侧脑室肿瘤总结

合集下载

脑室肿瘤诊断要点及鉴别诊断

脑室肿瘤诊断要点及鉴别诊断
• 光镜下表现为单层或柱状立方上皮细胞围绕血管呈均一乳头状排列,无 明显核异形及核分裂相。
脑室肿瘤-脉络丛乳头状瘤
(choroid plexus papillom)
影像学特征
CT平扫: 扩大的脑室内见团块样高密度灶,其内可见斑点钙化;病灶 形态欠规则,分叶状,周边可见结节样改变,颗粒感较明显;增强扫 描呈明显均匀强化,边缘清楚;周围脑实质未见水肿效应(只有肿瘤 较大压迫脑室壁时才导致脑组织水肿效应)。
肿瘤 T1WI 呈稍低信号,T2WI 呈稍高信号,因肿瘤常有囊变、钙化,少数可合 并出血,使信号不均匀,囊变区 T1WI 呈低信号或高信号,T2WI 呈高信号,钙 化灶在 T1WI、T2WI 上一般都呈低信号 。
瘤周水肿效应轻。
脑室肿瘤-室管膜瘤(ependymoma)
脑室肿瘤-室管膜瘤(ependymoma)
脑室肿瘤-中枢神经细胞瘤(central neurocytoma )
CNC影像学特征
常以宽基底与透明隔粘连,累及孟氏孔,引起梗阻性脑积水。 较大的肿瘤常侵犯侧脑室顶壁、侧壁。 肿瘤多呈囊实性;增强扫描后实性部分明显强化,囊变区无强化。
肿瘤周边或内部可见流空血管影。 瘤周水肿罕见。 MRS 发现高甘氨酸伴高丙氨酸峰或者肌醇峰伴高丙氨酸峰对诊断有较高价值。
脑室肿瘤-室管膜巨细胞星形细胞瘤
(subependymal giant cell astrocytoma SEGA)
脑室肿瘤-脉络丛乳头状瘤
(choroid plexus papillom)
脉络丛乳头状瘤属良性肿瘤,起源于脉络上皮细胞,是一种少见的 肿瘤,占颅内肿瘤的0.4%~0.7%,占胶质瘤的2%。占儿童颅内肿 瘤的1.8%~3% 约45%的脉络丛乳头状瘤患者在1岁内发病 74% 在10岁以内发病。

侧脑室脑膜瘤MRI诊断价值

侧脑室脑膜瘤MRI诊断价值
准确 性 。
3 1 肿瘤的发生、 . 临床 特点及 病理
脑膜 瘤为 常见 的颅 内肿
瘤, 多数为 良性病变 , 多位 于大脑 凸面、 大 大脑镰 旁 、 状窦旁 、 矢
前颅窝底 嗅沟区、 蝶骨嵴等部 位 , 而侧脑 室内脑膜瘤较 为少见 ,
占所有颅内脑膜瘤 的 0 3 一 .% … 。一 般认为起 源于脉 络 .% 5O 丛组织或脉络丛基 质 , 发于 脑室 内脉络丛 分布 丰富 的区域 , 好
膜瘤 的 M I 现具有一定的特征性 , R表 结合 临床 资料 可提 高诊 断的准确性 。
【 关键词 】 磁共振成像 ; 室; 侧脑 脑膜瘤 ; 诊断 【 中图分类号】 R794 【 3.5 文献标识码】 A
【 文章编号】 1 2 78 (02 0 — 38 0 0 — 36 2 1)3 07 — 3 0
龄在 3 O~6 o岁 , 女性 较男性 多见 J 本组性 别均 为女性 , 1 , 除
描仪 , 采用标准头 颅线 圈 ,O 8 F V 17mm×2 0m 矩 阵 24X 3 m, 3 3 4 扫描层厚 5mm, 8, 层间距 15mm。采用 s . E序列行横 断面 、
38 7
可 医药 2 1 北 0 2年 2月 第 3 4卷 第 3 期
H b i dcl o ra,0 2 V l 4F bN . ee Mei u l 2 1 , o 3 e o3 aJ n
d i1 .9 9 ji n 1 0 7 8 .0 2 0 .3 o:0 3 6/ . s .0 2— 36 2 1 .3 0 0 s

