Inflammatory myofibroblastic tumor of the urinary bladder: A systematic review of the literature and report of a case.

IF 1.3 Q3 UROLOGY & NEPHROLOGY Indian Journal of Urology Pub Date : 2024-04-01 DOI:10.4103/iju.iju_50_24
Lory Hage, Michael A O'Donnell, Mohamad Abou Chakra, Amel Kime, Mathilde Sibony, Michaël Peyromaure, Igor Duquesne
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引用次数: 0

Abstract

Introduction: Inflammatory myofibroblastic tumors (IMTs) are intermediate-grade lesions that frequently recur and rarely metastasize. There are currently no guidelines on the management of bladder IMTs. This systematic review aims to describe the clinical presentation and compare the management options for bladder IMTs.

Methods: A PubMed/Medline search was conducted, according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, using the following Mesh terms: ("inflammatory myofibroblastic") AND ("tumor") OR ("tumor") AND ("bladder") AND ("case report"). A total of 75 case reports were included in the analysis.

Results: The mean age of the patients was 36 years. 65% of the cases initially presented with hematuria. 68% of the tumors stained positive for anaplastic lymphoma kinase, and 20% invaded the muscularis. Patients underwent either transurethral resection of the bladder tumor (TURBT) only (34%), TURBT followed by complementary partial cystectomy (16%), or TURBT followed by radical cystectomy (4%). 36% and 9% of the cases underwent partial and radical cystectomy after the initial diagnosis, respectively. Cystectomies were performed using an open (74%), laparoscopic (14%), robotic-assisted (10%), or unknown (2%) approach. At a mean follow-up of 14 months, the recurrence and metastasis rates were about 9% and 4%, respectively. In addition, we present the case of a 49-year-old woman with a bladder IMT who underwent TURBT followed by laparoscopic partial cystectomy. The patient remains tumor free postoperatively (follow-up period of 12 months).

Conclusion: A complete surgical excision of the bladder IMT is crucial for the optimal management of these cases. Proper differentiation of this tumor from sarcoma or leiomyosarcoma leads to the best outcomes.

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膀胱炎性肌成纤维细胞瘤:文献系统回顾与病例报告。
导言炎性肌纤维母细胞瘤(IMTs)是一种中级病变,经常复发,很少转移。目前还没有关于膀胱肌纤维母细胞瘤治疗的指南。本系统性综述旨在描述膀胱IMTs的临床表现并比较其治疗方案:方法:根据《系统综述和元分析首选报告项目》指南,使用以下Mesh术语进行PubMed/Medline检索:("炎性肌纤维母细胞")和("肿瘤")或("肿瘤")和("膀胱")和("病例报告")。共有 75 份病例报告被纳入分析:结果:患者的平均年龄为 36 岁。65%的病例最初表现为血尿。68%的肿瘤无细胞淋巴瘤激酶染色呈阳性,20%的肿瘤侵犯肌肉。患者只接受了经尿道膀胱肿瘤切除术(TURBT)(34%),经尿道膀胱肿瘤切除术后进行了补充性部分膀胱切除术(16%),或经尿道膀胱肿瘤切除术后进行了根治性膀胱切除术(4%)。36%和9%的病例在初步诊断后分别接受了部分和根治性膀胱切除术。膀胱切除术采用开腹(74%)、腹腔镜(14%)、机器人辅助(10%)或未知(2%)方式。在平均 14 个月的随访中,复发率和转移率分别约为 9% 和 4%。此外,我们还介绍了一例 49 岁女性膀胱内肿瘤患者的病例,她接受了 TURBT 术,随后接受了腹腔镜膀胱部分切除术。该患者术后仍无肿瘤(随访 12 个月):结论:彻底切除膀胱IMT对于此类病例的最佳治疗至关重要。结论:膀胱IMT的完整手术切除对于此类病例的最佳治疗至关重要,正确区分该肿瘤与肉瘤或肌层肉瘤可获得最佳疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Indian Journal of Urology
Indian Journal of Urology UROLOGY & NEPHROLOGY-
CiteScore
1.90
自引率
0.00%
发文量
62
审稿时长
33 weeks
期刊介绍: Indian Journal of Urology-IJU (ISSN 0970-1591) is official publication of the Urological Society of India. The journal is published Quarterly. Bibliographic listings: The journal is indexed with Abstracts on Hygiene and Communicable Diseases, CAB Abstracts, Caspur, DOAJ, EBSCO Publishing’s Electronic Databases, Excerpta Medica / EMBASE, Expanded Academic ASAP, Genamics JournalSeek, Global Health, Google Scholar, Health & Wellness Research Center, Health Reference Center Academic, Hinari, Index Copernicus, IndMed, OpenJGate, PubMed, Pubmed Central, Scimago Journal Ranking, SCOLOAR, SCOPUS, SIIC databases, SNEMB, Tropical Diseases Bulletin, Ulrich’s International Periodical Directory
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