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Metachronous Malignant Fibrous HistiocytomaA Rare Case Report

Malignant fibrous histiocytoma (MFH) is one of the most common types of soft tissue sarcomas in adults. Distant metastases are developed in 30–40% of patients with MFH, with the most common site being the lung. However, metachronous MFH has not been reported previously in literature. This report des...

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Autores principales: Rawal, Gireesha, Zaheer, Sufian, Yadav, Amit Kumar, Dhawan, Indrani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Pathology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358554/
https://www.ncbi.nlm.nih.gov/pubmed/30774689
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author Rawal, Gireesha
Zaheer, Sufian
Yadav, Amit Kumar
Dhawan, Indrani
author_facet Rawal, Gireesha
Zaheer, Sufian
Yadav, Amit Kumar
Dhawan, Indrani
author_sort Rawal, Gireesha
collection PubMed
description Malignant fibrous histiocytoma (MFH) is one of the most common types of soft tissue sarcomas in adults. Distant metastases are developed in 30–40% of patients with MFH, with the most common site being the lung. However, metachronous MFH has not been reported previously in literature. This report describes a case of a 30-year-old man, who had two metachronous thigh tumors, both of which were confirmed to be MFH on histopathology and immunohistochemistry evaluations. A contemporary multidisciplinary approach to therapy including surgery, radiation and chemotherapy was advocated. Two primary sites of MFH raised the possibility of a genetic abnormality that could predispose such a patient to develop multiple primary sites of the same tumor.
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spelling pubmed-63585542019-02-15 Metachronous Malignant Fibrous HistiocytomaA Rare Case Report Rawal, Gireesha Zaheer, Sufian Yadav, Amit Kumar Dhawan, Indrani Iran J Pathol Case Report Malignant fibrous histiocytoma (MFH) is one of the most common types of soft tissue sarcomas in adults. Distant metastases are developed in 30–40% of patients with MFH, with the most common site being the lung. However, metachronous MFH has not been reported previously in literature. This report describes a case of a 30-year-old man, who had two metachronous thigh tumors, both of which were confirmed to be MFH on histopathology and immunohistochemistry evaluations. A contemporary multidisciplinary approach to therapy including surgery, radiation and chemotherapy was advocated. Two primary sites of MFH raised the possibility of a genetic abnormality that could predispose such a patient to develop multiple primary sites of the same tumor. Iranian Society of Pathology 2018 2018-09-25 /pmc/articles/PMC6358554/ /pubmed/30774689 Text en © 2018, IRANIAN JOURNAL OF PATHOLOGY This is an open-access article distributed under the terms of the Creative Commons Attribution-noncommercial 4.0 International License, (https://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Case Report
Rawal, Gireesha
Zaheer, Sufian
Yadav, Amit Kumar
Dhawan, Indrani
Metachronous Malignant Fibrous HistiocytomaA Rare Case Report
title Metachronous Malignant Fibrous HistiocytomaA Rare Case Report
title_full Metachronous Malignant Fibrous HistiocytomaA Rare Case Report
title_fullStr Metachronous Malignant Fibrous HistiocytomaA Rare Case Report
title_full_unstemmed Metachronous Malignant Fibrous HistiocytomaA Rare Case Report
title_short Metachronous Malignant Fibrous HistiocytomaA Rare Case Report
title_sort metachronous malignant fibrous histiocytomaa rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358554/
https://www.ncbi.nlm.nih.gov/pubmed/30774689
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AT zaheersufian metachronousmalignantfibroushistiocytomaararecasereport
AT yadavamitkumar metachronousmalignantfibroushistiocytomaararecasereport
AT dhawanindrani metachronousmalignantfibroushistiocytomaararecasereport