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1.
目的:探讨CT对卵巢纤维瘤的诊断价值。方法:回顾性分析11例(12个肿块)卵巢纤维瘤的临床及CT表现。结果:11例(12个肿块)中4例见腹腔积液,1例瘤内出血。CT表现:(1)单纯肿块型6例,表现为密度均匀的实性肿块,不强化或轻度强化;(2)囊状变性型4例,肿块边界清晰,内有圆形或不规则形低密度影,增强扫描肿瘤实性成分无明显强化或轻度不均匀强化,低密度区无强化;(3)血管扩张型1例,表现为肿瘤明显持续强化。结论:卵巢纤维瘤的CT表现有一定特征性,多表现为附件区的实性肿块,呈轻度强化或不强化,有助于与其他卵巢肿瘤鉴别。  相似文献   

2.
目的 探讨儿童纵隔神经母细胞瘤的CT与MRI表现及其诊断价值.方法 回顾性分析21例经病理证实的儿童纵隔神经母细胞瘤的CT和MRI表现.19例行CT检查,8例行MRI检查.结果 20例肿瘤位于后纵隔,呈椭圆形或不规则形软组织肿块,突向肺野,边界较清楚.CT平扫示肿瘤密度较均匀12例,密度不均匀7例,15例肿瘤内伴有钙化.13例行增强检查,7例均匀强化,6例不均匀强化.8例MRI检查T1WI示肿瘤呈等或稍低信号,与胸壁肌肉相近,T2 WI呈不均匀稍高信号,3例肿瘤内伴出血、囊变呈混杂信号.结论 儿童患者,CT或MRI检查发现后纵隔肿物,特别是其内伴钙化者,诊断时应首先考虑神经母细胞瘤.  相似文献   

3.
目的 探讨卵巢纤维瘤的CT平扫及增强扫描的特征性表现.方法 回顾性分析经手术病理证实的20例卵巢纤维瘤患者临床及CT影像资料.所有病例均行盆腔CT平扫,其中13例行CT增强扫描,12例同时行上腹CT扫描.结果 本组20例卵巢纤维瘤中单侧发病19例,双侧发病1例.肿块呈类圆形或分叶状,边界清楚.最大径4.0~20.2 cm,平均9.5 cm.肿块密度不均匀16例,5例密度均匀.5例肿块伴钙化.1例伴蒂扭转.2例伴梅格氏综合征.增强CT扫描肿块呈轻度延迟强化,动脉晚期CT增强值为0.8~8.5 HU,平衡期CT增强值为3.9~27.6 HU.结论卵巢纤维瘤的CT表现具有一定特征性,CT增强扫描有助于提高诊断准确率.  相似文献   

4.
【摘要】 目的:探讨儿童骨肌来源外周性原始神经外胚层肿瘤(pPNETs)的CT和MRI影像学特点。方法:回顾性分析经我院病理证实的14例骨肌来源pPNETs患儿的CT及MRI影像学表现。其中男8例,女6例;年龄21个月~13岁,中位年龄9岁。10例行CT扫描,其中5例行CT增强扫描;6例行MRI检查,其中5例同时行MRI增强扫描。结果:本组14例中骨来源和软组织来源各7例,位于胸壁4例、肩胛骨、下肢、脊柱旁区和头部各2例、骨盆1例。骨来源pPNETs的CT表现为溶骨性为主的骨质破坏伴有周围软组织肿块,直径3~8cm,边界多模糊不清,增强后呈不均匀强化;主要MRI表现为T1WI上受累骨结构内见稍低信号,T2WI上呈高信号,骨皮质低信号不连续,周围可见囊实性肿块、呈明显不均匀强化。软组织来源的pPNETs CT表现为软组织密度肿块,内部可有低密度坏死区、钙化少见,肿块通常较大,直径5~15cm,增强扫描肿瘤内可见片絮状强化或不均匀轻度强化,邻近骨性结构可受累;主要MRI表现为T1WI上骨质破坏区多呈等信号或稍低信号,T2WI上多呈不均匀等信号及高信号,增强扫描呈不均匀明显强化,其内囊变坏死区无明显强化,周围骨性结构受累时呈略长T1、长T2信号。结论:儿童骨肌来源pPNET的影像学表现特异性不强,但在临床诊断儿童骨骼肌肉来源的恶性肿瘤时需要注意与本病进行鉴别诊断,CT和MRI不仅可以显示肿瘤的范围,同时对肿瘤可切除性的判断以及治疗效果的监测也很有帮助。  相似文献   

