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累及上矢状窦前三分之一和中三分之一的双侧矢旁和镰旁脑膜瘤的挑战性切除术:病例报告及文献综述

Challenging Resection of Bilateral Parasagittal and Falcine Meningioma Involving Both Anterior Third and Middle Third of the Superior Sagittal Sinus: A Case Report and Literature Review.

作者信息

Alzughaibi Rawia A, Almuhammadi Ghaidaa A, Alasmari Saud S, Khoja Maamoun M, Almashni Aysam A

机构信息

College of Medicine, Taibah University, Madina, SAU.

College of Medicine, King Khalid University, Abha, SAU.

出版信息

Cureus. 2024 Jul 18;16(7):e64865. doi: 10.7759/cureus.64865. eCollection 2024 Jul.

Abstract

Meningiomas typically manifest as benign, slow-growing, and well-defined tumors on a macroscopic level and are usually asymptomatic. However, the mass effect caused by large meningiomas may lead to various neurological symptoms, commonly headaches and visual problems. Radiological imaging can establish the diagnosis, and a biopsy can provide a definitive diagnosis. Our case report describes the surgical intervention for bilateral parasagittal-falcine meningioma in a 57-year-old male who presented to the emergency department with a tonic-clonic seizure. On examination, he had a bifrontal longitudinal mass. Magnetic resonance imaging (MRI) revealed a large anterior superior falcine extra-axial mass, measuring about 5.7 x 5.3 x 3.1 cm, with surrounding vasogenic edema and superior sagittal sinus invasion. He underwent surgery for tumor resection involving the anterior third and middle third of the superior sagittal sinus without radiotherapy. He did not develop any intraoperative complications, and during the post-operative evaluation, he was symptom-free. A follow-up MRI with contrast performed three months later showed no neurological complications or recurrent tumor. To achieve better outcomes, surgical intervention for parasagittal and falcine meningiomas involving the superior sagittal sinus should aim to eliminate clinical signs, control tumor growth, and prevent neurological deterioration post-operatively.

摘要

脑膜瘤在宏观层面通常表现为良性、生长缓慢且边界清晰的肿瘤,通常无症状。然而,大型脑膜瘤引起的占位效应可能导致各种神经症状,常见的有头痛和视觉问题。放射影像学检查可确立诊断,活检可提供确诊依据。我们的病例报告描述了一名57岁男性双侧矢状窦旁-大脑镰脑膜瘤的手术干预情况,该患者因强直阵挛发作就诊于急诊科。检查时,他有一个双额纵向肿块。磁共振成像(MRI)显示一个位于大脑镰前上方的大型轴外肿块,大小约为5.7×5.3×3.1厘米,伴有周围血管源性水肿和上矢状窦侵犯。他接受了手术切除肿瘤,手术涉及上矢状窦前三分之一和中三分之一,未进行放疗。他未发生任何术中并发症,术后评估时无症状。三个月后进行的增强MRI随访显示无神经并发症或肿瘤复发。为获得更好的治疗效果,涉及上矢状窦的矢状窦旁和大脑镰脑膜瘤的手术干预应旨在消除临床症状、控制肿瘤生长并防止术后神经功能恶化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f7/11330339/9ce5d86036b8/cureus-0016-00000064865-i01.jpg

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