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Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma

Merkel cell carcinoma (MCC) is a rare neuroendocrine malignancy of the skin that is highly aggressive and often metastasizes early. MCC is diagnosed based on histopathological findings and is most commonly treated with surgical resection, which may be accompanied by chemotherapy and/or radiation. Th...

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Autores principales: Cartwright, Jake K., Snyder, Daniel H., Moreno, Francisco G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124612/
https://www.ncbi.nlm.nih.gov/pubmed/35620264
http://dx.doi.org/10.1002/ccr3.5891
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author Cartwright, Jake K.
Snyder, Daniel H.
Moreno, Francisco G.
author_facet Cartwright, Jake K.
Snyder, Daniel H.
Moreno, Francisco G.
author_sort Cartwright, Jake K.
collection PubMed
description Merkel cell carcinoma (MCC) is a rare neuroendocrine malignancy of the skin that is highly aggressive and often metastasizes early. MCC is diagnosed based on histopathological findings and is most commonly treated with surgical resection, which may be accompanied by chemotherapy and/or radiation. This report describes a 55‐year‐old male patient with the history of recurrent malignant melanoma of the right pinna and subsequent excision. Three years following the excision of melanoma, he presented with a lesion to the right forehead as well as a right‐sided neck mass that were found to be metastatic Merkel cell carcinoma.
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spelling pubmed-91246122022-05-25 Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma Cartwright, Jake K. Snyder, Daniel H. Moreno, Francisco G. Clin Case Rep Case Reports Merkel cell carcinoma (MCC) is a rare neuroendocrine malignancy of the skin that is highly aggressive and often metastasizes early. MCC is diagnosed based on histopathological findings and is most commonly treated with surgical resection, which may be accompanied by chemotherapy and/or radiation. This report describes a 55‐year‐old male patient with the history of recurrent malignant melanoma of the right pinna and subsequent excision. Three years following the excision of melanoma, he presented with a lesion to the right forehead as well as a right‐sided neck mass that were found to be metastatic Merkel cell carcinoma. John Wiley and Sons Inc. 2022-05-22 /pmc/articles/PMC9124612/ /pubmed/35620264 http://dx.doi.org/10.1002/ccr3.5891 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Cartwright, Jake K.
Snyder, Daniel H.
Moreno, Francisco G.
Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma
title Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma
title_full Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma
title_fullStr Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma
title_full_unstemmed Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma
title_short Development of metastatic Merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma
title_sort development of metastatic merkel cell carcinoma following the excision of same‐sided recurrent auricular melanoma
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124612/
https://www.ncbi.nlm.nih.gov/pubmed/35620264
http://dx.doi.org/10.1002/ccr3.5891
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