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A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand
Malignant melanoma is relatively uncommon and accounts for 1%–3% of all malignant tumors. Malignant melanoma of the hand is exceptionally rare and highly malignant, with rapid progression if left untreated. Early clinical symptoms can be overlooked, and the tumor is often at a late stage when patien...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10264841/ https://www.ncbi.nlm.nih.gov/pubmed/37323976 http://dx.doi.org/10.1016/j.jhsg.2023.01.015 |
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author | Anthony, Taylor Goodman, Aubree Fan, Juston Gnass, Ronaldo D. Sherman, Christopher L. Thomson, Bryon |
author_facet | Anthony, Taylor Goodman, Aubree Fan, Juston Gnass, Ronaldo D. Sherman, Christopher L. Thomson, Bryon |
author_sort | Anthony, Taylor |
collection | PubMed |
description | Malignant melanoma is relatively uncommon and accounts for 1%–3% of all malignant tumors. Malignant melanoma of the hand is exceptionally rare and highly malignant, with rapid progression if left untreated. Early clinical symptoms can be overlooked, and the tumor is often at a late stage when patients seek care, prompting amputation of the affected region. We present a case of a 48-year-old man who presented with a rapidly progressive, large, fungating mass of the distal aspect of the little finger diagnosed as malignant melanoma. We describe the presentation and treatment of this patient, who ultimately underwent partial amputation of the fifth metacarpal. Histologic analysis demonstrated nodular melanoma. |
format | Online Article Text |
id | pubmed-10264841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102648412023-06-15 A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand Anthony, Taylor Goodman, Aubree Fan, Juston Gnass, Ronaldo D. Sherman, Christopher L. Thomson, Bryon J Hand Surg Glob Online Case Report Malignant melanoma is relatively uncommon and accounts for 1%–3% of all malignant tumors. Malignant melanoma of the hand is exceptionally rare and highly malignant, with rapid progression if left untreated. Early clinical symptoms can be overlooked, and the tumor is often at a late stage when patients seek care, prompting amputation of the affected region. We present a case of a 48-year-old man who presented with a rapidly progressive, large, fungating mass of the distal aspect of the little finger diagnosed as malignant melanoma. We describe the presentation and treatment of this patient, who ultimately underwent partial amputation of the fifth metacarpal. Histologic analysis demonstrated nodular melanoma. Elsevier 2023-02-25 /pmc/articles/PMC10264841/ /pubmed/37323976 http://dx.doi.org/10.1016/j.jhsg.2023.01.015 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Anthony, Taylor Goodman, Aubree Fan, Juston Gnass, Ronaldo D. Sherman, Christopher L. Thomson, Bryon A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand |
title | A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand |
title_full | A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand |
title_fullStr | A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand |
title_full_unstemmed | A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand |
title_short | A Rare Disease Presentation of Malignant Fungating Acral Melanoma of the Hand |
title_sort | rare disease presentation of malignant fungating acral melanoma of the hand |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10264841/ https://www.ncbi.nlm.nih.gov/pubmed/37323976 http://dx.doi.org/10.1016/j.jhsg.2023.01.015 |
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