>
网站首页期刊介绍通知公告编 委 会投稿须知电子期刊广告合作联系我们
最新消息:
8例外周性原始神经外胚层肿瘤的CT、MRI表现并文献复习
作者:徐朱烽1  靳激扬2 
单位:1. 南京市溧水区人民医院 影像科, 江苏 南京 211200;
2. 东南大学附属中大医院 影像科, 江苏 南京 210009
关键词:外周性原始神经外胚层肿瘤 计算机断层扫描 磁共振成像 病理 免疫组织化学 
分类号:R739.43
出版年·卷·期(页码):2017·36·第三期(403-408)
摘要:

目的:分析外周性原始神经外胚层肿瘤(pPNET)的CT、MRI表现。方法:结合相关文献,对8例pPNET患者的影像学及病理学资料进行回顾性分析。结果:病灶发生于软组织、骨骼、鼻道、内脏,主要表现为浸润性生长的较大软组织肿块,CT呈不均匀等低密度,MRI呈不均匀等长T1等长T2信号,境界不清,易坏死、囊变,无明显钙化,增强强化不均匀,实性成分轻中度强化,囊性成分无明显强化;位于骨骼的pPNET还表现为溶骨性骨质破坏,呈膨胀性改变,无明显肿瘤骨形成及骨膜反应,可继发病理性骨折。结论:pPNET影像学无明显特异征象,需经病理及免疫组化确诊,但影像学检查能清晰地显示病灶的大小、内部结构、毗邻关系、血供情况、侵犯范围及有无远处转移等情况,对治疗及预后具有重要价值。

Objective:To analyze CT and MRI findings of peripheral primitive neuroectodermal tumor(pPNET). Methods:The imaging and pathological features of pPNET in 8 cases were retrospectively analyzed.Results:The lesions were located in soft tissue, bone, nasal passages and viscera, and mainly presented as soft tissue masses with infiltrative growth pattern. CT showed inhomogeneous low density and MRI showed inhomogeneous iso-or hypointensity on T1 WI and iso-or hyperintensity on T2 WI, ill-defined demarcation, necrosis, cystic degeneration, no obvious calcification and heterogeneous enhancement(mild to moderate enhancement for solid components, no significant enhancement for cystic components). pPNET located in bones presented with osteolytic bone destruction and expansile lesion. No obvious tumor bone formation and periosteal reaction were found. Pathological fractures secondary to the tumors occurred. Conclusion:pPNET may present varying imaging features and can only be confirmed by pathological examination and immunohistochemistry. However, CT and MR imaging can clearly show the size of the lesion, internal structure, relationship with adjacent tissues, blood supply, the extent of violations and the distant metastasis, etc., which play key roles in the treatment and prognosis of pPNET.

参考文献:

[1] HART M N,EARLE K M.Primitive embryonalneuroectodermal tumors of the brain in children[J].Cancer,1973,32(4):890-897.
[2] 彭李博,魏雪,时姗姗,等.肺原发原始神经外胚叶肿瘤的临床病理观察[J].医学研究生学报,2015(3):277-279.
[3] 张凤春,唐雷,马越,等.126例外周性原始神经外胚层瘤临床特征及预后因素分析[J].上海交通大学学报:医学版,2012,32(11):1490-1496.
[4] 李世兰,李海,王震.肾脏外周原始神经外胚层肿瘤三例临床病理分析[J].中华病理学杂志,2015,44(11):788-789.
[5] ASHRAF M,BEIGOMI L,AZARPIRA N,et al.The small round blue cell tumors of the sinonasal area:histological and immunohistochemical findings[J].Iran Red Crescent Med J,2013,15(6):455-461.
[6] KOPYS-WISMIEWSKA I.Evaluation of images of periesteum on cmnputedtemography in children with malignant bone tumours before and afterchemotherapy[J].Med Wieku Rozwoj,2008,12(1):463-476.
[7] YAFIGI-RIVARD L,MASSEROT C,LACHENAUD J,et al.Childhood medulloblastoma[J].Arch Pediatr,2008,15(12):1794-1804.
[8] 李明君,郝晓慧,李学章.肺原始神经外胚层肿瘤/尤文氏肉瘤一例[J].海南医学,2015(22):3417-3418.
[9] 田志勇,周怀琪.胃外周型原始神经外胚层瘤1例[J].实用放射学杂志,2013,29(8):1363-1364.
[10] 石军,李凤玉,张海.鼻前庭原始神经外胚层肿瘤一例[J].华北国防医药,2009,21(6):56.

服务与反馈:
文章下载】【发表评论】【查看评论】【加入收藏
提示:您还未登录,请登录!点此登录
您是第 412689 位访问者


copyright ©《东南大学学报(医学版)》编辑部
联系电话:025-83272481 83272483
电子邮件:
bjb@pub.seu.edu.cn

苏ICP备09058364