Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report

Primary malignant fibrous histiocytoma of the renal pelvis is extremely rare. This article reports a pathologically confirmed case. Surgery is the main treatment for this disease. Chemotherapy and radiotherapy have been reported to be ineffective. It is difficult to differentiate it from urothelial...

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Detalles Bibliográficos
Autores principales: Chen, YueBing, Rao, Dapang, Zhu, Haibo, Yu, Haifeng, Yang, ShiKun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869917/
https://www.ncbi.nlm.nih.gov/pubmed/24368887
http://dx.doi.org/10.2147/OTT.S45048
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author Chen, YueBing
Rao, Dapang
Zhu, Haibo
Yu, Haifeng
Yang, ShiKun
author_facet Chen, YueBing
Rao, Dapang
Zhu, Haibo
Yu, Haifeng
Yang, ShiKun
author_sort Chen, YueBing
collection PubMed
description Primary malignant fibrous histiocytoma of the renal pelvis is extremely rare. This article reports a pathologically confirmed case. Surgery is the main treatment for this disease. Chemotherapy and radiotherapy have been reported to be ineffective. It is difficult to differentiate it from urothelial tumor of the renal pelvis and renal cell carcinoma by preoperative laboratory and radiological evaluation. Immunohistochemical study is helpful in confirming the diagnosis of the disease. This report discusses the clinical manifestations, pathohistological characteristics, treatment, and prognosis of the case reported.
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spelling pubmed-38699172013-12-24 Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report Chen, YueBing Rao, Dapang Zhu, Haibo Yu, Haifeng Yang, ShiKun Onco Targets Ther Case Report Primary malignant fibrous histiocytoma of the renal pelvis is extremely rare. This article reports a pathologically confirmed case. Surgery is the main treatment for this disease. Chemotherapy and radiotherapy have been reported to be ineffective. It is difficult to differentiate it from urothelial tumor of the renal pelvis and renal cell carcinoma by preoperative laboratory and radiological evaluation. Immunohistochemical study is helpful in confirming the diagnosis of the disease. This report discusses the clinical manifestations, pathohistological characteristics, treatment, and prognosis of the case reported. Dove Medical Press 2013-12-17 /pmc/articles/PMC3869917/ /pubmed/24368887 http://dx.doi.org/10.2147/OTT.S45048 Text en © 2014 Chen et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Case Report
Chen, YueBing
Rao, Dapang
Zhu, Haibo
Yu, Haifeng
Yang, ShiKun
Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report
title Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report
title_full Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report
title_fullStr Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report
title_full_unstemmed Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report
title_short Primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report
title_sort primary malignant fibrous histiocytoma of the renal pelvis: a 78-month follow-up case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869917/
https://www.ncbi.nlm.nih.gov/pubmed/24368887
http://dx.doi.org/10.2147/OTT.S45048
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