Hamilton D Kojo, Bourne T David, Ahmed Hazem, Cousar John B, Mandell James W, Sheehan Jason P
Department of Neurological Surgery, University of Virginia, Charlottesville 22908, USA.
Neurosurgery. 2006 Sep;59(3):E703-4; discussion E703-4. doi: 10.1227/01.NEU.0000229057.50372.06.
We present an unusual dural-based follicular lymphoma with radiological and macroscopic features similar to a meningioma. The unusual location of this tumor and its distinction from meningioma, mucosa-associated lymphoid tissue-type marginal zone B-cell lymphoma of the dura, and intraparenchymal central nervous system lymphoma, dramatically alters the patient's postoperative treatment. The case illustrates the clinical, radiological, and histological relevance of this rare entity.
A 41-year-old Caucasian man with chronic bifrontal headaches and a raised area over his left frontal cranium that persisted for 1 year presented to the emergency room with nausea and vomiting. His family reported that the patient demonstrated increased irritability and aggressive behavior. A computed tomographic scan revealed a large mass of the left frontal convexity with edema and mass effect. Magnetic resonance imaging scans showed a 5-cm homogeneously enhancing mass in the left posterior frontal lobe.
Preoperatively, the patient underwent angiography and embolization of the tumor. The patient underwent gross total resection of tumor. The dural-based tumor invaded the cranium and scalp. Neuropathological findings were consistent with low-grade follicular lymphoma. The patient is currently undergoing radiation and chemotherapy.
The current case represents the first report of extensive intracranial dural involvement by a follicular lymphoma that shows a classic immunophenotype by immunohistochemistry and flow cytometry. The case illustrates the clinical and radiographic similarities between dural-based lymphoma and meningioma. Distinguishing dural-based follicular lymphoma from mucosa-associated lymphoid tissue-type lymphoma and from intraparenchymal primary central nervous system lymphomas, which are more often large cell lymphomas with more aggressive biological behavior, is essential for proper clinical management.
我们报告一例罕见的起源于硬脑膜的滤泡性淋巴瘤,其放射学和大体特征与脑膜瘤相似。该肿瘤的特殊位置及其与脑膜瘤、硬脑膜黏膜相关淋巴组织型边缘区B细胞淋巴瘤和脑实质内中枢神经系统淋巴瘤的鉴别,显著改变了患者的术后治疗方案。本病例说明了这种罕见疾病的临床、放射学和组织学相关性。
一名41岁的白种男性,慢性双侧额部头痛,左额颅骨上方隆起区域持续1年,因恶心和呕吐就诊于急诊室。其家人报告患者易怒和攻击性行为增加。计算机断层扫描显示左额凸面有一个大肿块,伴有水肿和占位效应。磁共振成像扫描显示左后额叶有一个5厘米大小的均匀强化肿块。
术前,患者接受了肿瘤血管造影和栓塞。患者接受了肿瘤全切术。起源于硬脑膜的肿瘤侵犯了颅骨和头皮。神经病理学检查结果与低级别滤泡性淋巴瘤一致。患者目前正在接受放疗和化疗。
本病例是滤泡性淋巴瘤广泛累及颅内硬脑膜的首例报告,免疫组化和流式细胞术显示其具有典型的免疫表型。该病例说明了起源于硬脑膜的淋巴瘤与脑膜瘤在临床和影像学上的相似性。将起源于硬脑膜的滤泡性淋巴瘤与黏膜相关淋巴组织型淋巴瘤以及脑实质内原发性中枢神经系统淋巴瘤(后者更常见为具有更具侵袭性生物学行为的大细胞淋巴瘤)区分开来,对于正确的临床管理至关重要。