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病例报告:原发性颅内黏膜相关淋巴组织淋巴瘤,表现为分别累及海绵窦和轴外硬脑膜的两个原发性肿瘤。

Case report: Primary intracranial mucosa-associated lymphoid tissue lymphoma presenting as two primary tumors involving the cavernous sinus and extra-axial dura, respectively.

作者信息

Tian Shiyun, Pan Tao, Gao Bingbing, Li Wanyao, Liu Jiashen, Zou Kun, Miao Yanwei

机构信息

Department of Radiology, First Affiliated Hospital of Dalian Medical University, Dalian, China.

The Interventional Therapy Department, First Affiliated Hospital, Dalian Medical University, Dalian, China.

出版信息

Front Oncol. 2023 Jan 4;12:927086. doi: 10.3389/fonc.2022.927086. eCollection 2022.

Abstract

Primary intracranial mucosa-associated lymphoid tissue (MALT) lymphoma is a rare type of brain tumor, with only a few reported cases worldwide that mostly have only one lesion with conventional magnetic resonance imaging (MRI) findings. Here, we present a special case of intracranial MALT lymphoma with two mass lesions radiographically consistent with meningiomas on MRI before the operation. A 66-year-old woman was admitted to the hospital with intermittent right facial pain for 1 year, aggravated for the last month. Brain MRI showed two extracerebral solid masses with similar MR signal intensity. One mass was crescent-shaped beneath the skull, and the other was in the cavernous sinus area. Lesions showed isointensity on T1WI and T2WI and an intense homogeneous enhancement after contrast agent injection. Both lesions showed hyperintensity in amide proton transfer-weighted images. The two masses were all surgically resected. The postoperative pathology indicated extranodal marginal zone B-cell lymphoma of MALT. To improve awareness of intracranial MALT lymphoma in the differential diagnosis of extra-axial lesions among clinicians, we present this report and briefly summarize previously reported cases to describe the clinical, pathological, radiological, and treatment features.

摘要

原发性颅内黏膜相关淋巴组织(MALT)淋巴瘤是一种罕见的脑肿瘤,全球仅有少数病例报道,大多数病例在传统磁共振成像(MRI)检查中仅表现为单个病灶。在此,我们报告一例特殊的颅内MALT淋巴瘤病例,术前MRI显示两个肿块性病变,影像学表现与脑膜瘤一致。一名66岁女性因间歇性右面部疼痛1年入院,近1个月加重。脑部MRI显示两个脑外实性肿块,具有相似的MR信号强度。一个肿块位于颅骨下方呈新月形,另一个位于海绵窦区。病变在T1WI和T2WI上呈等信号,注射对比剂后呈均匀强化。两个病变在酰胺质子转移加权图像上均呈高信号。两个肿块均行手术切除。术后病理显示为MALT型结外边缘区B细胞淋巴瘤。为提高临床医生对颅内MALT淋巴瘤在轴外病变鉴别诊断中的认识,我们报告本病例并简要总结既往报道的病例,以描述其临床、病理、影像学和治疗特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f876/9846770/0fcd83846d7f/fonc-12-927086-g001.jpg

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