5.
目的探讨颌面部少见巨大肿瘤的CT表现,以提高CT诊断的准确性。方法回顾性分析经本院手术病理证实的8例颌面部巨大肿瘤:其中造釉细胞瘤4例、腺样囊性癌2例、牙源性透明细胞癌1例、骨化性纤维瘤1例的CT表现。结果造釉细胞瘤CT平扫颌骨变形膨胀,病变最大径约28cm×25cm×18cm,15cm×9cm×7cm,内密度不均匀,见粗大骨嵴,呈多房样改变,周围结构受压,增强扫描呈不均匀强化;腺样囊性癌CT平扫颌骨骨质破坏,边界模糊不清,软组织肿块形成,其内密度不均匀,增强扫描显示不均匀强化;牙源性透明细胞癌CT平扫显示颌骨骨质破坏,部分层面界限不清并侵犯颅底,其内密度不均匀,内有散在不规则的高密度骨组织影,增强扫描显示明显不均匀强化;骨化性纤维瘤CT平扫颌骨骨质膨胀破坏,范围较大,增强扫描强化较均匀。病变的最小径超过5cm。结论颌面部少见巨大肿瘤CT表现特点各不同,详细观察各自特点及发病部位可以较为正确的诊断。  相似文献   

6.
目的:分析眼附属器淋巴瘤的CT和MRI表现,提高对本病的影像学认识.方法:回顾性分析经手术或活检病理证实的55例(共64眼)眼附属器淋巴瘤的影像学表现,其中左眼27例,右眼19例,双眼9例.49例行CT扫描,3例行CT和MRI扫描,3例行MRI扫描.结果:肿块常侵犯多处部位,26例有眼睑或结膜侵犯,20例有泪腺侵犯,8例有肌锥内侵犯,16例有肌锥外侵犯,14例同时有肌锥内、外侵犯.34例肿块呈弥漫型,11例呈结节团块型,10例呈弥漫和结节混合型.眶内肿块常沿眶隔结构塑形生长,可环绕球壁、眼外肌、视神经生长.38例行平扫,显示淋巴瘤均呈中等密度,36例密度较均匀,2例密度欠均匀,边界模糊或欠清.40例行增强扫描,34例强化均匀,6例强化欠均匀,其中1例有液化表现,仅3例有骨质改变.MRI T1WI和T2WI上肿瘤信号较均匀,增强扫描示肿块均匀强化,3例采用脂肪抑制技术,肿块信号显示更清晰,边界更清楚.结论:眼附属器淋巴瘤的影像学表现有一定特征性,MRI脂肪抑制技术有助于了解肿瘤范围.  相似文献   

7.
目的:分析儿童肌纤维瘤的影像学表现,提高对此病的诊断水平。方法:回顾性分析本院2010年1月-2020年5月经手术病理证实的16例肌纤维瘤患儿的病例资料。12例行CT平扫,其中9例行CT增强扫描,5例行MRI平扫,其中4例行MRI增强扫描。观察分析肌纤维瘤的部位、数目、大小、形态、边界、有无骨侵犯、密度/信号和强化方式等征象。结果:16例共检出32个病灶,其中2例为多发病灶(分别有6和12个)。发病部位:头颈部6例,四肢5例,躯干2例,骨内2例(其中1例为多发),1例累及四肢、躯干等多部位;孤立性肿块14例,多中心性病变2例;9例呈类圆形,7例呈不规则形;5例边界清晰,11例边界模糊;2例骨质受侵犯。8例CT平扫呈低或稍低密度,1例呈稍高密度,3例呈混杂密度;CT增强扫描显示5例呈轻度不均匀强化,4例呈明显不均匀强化。MRI平扫T1WI上3例呈等~低信号,2例呈等~稍高信号;T2WI上4例呈高~低混杂信号,1例呈稍高信号;4例MRI增强呈明显不均匀强化。随访中有2例复发。结论:儿童肌纤维瘤是一种罕见的软组织肿瘤,其CT及MRI表现具有一定的特征性。  相似文献   