论 著

侧 脑 室脑 膜 瘤 MR 诊 断价 值 I
赵 亮 【 摘要】 目的 研究侧脑室内脑膜瘤的 M I R 表现特点, 高诊断的准确性。方法 提

脑室内肿瘤影像诊断

脑室内肿瘤影像诊断
精选课件
精选课件
精选课件
精选课件
ependymoma
精选课件
精选课件
精选课件
精选课件
室管膜下室管膜瘤 subependymoma
• 室管膜下室管膜瘤是一类罕见的、生长 缓慢的良性肿瘤, 属于Ι级,多无临床症 状,仅于尸体解剖时偶然发现,但当肿 瘤阻塞脑脊液通道时则产生临床症状, 多发生于中老年人
• 可发生于脑室系统通道上的任何部位, 但以侧脑室和第4脑室最为常见
精选课件
室管膜下室管膜瘤
• 肿瘤组织分类将其归为室管膜肿瘤,该 肿瘤在大片胶质纤维的构成中可见成簇 的大小一致的室管膜细胞
• 幕上室管膜下室管膜瘤钙化相当少见, 而幕下者钙化很常见;
• 幕上室管膜下室管膜瘤血供差,大的肿 瘤还经常可以见到陈旧性出血及含铁血 黄素沉着
• 由室管膜上皮外面的一层星形细胞长出 的肿瘤,称室管膜下巨细胞星形细胞瘤。 临床少见,在15%的结节硬化患者病人 中发生这种肿瘤。患者多为儿童,肿瘤 的恶性度为I级,成人也可患病,但预后 较儿童差,肿瘤的恶性度为 级。
精选课件
• 大多数肿瘤发生于室间孔附近, • CT平扫为等密度或略低密度的肿块,瘤
• 等密度或稍高密度 • MRT1等或稍低信号,T2稍高信号 • 因囊变坏死钙化密度信号常不均质 • 境界清楚,常见轻度分叶 • 显著均质或不均质强化 • 脑脊液分泌过多,脑室扩大
精选课件
诊断和鉴别诊断
• 儿童应和脉络丛乳头状癌、乳头状室管 膜瘤、髓母细胞瘤、星形细胞瘤等鉴别。
• 成人主要应和脑膜瘤、转移瘤鉴别。
精选课件
choroid plexus papilloma
精选课件
精选课件
精选课件
精选课件

9例侧脑室三角区脑膜瘤的诊治体会

9例侧脑室三角区脑膜瘤的诊治体会

[ ] Moa G, n hm T,rs J e 1Vau m- stdcm lx 3 rn S Wid a S Cos M,t . cu a i e o pe a ss
wo n l s r t ls i e s l lo u me tt n o e e h u d co u e wi ea tc v se o p a g n a o .a n v l tc — h i
15 结果 . 所有 病例 均镜 下全 切 除 , 手术 死 亡病例 。病 无
脑 室 系 统 脑 膜 瘤 起 源 于 脉 络膜 或 脉 络 丛 的蛛 网膜 细
胞 , 占颅 内脑膜瘤的 25 ~ .% , 约 .% 63 其中大部分位于侧脑 室, 而侧 脑室 脑膜 瘤 又大部 分位 于 三 角 区及 其 附 近…。 20 06年 9月至 2 1 00年 1 0月我们共收治了 1 例侧脑室脑 1 膜瘤患者 , 中9例肿瘤主体位于侧脑室三角区, 其 均采用显
微创 医学 21 02年第 7 第 1 卷 期
Ju a o n l vs eMei n ,0 27 1 or l f i l I ai dc e2 1 ,( ) n Mi may n v i

81 ・
负压 的有 效性 , 防止创 面 因处 于封 闭 无负 压 的环 境 中 , 而导 致感 染恶 化 。创面 感 染 或 炎性 分 泌 物 多 , 导 致 引 流 管堵 易 塞, 使负 压封 闭引 流 失败 。采 用 “ 闭 技术 ” 有效 防止 夹 能 因 中心负压 不够 导 致 引 流 不 畅而 使 治疗 失败 : 闭一 部 分 夹 管 道 , 另一 部分 足够 的负压 吸 引 , 替进 行 。⑦创 面较 保证 轮
肤撕脱伤的体会[ ] 生物骨科材料 与临床研究 ,09 6 1 :1 J. 20 , ( )4

