methods has been the subject of previous studies.1717. Guitera P, Li LX, Crotty K, Fitzgerald P, Mellenbergh R, Pellacani G, et al. Melanoma histological Breslow thickness predicted by 75-MHz ultrasonography. Br J Dermatol. 2008;159:364-9.

18. Argenziano G, Fabbrocini G, Carli P, De Giorgi V, Delfino M. Epiluminescence microscopy: criteria of cutaneous melanoma progression. J Am Acad Dermatol. 1997;37:68-74.

19. Lorentzen HF, Weismann K, Larsen FG. Dermatoscopic prediction of melanoma thickness using latent trait analysis and likelihood ratios. Acta Derm Venereol. 2001;81:38-41.

20. Hayashi K, Koga H, Uhara H, Saida T. High-frequency 30-MHz sonography in preoperative assessment of tumor thickness of primary melanoma: usefulness in determination of surgical margin and indication for sentinel lymph node biopsy. Int J Clin Oncol. 2009;14:426-30.

21. Argenziano G, Fabbrocini G, Carli P, De Giorgi V, Delfino M. Clinical and dermatoscopic criteria for the preoperative evaluation of cutaneous melanoma thickness. J Am Acad Dermatol. 1999;40:61-8.

22. Carli P, de Giorgi V, Palli D, Giannotti V, Giannotti B. Preoperative assessment of melanoma thickness by ABCD score of dermatoscopy. J Am Acad Dermatol. 2000;43:459-66.
- 2323. Stante M, De Giorgi V, Cappugi P, Giannotti B, Carli P. Non-invasive analysis of melanoma thickness by means of dermoscopy: a retrospective study. Melanoma Res. 2001;11:147-52. According to the literature, melanomas <0.76 mm show a pigmented network more frequently than thicker melanomas, and melanomas >0.76 mm more frequently exhibit atypical vessels and blue-gray areas.1818. Argenziano G, Fabbrocini G, Carli P, De Giorgi V, Delfino M. Epiluminescence microscopy: criteria of cutaneous melanoma progression. J Am Acad Dermatol. 1997;37:68-74. , 1919. Lorentzen HF, Weismann K, Larsen FG. Dermatoscopic prediction of melanoma thickness using latent trait analysis and likelihood ratios. Acta Derm Venereol. 2001;81:38-41. , 2121. Argenziano G, Fabbrocini G, Carli P, De Giorgi V, Delfino M. Clinical and dermatoscopic criteria for the preoperative evaluation of cutaneous melanoma thickness. J Am Acad Dermatol. 1999;40:61-8.

All the thin melanomas in our study showed asymmetry in two axes, 3 or more colors, atypical dots or atypical globules and atypical network or streaks. Asymmetry in two axes is described as a criterion found in 96% of malignant melanomas, which is consistent with our findings, even though our assessment included only thin melanomas.2424. Stolz W, Braun-Falco O, Bilek P, Landthaler M, Burgdorf W, Cognetta A. Atlas Colorido de Dermatoscopia. 2 ed. Rio de Janeiro: DiLivros; 2002.

Streaks were also found in these melanomas by Gkalpakiotis, who, upon assessing 71 thin melanomas, found streaks in 68 cases.2525. Gkalpakiotis S, Arenbergerova M, Arenberger P, Sefrnova P. Dermoscopic features of thin melanomas. J Am Acad Dermatol. 2012;66:AB83. Some authors have shown that the presence of atypical irregular network is more related to early melanomas (<1 mm).1919. Lorentzen HF, Weismann K, Larsen FG. Dermatoscopic prediction of melanoma thickness using latent trait analysis and likelihood ratios. Acta Derm Venereol. 2001;81:38-41. , 2323. Stante M, De Giorgi V, Cappugi P, Giannotti B, Carli P. Non-invasive analysis of melanoma thickness by means of dermoscopy: a retrospective study. Melanoma Res. 2001;11:147-52. In 2001, Stante studied 84 cases of melanomas of all thickness. The author found a correlation between Breslow index and dermoscopic criteria, verifying that the presence of atypical network is more associated with early melanomas, being found in 88% of melanomas in situ.2323. Stante M, De Giorgi V, Cappugi P, Giannotti B, Carli P. Non-invasive analysis of melanoma thickness by means of dermoscopy: a retrospective study. Melanoma Res. 2001;11:147-52. In our study, this criterion is well observed when all thin melanomas are considered, but it is interesting to note that it is less frequent in melanomas in situ when compared to invasive melanomas less than or equal to 1 mm thick. Perhaps this tendency could be confirmed by studying a larger sample, observing statistical significance.

Another interesting finding is the difference in the number of colors found in both groups. It is known that all melanomas show 3 or more colors in 85% of cases and five or more colors in 40% of cases.2424. Stolz W, Braun-Falco O, Bilek P, Landthaler M, Burgdorf W, Cognetta A. Atlas Colorido de Dermatoscopia. 2 ed. Rio de Janeiro: DiLivros; 2002. In our study we observed that the higher the number of colors, the greater the possibility that the lesion is invasive, with a 16-fold increased risk if 3 or more colors are found.

Although dermoscopic islands have been described as a characteristic associated with thin melanomas arising from a nevus, in our study the presence of dermoscopic islands in thin melanomas was less frequent. It is important to note that only approximately 25% of melanomas arise from a pre-existing nevus.1313. Borsari S, Longo C, Ferrari C, Benati E, Bassoli S, Schianchi S, et al. Dermoscopic island: a new descriptor for thin melanoma. Arch Dermatol. 2010;146:1257-62. , 2626. Stolz W, Schmoeckel C, Landthaler M, Braun-Falco O. Association of early malignant melanoma with nevocytic nevi. Cancer. 1989;63:550-5.

