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Merkel cell carcinoma in the community setting: a case report

Merkel cell carcinoma (MCC) is a rare neuroendocrine tumor of the skin initially believed to arise from the Merkel cells. In the community setting a general radiation oncologist may only encounter this pathology in a handful of cases over the course of their career. Due to the low incidence of this...

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Detalles Bibliográficos
Autores principales: Callaghan, Cameron M., Amornmarn, Rumpa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Radiation Oncology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074072/
https://www.ncbi.nlm.nih.gov/pubmed/29627970
http://dx.doi.org/10.3857/roj.2017.00479
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author Callaghan, Cameron M.
Amornmarn, Rumpa
author_facet Callaghan, Cameron M.
Amornmarn, Rumpa
author_sort Callaghan, Cameron M.
collection PubMed
description Merkel cell carcinoma (MCC) is a rare neuroendocrine tumor of the skin initially believed to arise from the Merkel cells. In the community setting a general radiation oncologist may only encounter this pathology in a handful of cases over the course of their career. Due to the low incidence of this malignancy, few prospective randomized controlled trials have ever been conducted and therefore guidelines are based on relatively lower levels of evidence upon which the clinical recommendations are made. We discuss the case of a female in her 90s presenting with a classic MCC primary lesion, as well as satellite lesions proximal to both the primary and the draining regional lymph nodes with no evidence of nodal involvement. Here we discuss the presentation, management, treatment planning, underlying pathology, results and sequelae of treatment. We also review new treatment modalities, and the most current staging systems and guidelines.
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spelling pubmed-60740722018-08-23 Merkel cell carcinoma in the community setting: a case report Callaghan, Cameron M. Amornmarn, Rumpa Radiat Oncol J Case Report Merkel cell carcinoma (MCC) is a rare neuroendocrine tumor of the skin initially believed to arise from the Merkel cells. In the community setting a general radiation oncologist may only encounter this pathology in a handful of cases over the course of their career. Due to the low incidence of this malignancy, few prospective randomized controlled trials have ever been conducted and therefore guidelines are based on relatively lower levels of evidence upon which the clinical recommendations are made. We discuss the case of a female in her 90s presenting with a classic MCC primary lesion, as well as satellite lesions proximal to both the primary and the draining regional lymph nodes with no evidence of nodal involvement. Here we discuss the presentation, management, treatment planning, underlying pathology, results and sequelae of treatment. We also review new treatment modalities, and the most current staging systems and guidelines. The Korean Society for Radiation Oncology 2018-06 2018-04-12 /pmc/articles/PMC6074072/ /pubmed/29627970 http://dx.doi.org/10.3857/roj.2017.00479 Text en Copyright © 2018 The Korean Society for Radiation Oncology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (http://creativecommons.org/licenses/by-nc/4.0) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Callaghan, Cameron M.
Amornmarn, Rumpa
Merkel cell carcinoma in the community setting: a case report
title Merkel cell carcinoma in the community setting: a case report
title_full Merkel cell carcinoma in the community setting: a case report
title_fullStr Merkel cell carcinoma in the community setting: a case report
title_full_unstemmed Merkel cell carcinoma in the community setting: a case report
title_short Merkel cell carcinoma in the community setting: a case report
title_sort merkel cell carcinoma in the community setting: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074072/
https://www.ncbi.nlm.nih.gov/pubmed/29627970
http://dx.doi.org/10.3857/roj.2017.00479
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