侧脑室内脑膜瘤的临床特点和手术策略

侧脑室内脑膜瘤的临床特点和手术策略
脑 膜瘤 发 病率 更 低 ,但 多数 位 于侧 脑 室 内_ 3 _ 。本组
病例 较少 未有 明显 差异 。
形均质 高密度或稍 高密度影 ,2 向同侧枕 角延 例 伸 ,1 主要位 于颞 角 ,另有 2 累及侧脑 室体 例 例
部 ;1 见 点状 钙化 ,同侧 脑 室颞 角 和枕 角不 同程 例 度 的扩 大 ;4例肿 瘤 周 围脑组 织 有 低 密 度 水 肿 带 , C T增 强 扫描 后 中度 强化 ,2例病 灶 中心 强 化 不均 。 MR 表 现 为 ,T WI 病 变 侧 侧 脑 室 受 压 与 移 位 , I 1 呈
月 21 00年 1 月采用显微手术方法治疗侧脑室脑 1 膜瘤患者 1 例 ,现就诊断及治疗体会报告如下。 1 资 料 与 方法 1一般 资 料 :本 组 1 例 ,男 5 . 1 例 ,女 6 。年龄 1 ~ 2 ,平均 4 .岁。病程 例 3 6岁 1 2 7 个月 6 年。病灶位 置 :左侧脑室 7例 ,右侧脑 室 4 ,其 中位 于侧脑 室三角区 8例 ,三角区累 例 及枕角 2 ,颞角 1 ,体部 2 例 例 例。 2 . 临床表现 :本组病例均有不 同程度 的阵发性 头 痛 ,以胀 痛 为 主 ,部 位 不 定 ,以 双额 或颞 侧 多 见 ,部分 头痛 与体位有关 ;恶心呕吐 5例 ;视物
对 肿瘤的逐渐生长有代偿作用 ,局部症状 出现较
少 ,早 期 缺乏 定 位 体 征 ,一 般 病 程 较 长 。肿 瘤 生
长较大时将产 生 占位效应 或影 响脑脊液循环 引起 高颅压症状 和周 围脑组织受压症状 ,表现为进行 性 加重的头痛和视乳头水肿 ,由于肿瘤在脑室 内 有一定活动度 ,因而可产生活瓣 作用 ,尤其是位
脑室脑膜瘤来源于异位至脉络丛 、脉络组织及侧 脑 室壁 的蛛 网膜 细胞 Ⅲ ,属 少见 的脑 膜瘤 ,由于 三 角区的脉络丛丰富 ,所以 7 %~ 0 0 8%的侧脑室脑膜 瘤位于三角区 ,也可以向颞角 、枕角和体部延伸 , 其 供血 主 要来 自脉 络膜 前 动脉 和 或脉 络 膜后 动 脉 , 成人较儿童多见 ,女性多于男性 ,左侧多于右侧。 有 学 者 认 为 侧 脑 室 脑 膜 瘤 发病 以 女性 多见 ,儿 童

侧脑室肿瘤诊治分析(附32例报告)

侧脑室肿瘤诊治分析(附32例报告)

31 诊 断 .
由于脑 室内充பைடு நூலகம் 脑脊 液 , 对肿瘤 的发展有一定 的
水 1 例 。临床症状 : 痛 3 1 头 0例 , 吐 2 呕 5例 , 视力 障碍 7例。 双眼底视乳头水肿 1 , 1例 视乳 头萎缩 3例 。同 向偏 盲 1例。 眼球 外 展 受 限 2例 , 枢 性 面 瘫 1例 , 体 偏 瘫 5例 。偏 身 感 中 肢 觉 障碍 1 。辅 助 检 查 :2例 均 行 头 颅 C 例 3 T扫 描 , 行 脑 电 6例 图检查 。所有 患者者术前均 行 MR 检查 。肿瘤直 径大小 : I < 2e 5例 , 4c 2例 , 4 c 。 m 1 2~ m 1 > m 5例 12 治 疗 方 法 根 据 肿 瘤 生 长 部 位 , 开 重 要 功 能 区 行 肿 瘤 . 避 切 除术 。其 中经皮质入 路 1 , 胼胝 体入路 l 9例 经 3例。切开 脑皮质 , 自动牵开器牵开 脑组 织进入侧 脑室 。在脑 室 内肿瘤 周 围盖 以棉 片 , 保护侧脑室壁及室 间孔 附近静脉等重要结 构。 减少 对脑组织 的牵拉 , 根据肿瘤 的大小 和性 质采取 不同 的方 法切 除肿瘤 。瘤体 > m者宜 先作瘤 内分块切 除肿瘤 , 2c 待体 积缩小后将瘤 壁完全 切除 。瘤 体 <2c m者 可整 个切 除 。有 囊变者先穿刺抽 出囊液 , 再切开囊壁 , 分块 切除。胶 质瘤常分 界不 清 , 在尽 可能不损 伤重要 神经核 团和 血管 的情 况下作镜 下 全 切 除 , 侵 犯 的 脑 室 壁 也 应 一 并 切 除 。对 于供 血 较 丰 富 被 的肿瘤 , 尽可能早地暴露并 切 断肿 瘤 的供血动 脉 , 减少 出血 , 保 持 术 野 干净 。术 后 脑 室 内 常规 留 置 引 流 管 。

侧脑室脑膜瘤的MRI表现

侧脑室脑膜瘤的MRI表现

侧脑室脑膜瘤的MRI表现摘要】目的:探讨侧脑室脑膜瘤的MRI表现,并结合文献,提高对该病的诊断及鉴别诊断水平。

方法:回顾分析15例经手术和病理证实的侧脑室脑膜瘤的MRI 表现。

结果:15例中,年龄最小13岁,最大58岁,平均33岁,其中女性14例(14/15),男性1例(1/15)。

肿瘤以侧脑室三角区多见,本组14例(14/15),侧脑室体部1例(1/15)。

例病理均为WHOⅠ级,其中纤维型12例(12/15),纤维上皮型1例(1/15),血管瘤型脑膜瘤1例(1/15),过渡型1例(1/15)。

结论:侧脑室脑膜瘤的MRI表现有一定的特征性,结合临床及发病部位、年龄、性别可提高诊断准确率。

【关键词】脑膜瘤;侧脑室;磁共振成像;诊断【中图分类号】R445 【文献标识码】A 【文章编号】2095-1752(2016)29-0185-02脑膜瘤是颅内常见肿瘤之一,仅次于胶质瘤而居第二位,为颅内最常见良性肿瘤,约占颅内肿瘤的15%~20%,其中侧脑室脑膜瘤较少见,但却是成人最常见的脑室内肿瘤[1]。

