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硬膜下血肿的肿瘤样表现:原发性硬脑膜下淋巴瘤的诊断和治疗策略的病例报告和综述。

Tumoral Mimics of Subdural Hematomas: Case Report and Review of Diagnostic and Management Strategies in Primary B-Cell Lymphoma of the Subdural Space.

机构信息

Department of Neurological Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Department of Neurological Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

出版信息

World Neurosurg. 2020 Jan;133:49-54. doi: 10.1016/j.wneu.2019.09.091. Epub 2019 Sep 25.

Abstract

BACKGROUND

Subdural lymphomas are a rare subtype of primary central nervous system lymphomas that can radiographically mimic epidural blood and pose a diagnostic challenge. They can complicate treatment if not preemptively identified.

METHODS

We present a case report of a subdural lymphoma that mimicked a compressive subdural hematoma, and we review the PubMed database for similar cases.

RESULTS

A 77-year-old woman presented with a transient left facial droop and what appeared to be a subdural hematoma on computed tomography scan. The patient underwent surgery, during which grossly abnormal solid epicortical adherent tissue was noted instead of the expected appearance of a subdural hematoma. An intraoperative biopsy was suggestive of lymphoma, and the surgery was converted to a craniectomy. Pathology confirmed the diagnosis of extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue. The patient underwent radiotherapy with no complications or recurrence. Magnetic resonance imaging demonstrated complete resolution of the mass at 3 months after treatment, at which time the patient underwent a synthetic cranioplasty. Seven case reports of primary dural lymphomas mimicking subdural blood were found, with variable pathologic subclassifications.

CONCLUSIONS

Although rare, a primary dural lymphoma can be mistaken for a subdural hematoma on computed tomography scan. The most common subtype is low-grade extranodal marginal zone lymphomas. It is important to keep these diseases in the differential diagnosis, especially when there is incongruence between imaging and the clinical picture, as earlier detection correlates to a stronger therapeutic response.

摘要

背景

硬膜下淋巴瘤是一种罕见的原发性中枢神经系统淋巴瘤亚型,其影像学表现可类似于硬膜外血肿,从而导致诊断困难。如果不能预先识别,它们可能会使治疗复杂化。

方法

我们报告了一例硬膜下淋巴瘤病例,该病例影像学上类似于压迫性硬膜下血肿,并在 PubMed 数据库中检索了类似病例。

结果

一名 77 岁女性因一过性左侧面部下垂和计算机断层扫描(CT)上似乎出现硬膜下血肿而就诊。患者接受了手术,术中发现明显异常的皮质外附壁实性组织,而不是预期的硬膜下血肿外观。术中活检提示为淋巴瘤,手术改为开颅术。病理证实为结外黏膜相关淋巴组织边缘区淋巴瘤。患者接受了放疗,无并发症或复发。磁共振成像(MRI)显示治疗后 3 个月肿块完全消退,此时患者接受了颅骨修补术。共发现 7 例原发性硬脑膜淋巴瘤病例,影像学上类似于硬膜下血肿,其病理亚型各不相同。

结论

尽管罕见,但原发性硬脑膜淋巴瘤在 CT 扫描上可能被误诊为硬膜下血肿。最常见的亚型是低级别的结外黏膜相关淋巴组织边缘区淋巴瘤。在鉴别诊断中应考虑到这些疾病,特别是在影像学与临床表现不一致时,因为早期发现与更强的治疗反应相关。

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