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Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review
RATIONALE: Inflammatory myofibroblastic tumor (IMT) is a rare intermediate soft tissue tumor. Rarely occurring in the urinary bladder, MTs is composed of myofibroblast differentiated spindle cells and accompanied by numerous inflammatory cells, plasma cells and/or Lymphocytes. PATIENT CONCERNS: A 28...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344176/ https://www.ncbi.nlm.nih.gov/pubmed/30608442 http://dx.doi.org/10.1097/MD.0000000000013987 |
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author | Song, Daoqing jiao, Wei Gao, Ze Liu, Ningning Zhang, Shimin Zong, Yuqian Fang, Zhiqing Fan, Yidong |
author_facet | Song, Daoqing jiao, Wei Gao, Ze Liu, Ningning Zhang, Shimin Zong, Yuqian Fang, Zhiqing Fan, Yidong |
author_sort | Song, Daoqing |
collection | PubMed |
description | RATIONALE: Inflammatory myofibroblastic tumor (IMT) is a rare intermediate soft tissue tumor. Rarely occurring in the urinary bladder, MTs is composed of myofibroblast differentiated spindle cells and accompanied by numerous inflammatory cells, plasma cells and/or Lymphocytes. PATIENT CONCERNS: A 28-year-old female, with history of 2 cesarean sections 8 years ago and 2 years ago, was admitted to the emergency department for a 7-day ongoing gross hematuria with clots. DIAGNOSES: A cystoscopy showed a tumor near the bladder neck, computed tomography (CT) showed a mass and massive blood clots in the bladder. Finally, postoperative pathological examination confirmed a diagnosis of inflammatory myofibroblastic tumor of bladder. INTERVENTIONS: The patient was given rehydration and blood transfusion to improve the general condition. Then, emergency transurethral resection of the bladder tumor was performed. OUTCOMES: No metastases to lymph nodes and other organs were found, and no tumor progression was revealed during 3-months of follow-up. LESSONS: IMTs rarely occur in the urinary bladder. Due to the lack of specificity in clinical symptoms, it's difficult to arrive at a definite diagnosis before operation. Therefore, usually, the final diagnosis depends on histomorphological features and the immunohistochemical profile. Further case studies are required to study the biological behavior of this condition. |
format | Online Article Text |
id | pubmed-6344176 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-63441762019-02-04 Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review Song, Daoqing jiao, Wei Gao, Ze Liu, Ningning Zhang, Shimin Zong, Yuqian Fang, Zhiqing Fan, Yidong Medicine (Baltimore) Research Article RATIONALE: Inflammatory myofibroblastic tumor (IMT) is a rare intermediate soft tissue tumor. Rarely occurring in the urinary bladder, MTs is composed of myofibroblast differentiated spindle cells and accompanied by numerous inflammatory cells, plasma cells and/or Lymphocytes. PATIENT CONCERNS: A 28-year-old female, with history of 2 cesarean sections 8 years ago and 2 years ago, was admitted to the emergency department for a 7-day ongoing gross hematuria with clots. DIAGNOSES: A cystoscopy showed a tumor near the bladder neck, computed tomography (CT) showed a mass and massive blood clots in the bladder. Finally, postoperative pathological examination confirmed a diagnosis of inflammatory myofibroblastic tumor of bladder. INTERVENTIONS: The patient was given rehydration and blood transfusion to improve the general condition. Then, emergency transurethral resection of the bladder tumor was performed. OUTCOMES: No metastases to lymph nodes and other organs were found, and no tumor progression was revealed during 3-months of follow-up. LESSONS: IMTs rarely occur in the urinary bladder. Due to the lack of specificity in clinical symptoms, it's difficult to arrive at a definite diagnosis before operation. Therefore, usually, the final diagnosis depends on histomorphological features and the immunohistochemical profile. Further case studies are required to study the biological behavior of this condition. Wolters Kluwer Health 2019-01-04 /pmc/articles/PMC6344176/ /pubmed/30608442 http://dx.doi.org/10.1097/MD.0000000000013987 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Research Article Song, Daoqing jiao, Wei Gao, Ze Liu, Ningning Zhang, Shimin Zong, Yuqian Fang, Zhiqing Fan, Yidong Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review |
title | Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review |
title_full | Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review |
title_fullStr | Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review |
title_full_unstemmed | Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review |
title_short | Inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: A Case report and literature review |
title_sort | inflammatory myofibroblastic tumor of urinary bladder with severe hematuria: a case report and literature review |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344176/ https://www.ncbi.nlm.nih.gov/pubmed/30608442 http://dx.doi.org/10.1097/MD.0000000000013987 |
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