笔者收集了15例侧脑室脑膜瘤的MRI资料,对其MRI表现进行分析,以提高对该肿瘤的诊断。

1.材料与方法1.1 临床资料回顾性分析整理了2009年至2012年进行MRI检查且经术后病理证实的15例侧脑室脑膜瘤患者的资料,其中男1例,女14例,年龄13~58岁,平均年龄33岁。

临床表现主要为颅高压症状,包括头痛、呕吐、视盘水肿等,而神经系统损害不明显。

所有病例均经手术病理证实,并有完整MRI资料。

1.2 检查方法采用1.5T或3.0T超导型磁共振成像仪,均行MRI常规平扫、增强扫描检查,包括横轴位、矢状位及冠状位。

增强扫描用钆喷替酸葡甲胺(GD-DTPA),剂量0.1mmol/kg体重,注射流率3ml/s,经肘静脉注射。

9例行DWI,采用SE-EPI序列,加频率选择脂肪抑制技术,行横轴面成像,扫描参数为:TR7000ms,TE80ms,b值取0s/mm和1000s/mm,矩阵128×128。

侧脑室内肿瘤的显微外科治疗(附28例报告)

侧脑室内肿瘤的显微外科治疗(附28例报告)

mir s r ey i u o p tl r m e t mb r 2 0 oJ n , 0 9 we ea ay e e r s e t ey i cu i gt e ci i a au e , ig o i, e o u g r no r s i o S p e e , 0 2 t u e 2 0 , r n l z d r t p c i l , n l d n l c l e tr s d a n s h af o v h n f s
周 旺宁 张建 生 张新 定 韩彦 明 程得钧
【 摘要 】目的 探讨侧脑室 内肿瘤 的临床特征和个体化显微手术策略及疗效 。方法 回顾性分析 2 0 年 9 02 月至 2 0 年 6 09 月手
术治疗并经病理证实的 2 例侧脑室内肿瘤患者的临床资料 。结果 肿瘤全切除 2 例 , 8 2 次全切 3 , 例 大部分切 除3 。经病理学证 例 实室管膜瘤 8 , 例 脉络丛乳头状瘤 4 , 例 脑膜瘤 6 , 例 少枝胶质细胞瘤 4 , 例 星形细胞瘤 3 , 例 中枢神经细胞瘤 2 , 例 胶质母细胞瘤 1 例。1 因术后硬膜下血肿再次手术 , 例因脑积水而行脑室一腹腔分流术 , 例术后出现颅内感 染 , 例因严 重感 染并脑积水死 例 7 5 1 亡。术后 配合 放疗 和/ 或化疗 1 例 。术后 随访 6 月至 3 , 例轻残 ,0 9 个 年 2 1 例生活 自理 ,5 1 例可参加 日常工作 。结论 侧脑室 内肿
a d te t n ft e lt r l e t ce t mo s a d t a me to to s Re u t 8 p t n swi ae a e t ce t mo ,2 e e v d n r ame t ae a n r l u r n e t n u c me . s l Of2 a i t t ltr lv n r l u r 2 rc i e o h v i r s e h iБайду номын сангаасs t tl r s c in o h u r ,3 s b oa a d 3 p ri1 h p t oo i a x mi ai n p o e h t o 8 p t ns u fr d fo oa e e t f t e t mo s u tt o l n a t .T e ah lg c l e a n t r v d t a f 2 ai t,8 s f e r m a o e e e e d mo s h r i s lx s a i 0 s me i go s oi o e d 0 o s a to y o s 1 l b a tma a d c nr l p n y ma ,4 c o od p e u p p l ma , l 6 n n ima ,4 l d n r ima , g 3 sr c t ma , gi l s o o n 2 e t a n u o yo s On p t n d e f m p so e a ie n rc a il n e t n n h d o e h u , Ni ee n e ev d o t p r t e e r c t ma . e ai t id r e o o t p r t i ta r na i fc i a d y r c p a s v o l n te r c ie p so e ai v
  1. 1、下载文档前请自行甄别文档内容的完整性,平台不提供额外的编辑、内容补充、找答案等附加服务。
  2. 2、"仅部分预览"的文档,不可在线预览部分如存在完整性等问题,可反馈申请退款(可完整预览的文档不适用该条件!)。
  3. 3、如文档侵犯您的权益,请联系客服反馈,我们会尽快为您处理(人工客服工作时间:9:00-18:30)。

