Journal Logo

Research Article: Observational Study

Initial misdiagnosis of melanoma located on the foot is associated with poorer prognosis

Sondermann, Wiebke MD; Zimmer, Lisa MD; Schadendorf, Dirk MD; Roesch, Alexander MD; Klode, Joachim MD; Dissemond, Joachim MD

Editor(s): Issa., Fadi

Author Information
doi: 10.1097/MD.0000000000004332


1 Introduction

Melanoma has become a growing interdisciplinary problem in public health worldwide. According to the World Health Organization (WHO), the incidence of melanoma is increasing faster than any other cancer in the world. Melanoma is the third most common cancer in Australia and the fifth in the United States of America (USA). The American Cancer Society estimated that about 70,230 new melanomas were diagnosed in the USA in 2011, resulting in about 8790 deaths.[1] Although melanoma accounts for less than 5% of skin cancer cases, it causes more than 75% of skin cancer deaths[2] and, thus, represents a significant health issue and economic burden.[3,4] It is well known that a high tumor thickness (Breslow depth), the histological ulceration state of the primary melanoma and increased mitotic rate are associated with a poorer prognosis.[5] Up to 15% of all cutaneous melanomas are localized at the foot and ankle. Moreover melanoma is the most common neoplasm seen at feet.[6]

The WHO distinguishes 4 main histopathological subtypes of melanoma: superficial spreading malignant melanoma (SSM), nodular malignant melanoma (NMM), lentigo maligna melanoma (LMM), and acrolentiginous malignant melanoma (ALM).[7,8] ALMs show special histological characteristics and are often equated with melanoma in acral localizations.[9] About 1% to 7% of all cutaneous melanomas in Caucasians are ALM.[10] In Asians, Africans, and the Middle Eastern population, ALM shows a significantly higher prevalence as compared to Caucasians and accounts for up to 70% of all melanomas.[11,12] Several studies demonstrated a poorer prognosis of ALM in comparison to melanomas of other localizations.[13,14] It has been discussed that this is mainly attributed to the prolonged diagnosis of ALM. The delay in diagnosis may be caused by the relative inaccessibility of the feet for self-assessment. In addition, many common skin diseases like fungal infections, warts, hematoma, or chronic wounds (e.g., in diabetes) appear at the feet and can lead to misdiagnoses. Therefore, the aim of our study was to analyze the rate and duration of misdiagnosis in patients with melanoma located on the foot and to characterize the clinical consequences.

2 Methods

2.1 Identification of patients

A prospective, computerized melanoma database at the Skin Cancer Center of the University Hospital Essen, Germany was used to identify patients with histologically confirmed melanoma located on the foot which were diagnosed between 2002 and July 2013.

Patients with acral melanomas localized at other body sites, including the hand, were excluded from the cohort as well as patients exhibiting acral melanoma metastases. Tumors were categorized as ALM or NM which were the most frequent histological subgroups. Rarer subtypes as well as samples lacking classification were grouped together in the group other. Misdiagnoses and previous treatments were identified by medical history.

This prospective, observational study was approved by the Institutional Review Board of the University of Duisburg-Essen (IRB protocol number 12-4961-BO). All patients included in the study provided written informed consent. Patient written consent was also granted for medical images published in the study.

2.2 Statistical evaluation

The statistical analysis was performed with SPSS (Statistical Package for Social Science, SPSS, Inc., Chicago, IL) version 22. The Chi-square test or Fisher exact test were used to evaluate relationships between categorical variables. Kaplan–Meier plots and the log-rank test were used to evaluate the relationship between the diagnosis (initially correct diagnosis vs misdiagnosis) and the outcome starting from the date of surgical melanoma resection to the date of first disease recurrence or death or the last follow-up visit, respectively. The association between misdiagnosis, Breslow depth, histology, sex, local recurrence, age, and ulceration as prognostic factors was analyzed for the clinical outcome by univariate analysis and stepwise multivariate Cox-regression analysis. Hazard ratios and 95% confidence intervals (CIs) were calculated from the Cox-regression model including all factors for multivariate analysis as a 2-sided test. Differences were regarded significant at P < 0.05.

