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Case Reports
. 2024 Mar 29:15:113.
doi: 10.25259/SNI_792_2023. eCollection 2024.

Primary extranodal marginal zone mucosa-associated lymphoid tissue-type B-cell lymphoma involving the dura: A case report

Affiliations
Case Reports

Primary extranodal marginal zone mucosa-associated lymphoid tissue-type B-cell lymphoma involving the dura: A case report

Ryo Hamamoto et al. Surg Neurol Int. .

Abstract

Background: Primary extranodal marginal zone mucosa-associated lymphoid tissue-type B-cell lymphoma (EMZMBCL), which presents as a dural mass, is a rare intracranial tumor that mimics a subdural hematoma or meningioma.

Case description: A 49-year-old woman presented to our hospital with transient right upper limb paresis, dysarthria for 10 min, and ongoing right upper-limb numbness. Computed tomography (CT) of the head revealed extra-axial lesions in the left frontal and parietal lobes. Based on the initial CT findings in the emergency room, an acute subdural hematoma was suspected. However, meningiomas and other intracranial tumors were also listed as differential diagnoses because there was no history of head trauma or coagulation abnormalities on blood examination, and further imaging studies were performed. Imaging findings suggested a subdural neoplastic lesion. A partial resection was performed for the lesion. Based on histopathological and immunohistochemical examinations, the patient was diagnosed with EMZMBCL. Whole-brain and intensity-modulated radiation therapies were administered as adjuvant therapies. The patient was discharged without neurological deficits.

Conclusion: EMZMBCL is a rare disease that should be considered in the differential diagnosis of subdural lesions, especially when there is no history of trauma or abnormalities in the coagulation system. The patient had a favorable outcome after selecting radiotherapy as the adjuvant therapy.

Keywords: Intracranial tumor; Meningioma; Primary extranodal marginal zone mucosa-associated lymphoid tissue-type B-cell lymphoma; Radiotherapy; Subdural hematoma.

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Figures

Figure 1:
Figure 1:
Axial (a) and coronal (b) computed tomography (CT) without contrast demonstrates a high-density subdural lesion. Axial (c) and coronal (d) magnetic resonance imaging with gadolinium contrast show residual contrast-enhancing extra-axial masses in the left frontal, temporal, and parietal lesions. Anteroposterior (e) and lateral (f) view of the left external carotid artery angiogram indicate arterial phase blush within the left convexity lesion. (g and h) Intraoperative findings showed a thickened dura mater (arrows) and a large tumor.
Figure 2:
Figure 2:
Histopathological and Immunohistochemical features of EMZMBCL. (a) Small lymphocytic infiltration (hematoxylin and eosin). (b) CD20 and (c) Insulin-like growth factor 2 mRNA-binding protein-3 (IMP3) immunohistochemical stains show diffuse positive. Immunohistochemical examination revealed immunoglobulin light-chain restriction (Kappa (d): Lambda (e) = 100:2). EMZMBCL: Extranodal marginal zone mucosa-associated lymphoid tissue-type B-cell lymphoma.
Figure 3:
Figure 3:
Preradiotherapy magnetic resonance imaging (MRI). Axial (a) and coronal (b) MRI with gadolinium contrast show residual contrast-enhancing extra-axial masses in the left frontal, temporal, and parietal lesions. The thickening and enhancement of the dura extend along the falx and the left frontal and parietal lobes. MRI at three months after radiation therapy. Axial (c) and coronal (d) MRI with gadolinium contrast indicate the disappearance of residual contrast-enhancing extra-axial masses in the left frontal, temporal, and parietal lesions and normalization of the dural thickening and enhancement. MRI at eight months after radiation therapy. Axial (e) and coronal (f) MRI with gadolinium contrast reveal no recurrence.

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