J Neurosurg 88:581–585, 1998Multiple choroid plexus papillomas of the lateral ventricle distinct from villous hypertrophy侧脑室多发脉络丛乳头状瘤FIG. 1. Axial T1-weighted MR images revealing slightly hypointense to isointense lesions in the right atrium and left inferior horn of the lateral ventricles (upper), and Gd-DTPA–enhanced images demonstrating a marked homogeneous enhancement of the lesions (lower).平扫及增强影像。

FIG. 2. Sagittal T1-weighted MR images with Gd-DTPA enhancement clearly revealing the anatomical relationship between the tumors and the surrounding structures, which marked their location more easily. Left: Sagittal images of the left side of brain. Center: Sagittal image of the center of brain. Right: Sagittal images of the right side of brain.FIG. 3. Upper: Photomicrograph of the tumor specimen obtained during the first operation in the right ventricular region. Note the papillary growth of a single and partly stratified layer of columnar epithelium, consistent with a typical choroid plexus papilloma. Lower: Photomicrograph of the tumor specimen obtained during the second operation in the left ventricular region. The histopathological characteristics are similar to those shown in the right ventricular region. H & E, original magnification 3 200.病理结果。

Acta Neurochir (2003) 145: 139–143 DOI 10.1007/s00701-002-1047-x Acta Neurochirurgica Printed in Austria Case ReportChoroid plexus papilloma of bilateral lateral ventricleT. Erman1, A. I˙. Go¨c¸er1, S¸ . Erdog˘an2, M. Tuna1, F. I˙ldan1, and S. Zorludemir21Department of Neurosurgery, C¸ ukurova University, School of Medicine, Adana, Turkey2Department of Pathology, C¸ ukurova University, School of Medicine, Adana, TurkeyFig. 1. (a) Axial non-contrast CT scan demonstrating tumour of the lateral ventricles bilaterally and hydrocephalus. (b) Axial contrast enhanced CT scan demonstrating an enhancing tumour of the lateral ventricle bilaterally with hydrocephalus(b) Axial contrast enhanced CT scan demonstrating an enhancing tumour of the lateral ventricle bilaterally with hydrocephalusFig. 2. Axial enhanced MRI demonstrating a lobulated enhancing mass in the bilateral lateral ventricular trigoneFig. 2. Axial enhanced MRI demonstrating a lobulated enhancing mass in the bilateral lateral ventricular trigoneTransient memory disturbance after removal of an intraventricular trigonal meningioma by a parieto-occipital interhemispheric precuneus approach:Case report肿瘤切除后记忆暂时紊乱Koji Tokunaga, MDa,T, Takashi Tamiya, MDb, Isao Date, MDaaDepartment of Neurological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, JapanbDepartment of Neurological Surgery, Faculty of Medicine, Kagawa University, Kagawa 700-8558, JapanReceived 15 December 2004; accepted 13 June 2005Fig. 1. Left and center: Preoperative gadolinium-enhanced T1-weighted MR images demonstrating a homogeneously enhanced mass at the left trigonal region, extending predominantly in the anterior direction. Right: A T2-weighted MR image showing moderateedema around the massFig. 2. Left and right: Postoperative gadolinium-enhanced T1-weighted images demonstrating the route approaching the left trigone from the interhemispheric fissure and confirming complete removal of the tumorSymptom Changes Caused by Movement of a Calcified Lateral Ventricular Meningioma CASE REPORTShigeki Imaizumi, M.D.,* Takehide Onuma, M.D.,* Motonobu Kameyama, M.D.,* and Kiyoshi Ishii, M.D.†*Departments of Neurosurgery and †Radiology, Sendai City Hospital, Sendai, JapanSequential CT studies over 16 years revealed no distinctive change in size of the calcified meningioma (A-D). CT taken 16 years before this admission (A). Hydrocephalus and peritumoral edema caused by a tumor in the ventricle were seen at admission (B). The ventricle size was normalized after ventriculoperitoneal shunt placement (C). The tumor was displaced beyond the ventricular midline five months later (D). Half of the tumor was resected during the 1st surgery using the trans callosal route (E) and the remaining mass was removed during the second surgery using the trans inferior temporal sulcus approach (F).Hemangiopericytoma in the Trigone of the Lateral Ventricle—Case Report—Fig. 1 Axial computed tomography scan showing a massive right tri gonalmass, with dilation ofthe contralateral ventricle.Fig. 2 (A) Preoperative axial T1-weighted magnetic resonance (MR) image showing a large, isointense trigonal tumor. (B) T2-weighted MR image showing the hypointense tumor. (C) Sagittal T1-weighted MR image with contrast medium showing intense enhancement of the tumor.Neurol Med Chir (Tokyo)Child’s Nerv Syst (1998) 14:350–353© Springer-Verlag 1998 BRIEF COMMUNICATIONMeningiomas of the lateral ventricles of the brain in childrenFig. 1 MRI showing intraventricular massFig. 