8.
目的 探讨异位妊娠的CT与MRI表现.方法 回顾性分析20例经手术证实的异位妊娠患者CT与MRI影像,其中输卵管妊娠11例,卵巢妊娠2例,宫角妊娠1例,切口妊娠6例;12例行CT检查,8例行MRI检查.结果 异位妊娠CT与MRI表现为子宫内膜以外部位的厚壁囊性、出血性或混杂密度/信号肿块,血管丰富,增强扫描厚壁环形强化、边缘明显强化或不均匀强化,伴不同程度的腹盆腔积血.输卵管或妊娠囊壁不完整,肿块境界不清、密度/信号不均匀伴中等度到大量腹盆腔积血,急性期出血或活动性出血提示异位妊娠破裂.结论 异位妊娠的CT与MRI表现具有一定的特征性,当育龄期女性出现腹盆腔出血或盆腔肿块时应考虑异位妊娠的可能性.  相似文献   

9.
卵巢硬化性间质瘤CT诊断   总被引:2,自引:0,他引:2       下载免费PDF全文
张伟强  陈英  朱翔  王立章  方春   《放射学实践》2009,24(7):767-769
目的:探讨卵巢硬化性间质瘤(SST)的CT表现.方法:回顾性分析3例经手术病理证实的卵巢硬化性间质瘤CT表现.结果:3例均为单发,肿瘤呈实性2例,囊实性1例.平扫肿块密度不均,动态增强扫描肿块边缘部分早期明显强化,延迟扫描呈持续性显著强化,2例实性肿块轻度向心性延迟强化,1例囊变区无强化.结论:SST动态增强扫描具有特征性强化表现,CT可提示本病的诊断.  相似文献   

10.
目的:探讨胃间质瘤的CT和MRI的表现,以提高诊断正确率。材料和方法:回顾性分析13例经病理学及免疫组化证实的胃间质细胞瘤患者的临床资料和CT、MRI表现。13例均行CT平扫和增强扫描,其中4例行MRI平扫和增强扫描。结果:肿瘤均为单发,腔内型3例,腔外型6例,哑铃型4例,圆形或类圆形9例,分叶形4例,直径3.0~10.4cm,平均7.5cm。CT平扫示肿瘤呈均匀等密度3例,肿块周边呈等密度,中间呈略低密度或低密度9例,呈高、低、等混杂密度1例。增强扫描示3例呈中度明显增强,10例中度不均匀增强,以静脉期明显。MRI平扫示1例肿块信号均匀,3例肿块信号不均匀,增强扫描肿块信号均匀或不均匀增强。病理检查10例恶性,3例良性。结论:胃间质瘤CT、MRI具有一定的特征性表现,对诊断有一定的价值,但不能定性,确诊需要依靠电镜检查和免疫组化。  相似文献   

11.
目的:分析肾少见良性肿瘤的影像学表现,提高术前诊断准确性。方法:回顾性分析20例肾脏少见良性肿瘤的影像学资料,其中嗜酸细胞腺瘤9例、后肾腺瘤1例、不典型血管平滑肌脂肪瘤(AML)4例(上皮样型2例,平滑肌瘤型2例)、纤维瘤3例、中胚叶肾瘤2例、神经鞘瘤1例。15例行CT检查,3例行MRI检查,2例同时进行了CT和MRI检查。结果:本组病例除1例中胚叶肾瘤和1例神经鞘瘤外,均表现为境界清楚、均质性的实性肿块影。中央瘢痕及可以高于肾皮质的强化方式是嗜酸细胞腺瘤的特征。不典型AML、纤维瘤、后肾腺瘤及实性中胚叶肾瘤,在抑脂序列T2WI上呈较明显的低信号,且纤维瘤和后肾腺瘤都具有延迟强化的特征。良性神经鞘瘤具有境界清楚和易于发生坏死、囊变的特征。囊性中胚叶肾瘤缺少特征性的影像学表现。结论:肾少见良性肿瘤的影像学表现具有一定的特征性,有助于与肾癌进行鉴别,准确的术前诊断对指导治疗具有重要价值。  相似文献   

