Soft Tissue Sarcoma Mimicking Melanoma: A Systematic Review

Author:

Cassalia Fortunato1ORCID,Cavallin Francesco2ORCID,Danese Andrea3,Del Fiore Paolo4ORCID,Di Prata Claudia5,Rastrelli Marco45,Belloni Fortina Anna6ORCID,Mocellin Simone45

Affiliation:

1. Unit of Dermatology, Department of Medicine, University of Padua, 35121 Padua, Italy

2. Independent Researcher, 36020 Solagna, Italy

3. Unit of Dermatology, Department of Integrated Medical and General Activity, University of Verona, 37100 Verona, Italy

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

5. Department of Surgical, Oncological and Gastroenterological Sciences (DISCOG), University of Padua, 35128 Padua, Italy

6. Pediatric Dermatology Unit, Department of Medicine DIMED, University of Padua, 35121 Padua, Italy

Abstract

Background: Sarcoma may show similarities to malignant melanoma in terms of morphologic and immunohistochemical aspects, making it difficult to differentiate between these two neoplasms during the diagnostic process. This systematic review aims to summarize available evidence on cases of sarcoma that were initially diagnosed as melanoma. Methods: A comprehensive search of the MEDLINE/Pubmed, EMBASE, and SCOPUS databases was conducted through March 2023. We included case series and case reports of sarcoma patients that were initially diagnosed as malignant melanoma. PRISMA guidelines were followed. Results: Twenty-three case reports and four case series with a total of 34 patients were included. The clinical presentation was heterogeneous, and the most involved anatomical regions were lower limbs (24%), head/neck (24%), and upper limbs (21%). IHC positivity was reported for S100 (69%), HMB45 (63%), MelanA (31%), and MiTF (3%). The main reasons for a second assessment were unusual presentation (48%) and uncertain diagnosis (28%). EWSR1 translocation was investigated in 17/34 patients (50%) and found to be positive in 16/17 (94%). The final diagnosis was clear cell sarcoma (50%) or other soft tissue sarcomas (50%). Conclusions: Melanoma and some histotypes of sarcoma share many similarities. In cases of atypical lesions, a second diagnosis should be considered, and ESWR1 translocation should be investigated.

Funder

Italian Ministry of Health

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference41 articles.

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3. (2023, April 10). American Cancer Society Key Statistics for Soft Tissue Sarcomas. Available online: https://www.cancer.org/cancer/soft-tissue-sarcoma/about/key-statistics.html.

4. Clear cell sarcoma of soft tissue: A clinicopathologic, immunohistochemical, and molecular analysis of 33 cases;Hisaoka;Am. J. Surg. Pathol.,2008

5. Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses);Panagopoulos;Cancer Genet. Cytogenet.,2005

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