2 CT 2 weeks after operation, showing complete removal of tumour Fig. 3 CT scan showing intraventricular neoplasm in trigone region Fig. 4 CT 6 months after operation, showing complete removal of tumourActa Neuropathol (Berl) (1986) 71 : 167-- 170 ActaNeuropathologlca9 Springer-Verlag 1986Central neurocytoma - a rare benign intraventricular tumorj . j . Townsend I, 2 and J. P. Seaman 3Department of Pathology, University of Utah2 Salt Lake Veterans Administration Medical Center3 LDS Hospital, Salt Lake City, UT, USAFig. 1. This picture demonstrates the well-circumscribed soft tumor mass (in the anterior right lateral ventricle) attached to the septum pellucidum and corpus callosum (case 1)Fig. 2. The CT scan demonstrates the well-circumscribed mass in the right lateral ventricle anteriorly producing hydrocephalus (case 2)Fig. 3. This print demonstrates the tumor to be composed of small dark nuclei forming occasional Homer Wright rosettes as seen in the center of the picture (case 1). Hematoxylin and eosin, x 800Fig. 4. The tumor was composed of small round to oval nuclei which formed Homer Wright rosettes as seen in the center (case 2).Hematoxylin and eosin, x 375Fig. 5. The neurosecretory granules can be seen in this electron micrograph, x 27,173Fig. 6. Electron microscopy demonstrated numerous synapses with well-formed junctions as seen in the center, x 27,173Journal of Clinical Neuroscience (1999) 6(4), 319-323© 1999 Harcourt Brace & Co. LtdClinical studiesIntraventricular neurocytoma: a clinicopathological study of 20 cases with review of the literatureMehar Chand Sharma ~ MD, Chitra SarkaP MD, Asis Kumar Karak ~ MD PHD, Sailesh Gaikwad 2 MD,Ashok Kumar Mahapatra a MCH, Veer Singh Mehta a MCHFig. 1 Contrast enhanced CT scan showing a well defined hyperdense mass, predominantly in the right lateral ventricle with cyst formation and secondary hydrocephalus (Case 16).Fig. 2 Photomicrographs showing: (A) cellular areas separated by acellular fibdllary zones (H&E x 350); (B) thin walled dilated vascular channels within the tumour (H&E × 140); (C) diffusefibrillary immunostaining with synaptophysin antibody (x 200)Case reportEpidermoid of the lateral ventricle: evaluation with diffusionweighted and diffusion tensorimaging表皮样囊肿Radboud W. Koot a, Anuradha P. Jagtap b, Erik M. Akkerman b, Gerard J. DenHeeten b, Charles B.L.M. Majoie b,*a Department of Neurosurgery, Academic Medical Center, P.O. Box 22660, 1100 DD Amsterdam,Netherlandsb Department of Radiology, Academic Medical Center, P.O. Box 22660, 1100 DD Amsterdam,NetherlandsReceived 4 March 2003; accepted 14 March 2003Fig. 1. (A, B, C): (A) Axial T2-weighted (3500/90/1), and axial (B) and coronal (C), contrastenhanced T1- weighted (570/40/2) MR images show enlarged left lateral ventricle with masseffect and shift of midline structures to the right. Note widening of the left choroidal fissure (C;arrow). A definite tumor cannot clearly be delineated. (D, E) Axial DWI shows a hyperintenselesion in the left perimesencephalic cistern (D; arrow) and in the dilated left lateral ventricle (E).The mass is surrounded by hypointense CSF. Findings are consistent with epidermoid tumor. (F) ADC map at the same level as (E) show ADC values in the lesion similar to brain parenchyma.(G) FA maps of the lesion show areas of anisotropy, clearly demonstrate its relationship to neighboring white matter tracts and accentuate the lobulated structure of the lesion (tensor-imaging).Fig. 1. (A, B, C): (A) Axial T2-weighted (3500/90/1), and axial (B) and coronal (C), contrast enhanced T1- weighted (570/40/2) MR images show enlarged left lateral ventricle with mass effect and shift of midline structures to the right. Note widening of the left choroidal fissure (C; arrow). A definite tumor cannot clearly be delineated. (D, E) Axial DWI shows a hyperintense lesion in the left peri mesencephalic cistern (D; arrow) and in the dilated left lateral ventricle (E). The mass is surrounded by hypointense CSF. Findings are consistent with epidermoid tumor. (F) ADC map at the same level as (E) show ADC values in the lesion similar to brain parenchyma.