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大网膜炎性肌纤维母细胞瘤的影像学表现:1例报告

Imaging findings of inflammatory myofibroblastic tumor from the greater omentum: One case report.

作者信息

Liang Wenjie, Lin Shengzhang, Chen Zhihua

机构信息

Department of Radiology Department of Hepatobiliary and Pancreatic Surgery, the First Affiliated Hospital, College of Medicine, Zhejiang University.79# Qingchun Road, Hangzhou City, Zhejiang Province Department of General Surgery, the First People's Hospital of Taicang City, Taicang Affiliated Hospital of Soochow University, Taicang, Suzhou, China.

出版信息

Medicine (Baltimore). 2017 Oct;96(41):e8297. doi: 10.1097/MD.0000000000008297.

Abstract

RATIONALE

Inflammatory myofibroblastic tumors (IMTs) are rare neoplastic lesions with benign tendency. Even more rare are IMTs from the greater omentum (GO-IMT). A GO-IMT is easily misdiagnosed as other malignant tumors before operation; thus, clinicians need to be familiar with its imaging findings. Here, we report the imaging findings of a GO-IMT patient presenting with a pelvic mass.

PATIENT CONCERNS

Ultrasound of the IMT in the pelvic cavity showed a hypoechoic mass. A computed tomography (CT) scan showed a nearly circular soft tissue mass with a clear border and heterogeneous density, and the surrounding tissues were pushed and compressed. Contrast-enhanced CT showed severe persistent enhancement in the lesion edges and mural nodules, but not in the central necrosis.

DIAGNOSES

Histopathology and immunohistochemistry confirmed that the mass was a GO-IMT.

INTERVENTIONS

The tumor was resected after preoperative preparation.

OUTCOMES

No recurrence or metastasis was found during a short-term follow-up.

LESSONS

The GO-IMT is an inferior epigastric mass in the periphery of the bowel, and is usually well-demarcated without calcification or lymphadenopathy. Contrast-enhanced CT showed a heterogeneous hypervascular mass where the center necrosis, the edge of the tumor, and the mural nodules can be partially reinforced.

摘要

原理

炎性肌纤维母细胞瘤(IMT)是一种具有良性倾向的罕见肿瘤性病变。来自大网膜的IMT(GO-IMT)更为罕见。GO-IMT在术前很容易被误诊为其他恶性肿瘤;因此,临床医生需要熟悉其影像学表现。在此,我们报告一例表现为盆腔肿块的GO-IMT患者的影像学表现。

患者情况

盆腔内IMT的超声检查显示为低回声肿块。计算机断层扫描(CT)显示一个边界清晰、密度不均匀的近圆形软组织肿块,周围组织被推压和压缩。增强CT显示病变边缘和壁结节有明显的持续强化,但中央坏死区无强化。

诊断

组织病理学和免疫组织化学证实该肿块为GO-IMT。

干预措施

术前准备后切除肿瘤。

结果

短期随访期间未发现复发或转移。

经验教训

GO-IMT是位于肠管周围的下腹部肿块,通常边界清晰,无钙化或淋巴结肿大。增强CT显示为不均匀的高血供肿块,中央坏死,肿瘤边缘和壁结节可部分强化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15d9/5662327/831549bb43ed/medi-96-e8297-g001.jpg

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