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脾脏炎性假瘤样滤泡树突状细胞肉瘤的影像学与病理学对比:一例报告及文献复习

Imaging and pathological comparison of inflammatory pseudotumor-like follicular dendritic cell sarcoma of the spleen: A case report and literature review.

作者信息

Chen Fuxing, Li Junqiang, Xie Pingkun

机构信息

Department of Radiology, Beilun District People's Hospital, Ningbo, China.

Department of Pathology, Beilun District People's Hospital, Ningbo, China.

出版信息

Front Surg. 2022 Sep 5;9:973106. doi: 10.3389/fsurg.2022.973106. eCollection 2022.

Abstract

BACKGROUND

Inflammatory pseudotumor-like follicular dendritic cell sarcoma (IPT-like FDCS) is a rare subtype of follicular dendritic cell sarcoma (FDCS) that is mainly located in the liver and spleen (1). Splenic IPT-like FDCS is a rare low-grade malignancy with non-specific clinical manifestations and laboratory findings. Herein, we reported the pathological and imaging features of a case with splenic IPT-like FDCS.

CASE PRESENTATION

A 57-year-old woman was found to have a mass in the spleen during a physical examination and was hospitalized for further treatment. Her laboratory results were within the normal range. Unenhanced and contrast-enhanced computed tomography scans of the whole abdomen showed a round mass in the spleen, with a diameter of about 5 cm. After further examination with enhanced MRI, a provisional diagnosis of splenic hemangioma or splenic hamartoma was made. The patient underwent splenectomy, and the pathological diagnosis was splenic IPT-like FDCS. No tumor recurrence or metastasis was found during the 1-year follow-up after the operation.

CONCLUSIONS

Herein, we reported a case of splenic IPT-like FDCS. Although the clinical examination and laboratory examination lack specificity, the imaging of this case showed that the lesion was a solid mass with progressive enhancement, and the central scar showed the characteristics of delayed enhancement, which facilitated the diagnosis.

摘要

背景

炎性假瘤样滤泡树突状细胞肉瘤(IPT样FDCS)是滤泡树突状细胞肉瘤(FDCS)的一种罕见亚型,主要位于肝脏和脾脏(1)。脾脏IPT样FDCS是一种罕见的低级别恶性肿瘤,临床表现和实验室检查结果均无特异性。在此,我们报告一例脾脏IPT样FDCS的病理及影像学特征。

病例介绍

一名57岁女性在体检时发现脾脏有肿物,遂住院进一步治疗。其实验室检查结果均在正常范围内。全腹平扫及增强CT扫描显示脾脏有一圆形肿物,直径约5 cm。经增强MRI进一步检查后,初步诊断为脾脏血管瘤或脾脏错构瘤。患者接受了脾切除术,病理诊断为脾脏IPT样FDCS。术后1年随访未发现肿瘤复发或转移。

结论

在此,我们报告一例脾脏IPT样FDCS。尽管临床检查和实验室检查缺乏特异性,但该病例的影像学表现显示病变为实性肿物,呈渐进性强化,中央瘢痕呈延迟强化特征,有助于诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ec0/9483013/ae072799452e/fsurg-09-973106-g001.jpg

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