(G) FA maps of the lesion show areas of anisotropy, clearly demonstrate its relationship to neighboring white matter tracts and accentuate the lobulated structure of the lesion(tensor-imaging).A large arachnoid cyst of the lateral ventricle extending from the supracerebellar cistern—case reportSeoung Woo Park, MDa, Soo Han Yoon, MDb,*, Ki Hong Cho, MDb, Yong Sam Shin, MDbaDepartment of Neurosurgery, Kangwon National University, College of Medicine, Chunchon 200-701, South Korea bDepartment of Neurosurgery, Ajou University School of Medicine, Suwon 443-721, South KoreaReceived 23 May 2005; accepted 30 July 2005Fig. 1. Initial MRimaging shows that the arachnoid cyst had developed from the supracerebellar space in the posterior fossa and extended into the antrum and temporal horn of the left lateral ventricle. A and B: Axial MR imaging shows that the intraventricular cyst displaces the left choroidal vessels anteriorly (small arrow heads), the right choroid plexus laterally (smallarrow), the midline vessels to the right (large arrow), and an enlarged velum interpositum. C: Axial MR imaging shows that the left choroid plexus (small arrow) was severely displaced anteriorly and the thin cystic wall (arrow head)crossed the right lateral ventricle. D and E: CoronalMRimages show that the cyst (small arrow heads) displaces the left choroids plexus contralaterally (arrow) and the right choroid plexus and choroidal vessels laterally (large arrow head). F: Coronal MR images shows displaced and collapsed right choroids plexus (small arrow), branching portion of choroidal vessels (large arrow), and left choroidal vessels (arrow head). G: Sagittal MR imaging shows that the cyst of the posterior fossa depressing the cerebellum downwardly (arrows) extending into and dilating the velum interpositum (small arrow heads) with anteriorly displaced contralateral choroid plexus (large arrow). H: Sagittal MR imaging shows the herniation of cerebellum (arrow) with visualization of the central canal of the cervical spinal cord (arrow heads).Clinical StudyIntraventricular tanycytic ependymoma: case report and review of the literatureBrian T. Ragel1, Jeannette J. Townsend2, Adam S. Arthur1 and William T. Couldwell11Department of Neurosurgery; 2Department of Pathology, University of Utah Health Sciences Center, Salt Lake City,UT, USAKey words: supratentorial tumors, tanycytic ependymomaFigure 1. Brain MRI depicting 2.8 · 2.6 · 2.3 cm (height · transverse · anterior–posterior) lesion arising from the region of the left superolateral third ventricle and septum pellucidum. Mass extends superolaterally into the left frontal horn of the lateral ventricle. (A) Axial T1 with contrast, showing minimal enhancement. (B) Axial T2, showing heterogenous signal. (C) Coronal T1 with contrast, with incidental left sphenoid wing meningioma (arrow). (D) Coronal FLAIR sequence.Figure 2. (A) Low-power H&E stain (150·) showing moderately cellular tissue with areas of well-differentiated streaming tumor cells set in a vague fascicular architecture and faint perivascular pseudorosettes (black arrow). (B) High-power H&E photomicrograph (300X) depicting tumor cells arranged radially around a blood vessel, typical of the perivascular pseudorosettes of ependymomas (black arrow). (C) High-power photomicrograph (600X) of GFAP immunohistochemistry reactivity, depicting the delicate GFAP-positive processes of ependymal cells radiating towards the blood vessel wall (black arrow).Shunji Nishio · Takato Morioka · Futoshi MiharaMasashi FukuiSubependymoma of the lateral ventriclesFig. 1 Case 1. Enhanced CT scan shows a low density tumor in the right lateral ventricleFig. 2A–C Case 3. On contrast enhanced axial T1-weighted image, a hypointenseintraventricular tumor shows no tumor enhancement. Note cystic areas within the tumor and associated hydrocephalus (A). While the tumor is indistinguishable from the cerebrospinal fluid in the ventricle on T2-weighted image (B), it is clearly distinguished on heavily T2-weighted image (C)Fig. 3A–C Case 4. Axial T1-weighted precontrast MRI shows a hypointense tumor filling the anterior horn of the right lateral ventricle (A). A T2-weighted MRI shows peritumoral edema in the right frontal lobe (B). Axial T1-weighted postcontrast MRI shows heterogeneous enhancement of the tumor (C)Massive symptomatic subependymoma星状细胞增生性室管膜瘤of the lateral ventricles: case report and review of the literature大的症状性瘤Fig. 1 Axial pre- (a) and post- (b) contrast-enhanced computed tomography (CT) of the head shows a large symmetric isodense intraventricular mass without calcifications filling the lateral ventricles and extending into the temporal hornsFig. 2 Axial T2-weighted and fluid attenuation inversion recovery (FLAIR) images (b, c) show a large symmetric hyperintense intraventricular mass that fills the lateral ventricles (a, b) and the temporal hornsFig. 3 Axial (a) and coronal T1-weighted (b) post-contrastenhanced images demonstrate an intraventricular mass with minimal enhancement occupying the lateral ventricles and extending into the temporal hornsFig. 5 Axial T2-weighted (a),FLAIR (b), and T1-weighted(c) post-contrast-enhancedimages demonstrate a slight debulking of the tumor after surgery with CSF present in the frontal horns of the lateral ventricle. The patient has a right frontal ventriculoperitoneal shunt catheter in place and is presently asymptomaticFig. 