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本文引用的文献

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Intra-abdominal multicentric inflammatory myofibroblastic tumors mimicking ruptured appendicitis.酷似破裂性阑尾炎的腹腔内多中心炎性肌纤维母细胞瘤
Int J Surg Case Rep. 2022 Apr;93:106990. doi: 10.1016/j.ijscr.2022.106990. Epub 2022 Mar 29.
2
Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity.阑尾炎性肌成纤维细胞瘤:一种罕见的临床实体。
Int J Surg Case Rep. 2021 Dec;89:106607. doi: 10.1016/j.ijscr.2021.106607. Epub 2021 Nov 22.
3
[Clinicopathological features of inflammatory myofibroblastic tumor].[炎性肌纤维母细胞瘤的临床病理特征]
Zhonghua Bing Li Xue Za Zhi. 2021 Mar 8;50(3):194-200. doi: 10.3760/cma.j.cn112151-20200806-00627.
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The SCARE 2020 Guideline: Updating Consensus Surgical CAse REport (SCARE) Guidelines.SCARE 2020 指南:更新共识手术病例报告(SCARE)指南。
Int J Surg. 2020 Dec;84:226-230. doi: 10.1016/j.ijsu.2020.10.034. Epub 2020 Nov 9.
5
An Inflammatory Myofibroblastic Tumor of the Appendix Mimicking an Appendicular Malignant Lesion.一例酷似阑尾恶性病变的阑尾炎性肌纤维母细胞瘤
Clin Pathol. 2020 Feb 18;13:2632010X20905843. doi: 10.1177/2632010X20905843. eCollection 2020 Jan-Dec.
6
Inflammatory Myofibroblastic Tumors: Current Update.炎性肌纤维母细胞瘤:最新进展
Radiol Clin North Am. 2016 May;54(3):553-63. doi: 10.1016/j.rcl.2015.12.005. Epub 2016 Mar 12.
7
Inflammatory myofibroblastic tumor of the appendix arising after treatment of gastric cancer: a case report and review of the literature.阑尾炎性肌纤维母细胞瘤继发于胃癌治疗后:病例报告及文献复习。
APMIS. 2014 Jul;122(7):657-9. doi: 10.1111/apm.12205. Epub 2013 Dec 5.
8
Abdominal inflammatory myofibroblastic tumor: report on four cases and review of literature.腹部炎性肌纤维母细胞瘤:4例报告并文献复习
Iran J Pediatr. 2011 Dec;21(4):543-8.
9
Inflammatory myofibroblastic tumor appendix with concomitant mucosal dysplasia, simulating pseudomyxoma on preoperative aspiration cytology.阑尾炎性肌纤维母细胞瘤伴黏膜发育异常,术前细针穿刺细胞学检查模拟黏液性囊腺瘤。
J Cancer Res Ther. 2012 Apr-Jun;8(2):317-9. doi: 10.4103/0973-1482.99004.
10
Inflammatory pseudo-tumour of the appendix and acute appendicitis: a case report.阑尾炎性假瘤与急性阑尾炎:一例报告
Acta Chir Belg. 2008 Jul-Aug;108(4):451-3. doi: 10.1080/00015458.2008.11680261.

一例表现为急性阑尾炎的阑尾炎性肌纤维母细胞瘤罕见病例:病例报告

A rare case of an inflammatory myofibroblastic tumor of the appendix presenting as acute appendicitis: A case report.

作者信息

Khadka Manoj, Basukala Sunil, Khadka Manita, Kc Manoj, Karki Gaurav, Gurung Amol

机构信息

Shree Birendra Hospital, Chhauni, Kathmandu, Nepal.

Department of Surgery, Shree Birendra Hospital, Chhauni, Kathmandu, Nepal.

出版信息

Int J Surg Case Rep. 2023 Apr;105:108076. doi: 10.1016/j.ijscr.2023.108076. Epub 2023 Mar 27.

DOI:10.1016/j.ijscr.2023.108076
PMID:37018945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10112167/
Abstract

INTRODUCTION AND IMPORTANCE

An inflammatory myofibroblastic tumor is commonly seen in the lungs but rarely in the appendix. It has a distinct inflammatory cell component and myofibroblastic component. The study presents an inflammatory myofibroblastic tumor of the appendix in an elderly who presented with acute appendicitis and was later found to have an appendicular mass intraoperatively.

CASE PRESENTATION

Herein, we report a case of inflammatory myofibroblastic tumor of the appendix in a 59 years old female who presented with acute abdomen, features suggestive of acute appendicitis clinically. However, the intra-operative findings showed an appendicular mass involving the base of the appendix for which a right hemicolectomy was done. The histopathological examination of the resected specimen later confirmed it as an inflammatory myofibroblastic tumor of the appendix.

CLINICAL DISCUSSION

An inflammatory myofibroblastic tumor is common in the lungs, whereas rare in the appendix. It primarily involves children and young adults. It can present as mimic appendicitis or appendicular mass and should thus be considered in the differentials of these.

CONCLUSION

The rare presentation of inflammatory myofibroblastic tumor of the appendix makes it likely to be missed resulting in overzealous resection of the tumor. Thus, it is important to consider it in the differential diagnosis of acute appendicitis and manage it accordingly.

摘要

引言与重要性

炎性肌纤维母细胞瘤常见于肺部,但罕见于阑尾。它具有独特的炎症细胞成分和肌纤维母细胞成分。本研究报告了一例发生于老年患者的阑尾炎性肌纤维母细胞瘤,该患者最初表现为急性阑尾炎,术中发现阑尾肿物。

病例介绍

在此,我们报告一例59岁女性阑尾炎性肌纤维母细胞瘤病例,该患者以急腹症就诊,临床特征提示急性阑尾炎。然而,术中发现阑尾肿物累及阑尾根部,遂行右半结肠切除术。切除标本的组织病理学检查后来证实为阑尾炎性肌纤维母细胞瘤。

临床讨论

炎性肌纤维母细胞瘤常见于肺部,而在阑尾中罕见。它主要累及儿童和年轻人。它可表现为类似阑尾炎或阑尾肿物,因此在这些疾病的鉴别诊断中应予以考虑。

结论

阑尾炎性肌纤维母细胞瘤的罕见表现可能导致漏诊,从而导致对肿瘤的过度切除。因此,在急性阑尾炎的鉴别诊断中考虑到它并进行相应处理很重要。