12.
OBJECTIVE: The initial and follow-up CT and MRI images of ten patients with hepatic metastases from ovarian tumors were retrospectively analyzed to establish their features and sequential changes in appearance. MATERIALS AND METHODS: Ten patients with hepatic metastasis from ovarian tumors received initial and follow-up CT and MRI examinations. Six patients were followed up every two to three weeks before surgical tumor resection. Both CT and MR images were analyzed by two radiologists. RESULTS: A total of fourteen lesions were detected by CT and MRI in 10 patients. All 14 lesions were demonstrated as areas of marked hyperintensity on T2-weighted MRI. Eleven cyst-like tumors were demonstrated as round or oval low density lesions on CT and as areas of hypointensity on T1-weighted imaging. Three lesions were shown as solid masses with slightly low attenuation at the initial CT examination and slightly low or iso-intensity areas on T1-weighted imaging, and these lesions showed early peripheral globular enhancement and delayed enhancement on contrast-enhanced CT and MR imaging. Cystic formation was observed two to three weeks later after initial study in all the 3 solid lesions. Rapid subcapsular effusion, which showed obvious enhancement on delayed Gd-DTPA enhanced MR imaging, was observed in two patients. CONCLUSION: The hepatic metastatic tumor from cystic ovarian carcinoma may manifest as a well-defined cystic lesion or as a solid mass, and the solid mass shows delayed enhancement on contrast-enhanced CT and MR imaging. Furthermore, rapid cystic formation and rapid subcapsular extension is frequently seen.  相似文献   

13.
目的探讨卵巢印泡膜一纤维瘤的CT及磁共振成像(MRI)表现特点,与病理结果进行对照,以提高对卵泡膜一纤维瘤影像表现的认识。方法回顾分析经手术病理证实的26例卵泡膜一纤维瘤患者的临床和影像资料。结果26例患者中行cT检查22例,MRI检查9例,均查者5例。其中1例患者双侧发生,27个肿瘤均呈阋形或分叶状,其中实性肿块18例.囊实性肿块9例。肿块边界均较清楚。其中13例伴有少量盐腔积液,2例伴子宫内膜增生。盆腔均未见肿大淋巴结。CT平扫显示实性肿瘤和囊实性肿瘤的实性部分的密度较子宫肌层相仿,增强后轻度强化或无强化:MRI显示病灶T1WI均呈等低信号,1例病灶T2WI呈稍高信号,8例T2WI呈低信号。镜下见肿瘤细胞呈短梭形,细胞质内含有大量脂肪小滴,细胞核未见明显核分裂。细胞呈漩涡状、束状排列,周丽被大量纤维组织分隔。结论卵巢卵泡膜.纤维瘤的影像表现具有一定的特征,对该病的术前正确诊断具有重要意义  相似文献   

14.
纵隔囊性病变的CT与MRI诊断   总被引:3,自引:0,他引:3       下载免费PDF全文
目的:探讨纵隔囊性病变的CT、MRI诊断及鉴别诊断。方法:回顾性总结30例经手术、病理确诊的纵隔囊性病变的CT及MRI表现,包括胸腺囊肿7例,囊性畸胎瘤8例,气管、支气管囊肿9例,食管囊肿4例,囊性淋巴管瘤2例。结果:不同纵隔囊性病变均有其较特定的发病部位。7例胸腺囊肿中6例位于前上纵隔的胸腺区,1例位于前纵隔中下部;8例囊性畸胎瘤主要位于前纵隔中部、大血管起始处;9例气管、支气管囊肿位于中上纵隔,气管、支气管右旁区;4例食管囊肿,其中3例位于后纵隔,1例位于中纵隔;2例囊性淋巴管瘤,其中1例为颈纵隔型,1例为颈一腋纵隔型。结论:纵隔囊性病变虽无明显特征性影像学表现,仔细观察CT与MRI征象特点,结合发病部位,对提高本病的诊断具有重要意义。  相似文献   

