Misdiagnosis and Clinical Insights into Acral Amelanotic Melanoma—A Systematic Review

Author:

Cassalia Fortunato1ORCID,Danese Andrea2,Cocchi Enrico345ORCID,Danese Elisabetta2,Ambrogio Francesca6,Cazzato Gerardo7ORCID,Mazza Marcodomenico8ORCID,Zambello Anna1,Belloni Fortina Anna19ORCID,Melandri Davide310ORCID

Affiliation:

1. Unit of Dermatology, Department of Medicine, University of Padova, 35131 Padua, Italy

2. Unit of Dermatology, Department of Medicine, University of Verona, 37134 Verona, Italy

3. Department of Medical and Surgical Sciences, University of Bologna, 40126 Bologna, Italy

4. Department of Precision Medicine and Genomics, Department of Medicine, Columbia University, New York, NY 10027, USA

5. Neonatal and Pediatric Intensive Care Unit, AUSL Romagna, 47121 Forlì, Italy

6. Section of Dermatology and Venereology, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari “Aldo Moro”, 70124 Bari, Italy

7. Section of Molecular Pathology, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari “Aldo Moro”, 70124 Bari, Italy

8. Soft-Tissue, Peritoneum and Melanoma Surgical Oncology Unit, Veneto Institute of Oncology IOV-IRCCS, 35128 Padova, Italy

9. Regional Center for Pediatric Dermatology, Department of Women’s, and Children’s Health (SDB), University of Padua, 35121 Padua, Italy

10. Cesena Skin Clinic and Regional Skin Bank, AUSL Romagna, 47121 Forlì, Italy

Abstract

Background: Acral amelanotic melanomas (AAMs), a rare subset of melanomas located on acral sites such as the palms, soles, and subungual areas, are diagnostically challenging due to their lack of typical pigmentation and often benign clinical appearance. Misdiagnosis is common, leading to delays in treatment and potentially worse outcomes. This systematic review aims to synthesise evidence on cases of AAM initially misdiagnosed as other conditions, to better understand their clinical and epidemiological characteristics, diagnostic pitfalls, and management strategies. Methods: A comprehensive search of the MEDLINE/PubMed, EMBASE, and SCOPUS databases was conducted up to March 2024. Case reports and small case series of AAMs initially misdiagnosed as other conditions were included. Data on patient demographics, clinical presentation, and diagnostic methods were collected and analyzed. Results: Of the 152 records identified, 26 cases from 23 articles met the inclusion criteria. A demographic analysis revealed that the gender distribution appears to be perfectly balanced, with an age range of 38 to 91 years. Misdiagnoses included non-healing ulcers or traumatic lesions (37.5%), benign proliferative lesions (29.2%) and infectious lesions (20.8%). The foot was the most affected site (53.8%). Notably, a histological evaluation was performed in 50% of cases involving the upper extremities, in contrast to only 7.1% of cases involving the foot and 0% of cases of the heel. This discrepancy suggests a reluctance to perform biopsies in the lower extremities, which may contribute to a higher misdiagnosis rate in these areas. Conclusions: The underutilization of biopsy in the diagnosis of lower extremity lesions contributes significantly to the misdiagnosis and delay in treatment of AAMs. Especially when the clinical assessment and dermoscopy are inconclusive, biopsies of suspicious lesions are essential. Immunohistochemistry and markers such as PRAME are critical in differentiating melanoma from other malignancies such as clear cell sarcoma. This review highlights the need for increased vigilance and a proactive diagnostic approach to increase early detection rates and improve prognostic outcomes.

Publisher

MDPI AG

Reference47 articles.

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2. Amelanotic acral melanoma misdiagnosed as verruca plantaris;Deng;An. Bras. Dermatol.,2019

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4. Amelanotic melanoma;Gong;Melanoma Res.,2019

5. Acral Amelanotic Melanoma Mimicking a Foot Ulcer;Shawa;Cureus,2022

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