3 Results

3.1 Patient characteristics and main results

A cohort of 151 patients with acral melanoma located on the foot was identified of whom 107 patients qualified for subsequent analysis (cf. Supplemental STROBE flow diagram, Forty-two patients were male (39.3%) and 65 (60.7%) were female. The female to male ratio was 1:1.6. The mean age at first diagnosis was 61.6 years (median 66 years). The youngest patient was 19 years, the oldest 88 years old. The tumor thickness varied between 0.1 and 20 mm (mean 2.4 mm, median 1.6 mm). A significant difference in tumor thickness was seen between patients with an initial misdiagnosis (mean 3.7 mm, median 3.1 mm) and patients with an initially correct diagnosis (mean 1.9 mm, median 1.1 mm) (P = 0.001). 39.3% of all melanomas (n = 42) were ulcerated (Table 1).

Table 1
Table 1:
Patient characteristics.

3.2 Misdiagnoses and first clinical signs

In 32 of the 107 patients (30%, 18 females, 14 males), skin lesions at the feet were incorrectly diagnosed at the first medical visit. The median age for patients who were initially misdiagnosed was 63.5 years (range 29–83 years) compared with a median age of 68 years for initially correctly diagnosed patients (range 19–88 years). The most frequent misdiagnoses were wounds including diabetic foot ulcers, traumas, and peripheral arterial occlusive disease in nearly 50% of the cases (15 out of 32 patients, Table 2).

Table 2
Table 2:
Misdiagnoses and corresponding number of patients.

At the first visit, patients typically presented with common symptoms such as painless new lesions or macules with changing color or ulcerations which were mostly interpreted as trauma or wounds (Table 3).

Table 3
Table 3:
First clinical symptoms and corresponding number of patients.

3.3 Tumor stage at initial diagnosis of melanoma

In 104 of the 107 patients, information on the tumor stage was available at initial diagnosis of melanoma. Overall, 80 patients (76.9%) presented with local tumor disease, that is, primary melanomas up to stage IIC according to the American Joint Committee on Cancer (AJCC) 2009 classification; 24 patients (23.1%) had already developed advanced disease with lymph node and/or organ metastases (AJCC stage III–IV).[15]

Fifty-nine (80.8%) of the patients with an initially correct diagnosis at the first clinical visit (n = 73) were in a localized stage (AJCC stage I–II), while 14 cases (19.2%) showed advanced disease (AJCC stage III–IV). In contrast, 32.3% of the cases with an initially incorrect diagnosis (n = 31) already showed regional or distant tumor progression (AJCC stage III–IV). However, this difference was not statistically significant (P = 0.2).

3.4 Delay in diagnosis

Information on the exact time span between the first recognized symptoms and the date of melanoma diagnosis was available for 102 out of 107 patients. The median interval between the first clinical signs and the date of melanoma diagnosis was 138 days (0 to 6570 days). In the cohort of initially correctly diagnosed patients, the time span between first symptoms and melanoma diagnosis ranged between 0 and 3650 days (median 92 days). For patients with an initial misdiagnosis, the median diagnostic interval was 365 days (ranging from 91 up to 6570 days, P = 0.004). In patients with ulcerated melanomas, the median time span for correct diagnosis was 365 days (7–6570 days). Without ulceration, the median interval between first symptoms and melanoma diagnosis was significantly reduced to 92 days (0–3650 days, P = 0.02). In male patients, the time span from the first clinical symptoms until diagnosis of melanoma was 121 days (range 0–3650 days), in females 214 days (0–6570 days, P = 0.37).

3.5 Disease-free and overall survival

The median patient follow-up was 26.8 months (0–320.8 months). The median observational time for the misdiagnosis cohort was 34.1 months (0–184 months) and for the correctly diagnosed cohort 18.7 months (0.7–320.8 months). The disease-free survival rate and overall survival rate were analyzed for the dependency on correct or incorrect melanoma diagnosis using Kaplan–Meier survival curves (Fig. 1). Table 4 provides a summary of prognostic factors for the overall survival rate by univariate and multivariate analyses. Only the parameter “misdiagnosis” represented a statistically significant indicator for reduced survival in both the univariate (95% CI: 1.34–9.54, P = 0.01) and multivariate analysis (95% CI: 1.37–9.99, P = 0.01). The calculated 5-year disease-free survival rate was 47.8% in the misdiagnosis cohort versus 72.7% in the correctly diagnosed cohort (P = 0.02). The 5-year overall survival rates were 63.5% (misdiagnosis cohort) and 88.4% (correctly diagnosed cohort; P = 0.007, Fig. 1). The calculated overall survival rate for the whole cohort was 85.1%.

Figure 1
Figure 1:
Calculated 5-year overall survival rate for the correctly diagnosed cohort versus the initially misdiagnosed cohort.
Table 4
Table 4:
Univariate and multivariate analysis of overall survival.