4 Resection specimen reveals a subependymoma, as characterized by nests of tumor cell nuclei and microcysts in a fibrillary stromaMulticentric juvenile pilocytic astrocytoma occurring primarily in the trigone of the lateral ventricleFig. 1 A Pre- and B post-contrast enhancement computerized tomography showing a7´6´6 cm mixed-density mass in the trigone of the left lateral ventricle entrapping the ipsilateral occipital horn. The solid compartment and cystic wall are well enhanced. There were conglomerate calcifications in the posteromedial portion of the mass. Hydrocephalus is also noted Fig. 2A–D Preoperative magnetic resonance images (MRIs). A Axial T1-weighted MRI showing a mixed-intensity mass with sharp demarcation from the adjacent structures except the posteromedial portion of the mass. B–D Gadoliniumenhanced MRIs showing that the cystic wall and solid component are well enhanced and that the septum pellucidum and lateral ventricular wall, the perimesencephalic cistern, and the anterior meninges or ventral aspect of the brain stem are enhanced, suggesting leptomeningeal spread. Small enhanced nodules are also seen in the right anterior temporal and occipital lobes as nodular disease. Tonsillar herniation and mild distortion of the brain stem with enlargement of the IV ventricle are also shownFig. 3 Photomicrograph of the trigonal juvenile pilocytic astrocytoma showing the typical histological features, including pilocytic, stellate, and oligodendroglial cells, microcysts, cytoid or granular bodies, and Rosenthal fibers with loose and compact areas. Vascular proliferationand pleomorphism are absent. (H & E, ´250)Intraventricular HemangiopericytomaNabeel Al-Brahim, MD, Rocco Devilliers, MD, FRCS(C), andJohn Provias, MD, FRCP(C)Figure 1. Axial T1-weighted magnetic resonance image shows a well delineated tumor in the right lateral ventricle.Figure 2. Contrast-enhanced T1-weighted image shows homogenous enhancement of the tumor.Figure 3. Cellular tumor with slitlike vasculature, some with stag horn appearance. (Scanning magnification.)Mixed malignant germ cell tumour of the lateral ventricle in an 8-month-old girl: case report and review of the literatureFig. 1 MRI scan showing contrast- enhancing tumour masses in both lateral ventricles with a big cyst located in the left lateral ventricle Fig. 2 MRI scan showing considerablereduction in tumour volume after four cycles of chemotherapy Fig. 3 MRI scan demonstrating no tumour 14 months after initial diagnosisMature Teratoma of the Lateral Ventricle: Report of Two Cases成熟畸胎瘤M. SelcËuki1, A. Attar1, N. YuÈceer1, H. Tuna1, and E. CË akõrogÆlu21 Division of Pediatric Neurosurgery, Department of Neurosurgery, University of Ankara, School of Medicine, Ankara, Turkey, and2Department of Pathology, AtatuÈrk Chest Diseases and Thoracic Surgery Center, Ankara, TurkeyFig. 1. Preoperative axial enhanced CT shows a mass of the lateral ventricleFig. 3. Mature adipose tissue including nonstriated muscle bundles and tubular structures lined by tall columnar ciliated cells (HE, 200).Case Report: Craniospinal Cysts An endoscopically proven ventriculitis-type, cyst-like intraventricular primary lymphoma of the central nervous systemFig. 1. Magnetic resonance imaging shows a 43 3 cm cystic mass in the frontal horn of the left lateral ventricle. The cyst wall (white arrows) appeared as high intensity in T1-weighted images with gadolinium enhancement on the axial view (a). This cystic mass (white arrows) in the left lateral ventricle was attached to the medial and inferior ventricular wall around the foramen of Monro on the coronal and sagittal view (b, c). There was no parenchymal or leptomeningeal enhancementFig. 1. Magnetic resonance imaging shows a 43 3 cm cystic mass in the frontal horn of the left lateral ventricle. The cyst wall (white arrows) appeared as high intensity in T1-weighted images with gadolinium enhancement on the axial view (a). This cystic mass (white arrows) in the left lateral ventricle was attached to the medial and inferior ventricular wall around the foramen of Monro on the coronal and sagittal view (b, c). There was no parenchymal or leptomeningeal enhancementFig. 1. Magnetic resonance imaging shows a 43 3 cm cystic mass in the frontal horn of the left lateral ventricle. The cyst wall (white arrows) appeared as high intensity in T1-weighted images with gadolinium enhancement on the axial view (a). This cystic mass (white arrows) inthe left lateral ventricle was attached to the medial and inferior ventricular wall around the foramen of Monro on the coronal and sagittal view (b, c). There was no parenchymal or leptomeningeal enhancementFig. 3. Pathological examination showed non-Hodgkin’s lymphoma of B cell type, showing microscopically infiltrating lymphocytes along the perivascular spaces and small vessel walls with positive immunochemical staining for CD20 (white arrows)。

相关文档
最新文档