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Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation

Malignant fibrous histiocytoma (MFH) a pleomorphic sarcoma of uncertain origin was first described by O’Brien and Stout in 1964. It is the most common primary soft tissue sarcoma of late adult life; its occurrence is rare in the pediatric population. MFHs are commonly known to arise in the extremiti...

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Autor principal: Krishnamurthy, Arvind
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204249/
https://www.ncbi.nlm.nih.gov/pubmed/25336806
http://dx.doi.org/10.4103/0971-9261.142015
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author Krishnamurthy, Arvind
author_facet Krishnamurthy, Arvind
author_sort Krishnamurthy, Arvind
collection PubMed
description Malignant fibrous histiocytoma (MFH) a pleomorphic sarcoma of uncertain origin was first described by O’Brien and Stout in 1964. It is the most common primary soft tissue sarcoma of late adult life; its occurrence is rare in the pediatric population. MFHs are commonly known to arise in the extremities and the trunk although it can occur almost anywhere in the body. MFH of the scalp is extremely rare; moreover, there is paucity of literature with regards to prevalence of scalp and skull neoplasms. We present an unusual case of a primary MFH involving the scalp of a 5-year-old child and discuss its unusual clinical presentation, histology with immunohistochemistry correlation and its management. Reviewing the literature of primary MFH of the scalp, our patient to the best of our knowledge, is probably the youngest case reported so far.
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spelling pubmed-42042492014-10-21 Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation Krishnamurthy, Arvind J Indian Assoc Pediatr Surg Case Report Malignant fibrous histiocytoma (MFH) a pleomorphic sarcoma of uncertain origin was first described by O’Brien and Stout in 1964. It is the most common primary soft tissue sarcoma of late adult life; its occurrence is rare in the pediatric population. MFHs are commonly known to arise in the extremities and the trunk although it can occur almost anywhere in the body. MFH of the scalp is extremely rare; moreover, there is paucity of literature with regards to prevalence of scalp and skull neoplasms. We present an unusual case of a primary MFH involving the scalp of a 5-year-old child and discuss its unusual clinical presentation, histology with immunohistochemistry correlation and its management. Reviewing the literature of primary MFH of the scalp, our patient to the best of our knowledge, is probably the youngest case reported so far. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4204249/ /pubmed/25336806 http://dx.doi.org/10.4103/0971-9261.142015 Text en Copyright: © Journal of Indian Association of Pediatric Surgeons http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Krishnamurthy, Arvind
Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation
title Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation
title_full Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation
title_fullStr Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation
title_full_unstemmed Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation
title_short Malignant fibrous histiocytoma of the scalp: A rare differential with a dramatic clinical presentation
title_sort malignant fibrous histiocytoma of the scalp: a rare differential with a dramatic clinical presentation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4204249/
https://www.ncbi.nlm.nih.gov/pubmed/25336806
http://dx.doi.org/10.4103/0971-9261.142015
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