4 Discussion

To the best of our knowledge, this is one of the largest studies on misdiagnosis of melanoma located on the foot. Our results demonstrate a median delay of melanoma diagnosis by approximately 9 months, when skin lesions on the foot have been misdiagnosed at the first medical visit. Melanomas of misdiagnosed patients showed significantly increased Breslow depth and a higher rate of ulceration than patients with an earlier diagnosis. In addition, we demonstrated that an initial misdiagnosis was associated with poorer prognosis regarding 5-year disease-free survival rate and 5-year overall survival rate.

4.1 Misdiagnoses and first clinical signs

In our study, 30% of the melanomas were incorrectly diagnosed at the first medical visit. This is in line with the results of other groups.[14,16,17] For example, Fortin et al[14] found an initial misdiagnosis rate of 25%, while Bristow and Acland[16] reported a rate of incorrect diagnosis of 33%. Thus, melanomas of the feet seem to be more frequently misdiagnosed as compared to melanomas from other body sites where the overall misdiagnosis rate is approximately 10%.[18,19] However, there are also reports on errors in diagnosis of melanomas not only located at the foot. For example, a recent study by Simionescu et al analyzed errors in approaches to melanoma. Among 30 patients, 36 clinical diagnostic errors were made (multiple errors were possible).[20]

In our cohort, the percentage of melanomas located on the foot misclassified as wounds was higher as compared to the other studies (Soon et al[17]: 11% wounds, Bristow and Acland[16]: 14% wounds). The most frequently observed clinical presentation of melanomas in our study was a new patch or a change in color of a preexisting lesion. An increase in size of a preexisting lesion was the second most common symptom reported by our patients while it was the most frequent symptom in the study by Bristow and Acland.[16] In the series of Bristow and Acland[16] a change of color was reported by 2 of 21 patients. Bleeding was the third most common symptom in our study and the second most reported in the study by Bristow and Acland.[16]

4.2 Tumor types

ALM was the most frequent tumor type in our study, diagnosed in 36.4% of our patients. In other studies, the frequency of ALM ranged from 29% to 67% in melanomas located at hands and feet.[17,21–24]

4.3 Tumor thickness and ulceration state

The mean tumor thickness for all patients of our study was 2.4 mm (median tumor thickness 1.6 mm), which is lower as compared to Fortin et al[14] who reported a mean tumor thickness of 3.0 mm and Soon et al[17] who reported a mean of 3.3 mm. The mean tumor thickness in patients with initial misdiagnosis in our study was 3.7 mm (median tumor thickness 3.1 mm) and, thus, significantly higher in comparison to patients with a correct diagnosis of melanoma (mean 1.9 mm, median 1.1 mm). Comparable data were reported by Bennett et al[24] who found a mean tumor thickness for initially correct diagnosis of 2.2 mm versus 3.8 mm for patients with initial misdiagnosis. With 4.3 mm, Fortin et al[14] reported an even higher mean thickness for misdiagnosed melanoma in their cohort.

Regarding all body sites, the median Breslow depth at first diagnosis in Germany is about 0.9 mm (mean 1.66 mm).[3,25]

In our series, we found ulcerations in 39.3% of the tumors. This is comparable to the rate of ulceration of 36% showed by Phan et al[23] in a large histopathological investigation of 121 patients.

4.4 Tumor stage at initial diagnosis and delay in diagnosis

Overall 76.9% of the melanomas of our study were classified as local disease. Current data from the melanoma register in Tübingen, Germany indicate that 88.6% of all melanomas are diagnosed in AJCC stage I–II.[3] The median delay in melanoma diagnosis of 9 months found in our study was slightly shorter as compared to results from other studies. For example, Metzger et al[19] found a mean delay in diagnosis of 12 months for palmoplantar melanoma and of about 18 months for subungual melanoma. Bristow and Acland[16] reported an average delay of 13.5 months.

4.5 Data on survival and prognostic factors

Our results suggest that the 5-year disease-free survival rate as well as the overall survival rate is significantly reduced in patients with misdiagnosis of melanoma located on the foot. The calculated 5-year overall survival rates were 63.5% in the misdiagnosis cohort versus 88.4% in the correctly diagnosed cohort.

In the study of Metzger et al[19] the estimated 5-year survival rate for initially correctly diagnosed subungual melanoma was 90.9% and 68.5% for misdiagnosed cases. However, in their study, melanomas of the hand were also included. Kuchelmeister et al[13] found a 5-year survival rate of 71% for ALM irrespective of the body site, while Phan et al[26] reported a 5-year survival rate of 76% for a similar cohort. However, Phan and Kuchelmeister did not differentiate between initially correctly classified lesions and misdiagnosed lesions.

