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A unique tripartite collision tumor of the esophagus: A case report
RATIONALE: We report a unique case of a tripartite esophageal collision tumor consisting of three separate histologic types. PATIENTS CONCERNS: Therapeutic dilemmas on the proper treatment of those rare neoplasms remain unanswered considering both proper surgical therapy and adjuvant therapy. DIAGNO...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728851/ https://www.ncbi.nlm.nih.gov/pubmed/29245236 http://dx.doi.org/10.1097/MD.0000000000008784 |
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author | Schizas, Dimitrios Michalinos, Adamantios Alexandrou, Paraskevi Moris, Demetrios Baliou, Evangelia Tsilimigras, Diamantis Throupis, Theodore Liakakos, Theodore |
author_facet | Schizas, Dimitrios Michalinos, Adamantios Alexandrou, Paraskevi Moris, Demetrios Baliou, Evangelia Tsilimigras, Diamantis Throupis, Theodore Liakakos, Theodore |
author_sort | Schizas, Dimitrios |
collection | PubMed |
description | RATIONALE: We report a unique case of a tripartite esophageal collision tumor consisting of three separate histologic types. PATIENTS CONCERNS: Therapeutic dilemmas on the proper treatment of those rare neoplasms remain unanswered considering both proper surgical therapy and adjuvant therapy. DIAGNOSE: In this paper, we report a unique case of a patient with a tripartite esophageal collision tumor consisting of a small cell carcinoma, an adenocarcinoma of medium differentiation and a signet ring cell carcinoma. Diagnosis is difficult as clinical presentation of the patient was undistinguishable from other, commoner tumor types. INTERVENTIONS: The patient's diagnostic and therapeutic course along with available data on the collisions tumor's biological behavior and treatment are briefly discussed. OUTCOMES: Esophagectomy is the best treatment options for these patients. Unique nature of this tumor demands aggresive oncologic treatment. LESSONS: Collision tumors are rare neoplasms consisting of distinct cell populations developing in juxtaposition to one another without any areas of intermingling. Various cell types can be found. However, collision neoplasms of the esophagus combining adenomatous and neuroendocrine components are exceedingly rare, with only 5 cases described to date in the literature. Given their rarity, limited information is available on their tumorigenesis, biological behavior and clinical course. In general, these tumors are aggressive neoplasms and significantly affect patient treatment and prognosis. |
format | Online Article Text |
id | pubmed-5728851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-57288512017-12-20 A unique tripartite collision tumor of the esophagus: A case report Schizas, Dimitrios Michalinos, Adamantios Alexandrou, Paraskevi Moris, Demetrios Baliou, Evangelia Tsilimigras, Diamantis Throupis, Theodore Liakakos, Theodore Medicine (Baltimore) 7100 RATIONALE: We report a unique case of a tripartite esophageal collision tumor consisting of three separate histologic types. PATIENTS CONCERNS: Therapeutic dilemmas on the proper treatment of those rare neoplasms remain unanswered considering both proper surgical therapy and adjuvant therapy. DIAGNOSE: In this paper, we report a unique case of a patient with a tripartite esophageal collision tumor consisting of a small cell carcinoma, an adenocarcinoma of medium differentiation and a signet ring cell carcinoma. Diagnosis is difficult as clinical presentation of the patient was undistinguishable from other, commoner tumor types. INTERVENTIONS: The patient's diagnostic and therapeutic course along with available data on the collisions tumor's biological behavior and treatment are briefly discussed. OUTCOMES: Esophagectomy is the best treatment options for these patients. Unique nature of this tumor demands aggresive oncologic treatment. LESSONS: Collision tumors are rare neoplasms consisting of distinct cell populations developing in juxtaposition to one another without any areas of intermingling. Various cell types can be found. However, collision neoplasms of the esophagus combining adenomatous and neuroendocrine components are exceedingly rare, with only 5 cases described to date in the literature. Given their rarity, limited information is available on their tumorigenesis, biological behavior and clinical course. In general, these tumors are aggressive neoplasms and significantly affect patient treatment and prognosis. Wolters Kluwer Health 2017-12-08 /pmc/articles/PMC5728851/ /pubmed/29245236 http://dx.doi.org/10.1097/MD.0000000000008784 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 7100 Schizas, Dimitrios Michalinos, Adamantios Alexandrou, Paraskevi Moris, Demetrios Baliou, Evangelia Tsilimigras, Diamantis Throupis, Theodore Liakakos, Theodore A unique tripartite collision tumor of the esophagus: A case report |
title | A unique tripartite collision tumor of the esophagus: A case report |
title_full | A unique tripartite collision tumor of the esophagus: A case report |
title_fullStr | A unique tripartite collision tumor of the esophagus: A case report |
title_full_unstemmed | A unique tripartite collision tumor of the esophagus: A case report |
title_short | A unique tripartite collision tumor of the esophagus: A case report |
title_sort | unique tripartite collision tumor of the esophagus: a case report |
topic | 7100 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5728851/ https://www.ncbi.nlm.nih.gov/pubmed/29245236 http://dx.doi.org/10.1097/MD.0000000000008784 |
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