Several authors have shown that atypical vessels are rarely found in thin melanomas.1818. Argenziano G, Fabbrocini G, Carli P, De Giorgi V, Delfino M. Epiluminescence microscopy: criteria of cutaneous melanoma progression. J Am Acad Dermatol. 1997;37:68-74. , 1919. Lorentzen HF, Weismann K, Larsen FG. Dermatoscopic prediction of melanoma thickness using latent trait analysis and likelihood ratios. Acta Derm Venereol. 2001;81:38-41. , 2121. Argenziano G, Fabbrocini G, Carli P, De Giorgi V, Delfino M. Clinical and dermatoscopic criteria for the preoperative evaluation of cutaneous melanoma thickness. J Am Acad Dermatol. 1999;40:61-8. , 2525. Gkalpakiotis S, Arenbergerova M, Arenberger P, Sefrnova P. Dermoscopic features of thin melanomas. J Am Acad Dermatol. 2012;66:AB83. We have found atypical vessels in 31.7% of thin melanomas. We believe that it is more difficult to assess this criterion retrospectively, considering that most studies use contact dermoscopy to examine the lesions, and contact can compress the vessels and lead to an impaired record during this process.

Our study also shows that invasive melanomas present with a blue-white veil and milky red area more often than melanomas in situ, showing statistical significance. The blue-white veil is a structure that shows tumor nests in the dermis associated with orthokeratosis, acanthosis and hypergranulosis, and is more commonly associated with thick melanomas.1515. Soyer HP, Argenziano G, Chimenti S, Ruocco V. Dermoscopy of pigmented skin lesions. Eur J Dermatol. 2001;11:270-6. The milky red area appears due to the increased vascularity of the tumor and, although rarely seen, it is the vascular structure with the highest predictive value for the diagnosis of melanoma (77.8%).1414. Argenziano G, Zalaudek I, Corona R, Sera F, Cicale L, Petrillo G, et al. Vascular structures in skin tumors: a dermoscopy study. Arch Dermatol. 2004;140:1485-9.

Regression structures, like peppering and white scar-like areas, are less observed in thin melanomas, which is in agreement with our findings (less than 10% of thin melanomas showed regression structures).1818. Argenziano G, Fabbrocini G, Carli P, De Giorgi V, Delfino M. Epiluminescence microscopy: criteria of cutaneous melanoma progression. J Am Acad Dermatol. 1997;37:68-74. , 1919. Lorentzen HF, Weismann K, Larsen FG. Dermatoscopic prediction of melanoma thickness using latent trait analysis and likelihood ratios. Acta Derm Venereol. 2001;81:38-41. , 2323. Stante M, De Giorgi V, Cappugi P, Giannotti B, Carli P. Non-invasive analysis of melanoma thickness by means of dermoscopy: a retrospective study. Melanoma Res. 2001;11:147-52. Seidenari et al. evaluated regression structures (blue areas and/or peppering and/or veil and/or white scar-like areas) in 255 melanocytic lesions; they observed these characteristics in benign lesions and also in melanomas in situ and invasive melanomas.2727. Seidenari S, Ferrari C, Borsari S, Benati E, Ponti G, Bassoli S, et al. Reticular greyblue areas of regression as a dermoscopic marker of melanoma in situ. Br J Dermatol. 2010;163:302-9. However, this study showed that regression is not only more frequent and extensive in invasive melanomas than it is in in situ lesions, but it also has a different morphological expression. While in invasive lesions areas without blue-gray structures usually related to veil and white scar-like area - are frequently observed, in melanoma in situ the disappearance of the network or of dermoscopic structures in circumscribed regions of the lesion gives rise to areas of light brown pigmentation without structures.

Important considerations about the results of this study have to be made. It is relvant to stress that, although significant, some results showed a great confidence interval, which is mainly related to the sample size. Furthermore, this study did not include lesions with a Breslow index greater than 1 mm. Studies that include thicker melanomas would be useful to assess the specificity of the characteristics of thin melanomas and corroborate these findings. Prospective studies, evaluated by different groups of observers, are needed to confirm the reproducibility and validity of these diagnostic criteria.

CONCLUSION

This study showed that some dermoscopic features may be associated with Breslow index. In general, thin melanomas mainly present asymmetry in two axes, 3 or more colors, atypical dots or atypical globules and atypical network or streaks. Melanomas in situ tend to have up to 2 colors, no blue-white veil and no milky red area. Invasive melanomas tend to exhibit 3 or more colors, a milky red area, blue-white veil, atypical network or streaks. Dermoscopic evaluation plays an important role in diagnostic accuracy, but it can also be used to estimate preoperative thickness. Other prospective, multicentered studies of a larger sample and that include thick melanomas are needed to confirm these findings.

REFERENCES

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    Bafounta ML, Beauchet A, Aegerter P, Saiag P. Is dermoscopy (epiluminescence microscopy) useful for the diagnosis of melanoma? Results of a meta-analysis using techniques adapted to the evaluation of diagnostic tests. Arch Dermatol. 2001;137:1343-50.
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    Mayer J. Systematic review of the diagnostic accuracy of dermatoscopy in detecting malignant melanoma. Med J Aust. 1997;167:206-10.
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    Argenziano G, Cerroni L, Zalaudek I, Staibano S, Hofmann-Wellenhof R, Arpaia N, et al. Accuracy in melanoma detection: A 10-year multicenter survey. J Am Acad Dermatol. 2012;67:54-9.
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  • Financial Support: None
  • *
    Work conducted at the University Hospital of the Federal University of Santa Catarina (HU-UFSC) - Florianópolis (SC), Brazil

Publication Dates

  • Publication in this collection
    Oct 2013

History

  • Received
    26 July 2012
  • Accepted
    28 Oct 2012
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