Only the factor “misdiagnosis” was identified in our study as statistically significant independent factor for prediction of overall survival. Unexpectedly, the histological tumor thickness was no significant discriminator. This observation is confirmed by several other studies.[27,28] For example, Phan et al explained this paradox by a lower accuracy of histological tumor assessment in acral tumor locations due to the artificial fragmentation during surgical excision. Additionally, the histological tumor measurement could be less accurate in such locations because inappropriate surgical procedure are often conducted before the final excision and diagnosis.[23]

4.6 Reasons for high misdiagnosis rate in melanoma located on the foot

Cutaneous melanoma represents a tumor entity that can be early detected, by visual (self-) examination. However, considering an average age for first diagnosis of ALM of 60 to 70 years, self-examination is not always feasible due to physical limitations of the patients (reduced eyesight and mobility). Also professional examination of the tight interdigital space is hampered by limited accessibility, in particular for dermatoscopes. Furthermore, the commonly used “ABCDE” rule for self-examination is not applicable to most ALMs due to the lack of typical clinical features of pigment tumors when located at glabrous skin.[16] In addition, many common skin diseases like hematoma, fungal infections, warts, or chronic wounds frequently appear at the feet and can mimic melanoma.

4.7 Relevance for the clinical routine

One characteristic of our study was the high rate of melanomas located on the foot which were initially misdiagnosed as wounds in the context of diabetic foot syndrome, peripheral occlusive arterial disease, posttraumatic ulcer, or unknown etiology. Because of the high prevalence of these diseases, especially diabetic foot syndrome and peripheral occlusive arterial disease, there is a high likelihood of misinterpretation of melanomas as wounds. It should be taken into account that a complete reepithelialization of wounds at the feet may take longer than 8 weeks. Nonetheless, there should be a healing tendency under adequate therapy. If this is not the case, a biopsy should be taken to histologically rule out malignancy at a maximum after 8 weeks.[29–31] Lesions which are suspicious for melanoma from the beginning should be analyzed histologically as soon as possible.

4.8 Strengths and weaknesses of the study

The large sample size enabled us to perform an extensive analysis of the clinical misdiagnosis of melanoma located on the foot and the influence on the clinical course and survival of the patients. We have included only melanoma on the feet but not the hands, which are known to have a better prognosis because of a usually earlier recognition.

Our study results may be biased by the specialized set-up of our wound care department and, thus, patient recruitment for this study. As part of a university setting, we see selected therapy-refractory cases. This could be a confounding factor with regard to a higher rate of ulceration and more advanced tumor stages.

In sum, melanomas located on the foot represent diagnostic pitfalls (Fig. 2). Difficulties in (self-) examination and the occurrence of common benign differential diagnoses at this particular body site promote a considerable delay in diagnosis resulting in a poorer prognosis. In order to reduce any delay in diagnosis, we suggest a diagnostic algorithm with basic instructions also for nondermatologists for the assessment of unclear skin lesions located on the foot (Fig. 3).

Figure 2
Figure 2:
Melanoma located on the foot initially misdiagnosed as a fungal infection.
Figure 3
Figure 3:
Flow chart for the diagnosis of melanoma located on the foot.


