Yongjun Luo, Xin Liu, Qiu Sun, Jun-Lin Zhou
From the Department of Radiology, The Second Hospital of Lanzhou University, Lanzhou, China.
J Craniofac Surg. 2015 Mar;26(2):e132-7. doi: 10.1097/SCS.0000000000001193.
The purpose of this study was to analyze the imaging findings and clinical features of intracal lymphoplasmacyte-rich meningioma.
The clinical, radiographic, and pathological data of 9 patients of lymphoplasmacyte-rich meningioma were analyzed retrospectively.
All cases were solitary; 8 patients with headache, dizziness, and vomiting; 2 patients with vision loss and one with progressive hearing loss; and 4 cases of secondary anemia, 3 of them with secondary hyperplasia of polyclonal immunoglobulin. In the plain CT scan of 6 cases, all masses showed higher density and without clear boundary, and 5 masses accompany obvious peritumoral edema. In plain MRI scan, all of the tumors appeared with irregular shape and unclear boundaries, 8 of the masses with obvious peritumoral edema. Enhanced scan showed all cases were significantly enhanced and the meninges in 7 cases thicken irregularly and extensively. The pathology showed that the tumors were irregularly shaped with grayish red or grayish white cut surfaces. Histological examination showed that the tumors consisted of abundant and diverse cells and different numbers of spindle tumor cells, and meningeal epithelial cells in the background of abundant inflammatory cells could be seen. The 9 cases all had surgery; only 1 case of recurrence in the first year after the operation was noted in the follow-up over 1 to 4 years, and no recurrence could be found after the second surgery.
Lymphoplasmacyte-rich meningioma is a seldom-seen subtype meningioma of WHO grade I, often accompanying anemia or polyclonal immunoglobulin hyperplasia, which can recover to normal state after removing the masses. The masses showed higher density and without clear boundary in plain CT scan, and most of the tumors appear with irregular shape, obvious edema, and significant enhancement in the MRI scan. The prognosis is favorable after surgical resection and the recurrence rate is low.
本研究旨在分析富含淋巴细胞和浆细胞的颅内脑膜瘤的影像学表现及临床特征。
回顾性分析9例富含淋巴细胞和浆细胞的脑膜瘤患者的临床、影像学及病理资料。
所有病例均为单发;8例患者有头痛、头晕及呕吐症状;2例有视力减退,1例有进行性听力减退;4例有继发性贫血,其中3例伴有多克隆免疫球蛋白继发性增生。6例患者的平扫CT检查中,所有肿块均表现为高密度且边界不清,5个肿块伴有明显的瘤周水肿。平扫MRI检查中,所有肿瘤均呈不规则形且边界不清,8个肿块有明显的瘤周水肿。增强扫描显示所有病例均有明显强化,7例患者的脑膜不规则增厚且范围广泛。病理显示肿瘤呈不规则形,切面为灰红色或灰白色。组织学检查显示肿瘤由丰富多样的细胞以及不同数量的梭形肿瘤细胞组成,在大量炎症细胞背景下可见脑膜上皮细胞。9例患者均接受了手术治疗;在1至4年的随访中,仅1例在术后第一年复发,二次手术后未发现复发。
富含淋巴细胞和浆细胞的脑膜瘤是一种少见的WHO I级脑膜瘤亚型,常伴有贫血或多克隆免疫球蛋白增生,切除肿块后可恢复正常状态。平扫CT检查中肿块表现为高密度且边界不清,MRI检查中大多数肿瘤呈不规则形、有明显水肿且强化显著。手术切除后预后良好,复发率低。