1. American Cancer Society. Cancer Facts & Figures 2011. Available at: Accessed February 23, 2016.
2. American Cancer Society. Cancer Facts & Figures 2010. Available at: Accessed February 23, 2016.
3. Livingstone E, Windemuth-Kieselbach C, Eigentler TK, et al A first prospective population-based analysis investigating the actual practice of melanoma diagnosis, treatment and follow-up. Eur J Cancer 2011; 4713:1977–1989.
4. Hill VK, Gartner JJ, Samuels Y, et al The genetics of melanoma: recent advances. Annu Rev Genomics Hum Genet 2013; 14:257–279.
5. Garbe C, Hauschild A, Volkenandt M, et al Evidence and interdisciplinary consense-based German guidelines: diagnosis and surveillance of melanoma. Melanoma Res 2007; 176:393–399.
6. Barnes BC, Seigler HF, Saxby TS, et al Melanoma of the foot. J Bone Joint Surg Am 1994; 766:892–898.
7. Clark WH Jr, Mihm MC Jr. Lentigo maligna and lentigo-maligna melanoma. Am J Pathol 1969; 551:39–67.
8. Smoller BR. Histologic criteria for diagnosing primary cutaneous malignant melanoma. Mod Pathol 2006; 19 (suppl 2):S34–S40.
9. Durbec F, Martin L, Derancourt C, et al Melanoma of the hand and foot: epidemiological, prognostic and genetic features. A systematic review. Br J Dermatol 2012; 1664:727–739.
10. Ridgeway CA, Hieken TJ, Ronan SG, et al Acral lentiginous melanoma. Arch Surg 1995; 1301:88–92.
11. Chang JW, Yeh KY, Wang CH, et al Malignant melanoma in Taiwan: a prognostic study of 181 cases. Melanoma Res 2004; 146:537–541.
12. Hudson DA, Krige JE. Melanoma in black South Africans. J Am Coll Surg 1995; 1801:65–71.
13. Kuchelmeister C, Schaumburg-Lever G, Garbe C. Acral cutaneous melanoma in Caucasians: clinical features, histopathology and prognosis in 112 patients. Br J Dermatol 2000; 1432:275–280.
14. Fortin PT, Freiberg AA, Rees R, et al Malignant melanoma of the foot and ankle. J Bone Joint Surg Am 1995; 779:1396–1403.
15. Balch CM, Gershenwald JE, Soong SJ, et al Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol 2009; 2736:6199–6206.
16. Bristow IR, Acland K. Acral lentiginous melanoma of the foot and ankle: a case series and review of the literature. J Foot Ankle Res 2008; 11:11
17. Soon SL, Solomon AR Jr, Papadopoulos D, et al Acral lentiginous melanoma mimicking benign disease: the Emory experience. J Am Acad Dermatol 2003; 482:183–188.
18. Krige JE, Isaacs S, Hudson DA, et al Delay in the diagnosis of cutaneous malignant melanoma. A prospective study in 250 patients. Cancer 1991; 689:2064–2068.
19. Metzger S, Ellwanger U, Stroebel W, et al Extent and consequences of physician delay in the diagnosis of acral melanoma. Melanoma Res 1998; 82:181–186.
20. Simionescu O, Blum A, Grigore M, et al Learning from mistakes: errors in approaches to melanoma and the urgent need for updated national guidelines. Int J Dermatol 2015; doi: 10.1111/ijd.13165. [Epub ahead of print].
21. Feibleman CE, Stoll H, Maize JC. Melanomas of the palm, sole, and nailbed: a clinicopathologic study. Cancer 1980; 4611:2492–2504.
22. Hughes LE, Horgan K, Taylor BA, et al Malignant melanoma of the hand and foot: diagnosis and management. Br J Surg 1985; 7210:811–815.
23. Phan A, Touzet S, Dalle S, et al Acral lentiginous melanoma: histopathological prognostic features of 121 cases. Br J Dermatol 2007; 1572:311–318.
24. Bennett DR, Wasson D, MacArthur JD, et al The effect of misdiagnosis and delay in diagnosis on clinical outcome in melanomas of the foot. J Am Coll Surg 1994; 1793:279–284.
25. Livingstone E, Krajewski C, Eigentler TK, et al Prospective evaluation of follow-up in melanoma patients in Germany—results of a multicentre and longitudinal study. Eur J Cancer 2015; 515:653–667.
26. Phan A, Touzet S, Dalle S, et al Acral lentiginous melanoma: a clinicoprognostic study of 126 cases. Br J Dermatol 2006; 1553:561–569.
27. Slingluff CL Jr, Vollmer R, Seigler HF. Acral melanoma: a review of 185 patients with identification of prognostic variables. J Surg Oncol 1990; 452:91–98.
28. O’Leary JA, Berend KR, Johnson JL, et al Subungual melanoma. A review of 93 cases with identification of prognostic variables. Clin Orthop Relat Res 2000; 378:206–212.
29. Ruttermann M, Maier-Hasselmann A, Nink-Grebe B, et al Local treatment of chronic wounds: in patients with peripheral vascular disease, chronic venous insufficiency, and diabetes. Dtsch Arztebl Int 2013; 1103:25–31.
30. Senet P, Combemale P, Debure C, et al Malignancy and chronic leg ulcers: the value of systematic wound biopsies: a prospective, multicenter, cross-sectional study. Arch Dermatol 2012; 1486:704–708.
31. Reich-Schupke S, Doerler M, Wollina U, et al Squamous cell carcinomas in chronic venous leg ulcers. Data of the German Marjolin Registry and review. J Dtsch Dermatol Ges 2015; 1310:1006–1013.

chronic wound; disease-free survival; foot; malignant melanoma; misdiagnosis; prognosis; overall survival rate

Supplemental Digital Content

Copyright © 2016 The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.