15.
眼球脉络膜血管瘤的影像学表现   总被引:16,自引:10,他引:6  
目的:探讨眼球脉络膜血管瘤的CT、MRI表现及其诊断、鉴别诊断价值。方法:回顾性分析9例经病理(3例)和临床证实(6例)的脉络膜血管瘤。CT扫描6例,MR检查4例,9例均行B超检查,3例作了眼底荧光血管造影。结果:2例CT平扫示眼球后极球壁轻度或新月形增厚,与球壁呈等密度,5例(1例平扫+增强)增强示眼球后极部高密度梭形或扁平状隆起均匀肿块,瘤体强化明显。与玻璃体比较3例MR T1WI呈高信号,T2WI呈低信号,与视神经、眼外肌相比呈等信号;1例较小肿瘤辅以增强T1WI脂肪抑制技术被清楚显示。渗出性视网膜脱离在T1WI、T2WI上均呈中、高信号;增强T1WI瘤体显著强化,边界清晰,且信号均匀。B超检查8例为实质不均质肿块占位,1例为均质肿块占位,9例均探及视网膜脱离光带。结论:CT+MRI+B超检查对脉络膜血管瘤可得到较为全面的影像学诊断资料,MRI在该病的诊断及鉴别诊断中较CT及B超更具敏感性和特异性。  相似文献   

16.
目的:分析颅底骨源性良性及瘤样病变的MRI表现并与CT和病理对照研究。方法:搜集经手术病理证实的颅底骨源性良性肿瘤及瘤样病变21例(骨巨细胞瘤2例,软骨黏液性纤维瘤4例,骨化性纤维瘤3例,骨瘤3例,骨纤维异常增殖症9例),全部行MRI检查(14例增强检查),7例CT检查。结果:绝大多数病变均有清晰的边界,T1WI呈低或等信号,T2WI高或混杂信号,增强后呈周边及不均匀强化。MR对钙化和骨质破坏的显示不如CT敏感。结论:MRI对颅底骨源性良性肿瘤及瘤样病变的诊断具有一定的价值,尤其能够进行精确的定位诊断。  相似文献   

17.
OBJECTIVE: We describe the imaging findings of malignant mixed müllerian tumor (MMMT) of the ovary, which have not previously been reported. MATERIALS AND METHODS: We experienced 13 cases of ovarian MMMT in eight patients. All patients underwent surgical resection and the MMMTs were confirmed pathologically. US (n = 8), CT (n = 8), and MRI (n = 1) examinations were performed before operation. Imaging features were analyzed retrospectively for bilaterality, tumor solidity (cystic or solid), size, and contrast enhancement of the tumor on CT and MRI. Presence of ascites and other evidence of peritoneal seeding, adjacent organ invasion, distant metastasis, and surgical staging were also evaluated. RESULTS: There were bilateral ovarian MMMTs in five patients and unilateral MMMTs in three patients. Two of the MMMTs were multiseptated cystic, and 11 were mixed (solid and cystic). The diameter of the largest dimension was less than 5 cm in one case, 5-10 cm in two cases, and larger than 10 cm in 10 cases. Dense homogeneous contrast enhancement of the solid component was seen in 11 mixed masses. Ascites were found in all patients. Other evidence of peritoneal seeding and direct invasion into adjacent organ such as the uterus or sigmoid colon was seen in five patients each. Pleural metastasis was present in one patient. Surgical stages were FIGO classification IIIb and IV in one patient each, and IIIc in six patients. CONCLUSION: Ovarian MMMTs usually present as aggressive, bilateral, large, solid and cystic tumors, combined with ascites, frequent peritoneal seeding, and adjacent organ invasion.  相似文献   

18.
眼部淋巴瘤CT和MRI诊断   总被引:1,自引:0,他引:1  
目的:分析眼部恶性淋巴瘤的CT和MRI表现特点,探讨二者诊断淋巴瘤的价值。方法:13例眼部淋巴瘤,CT检查12例,MRI检查5例。结果:所有病例经病理证实,其中10例为单侧,3例为双侧,均累及隔前眶周组织,8例以眼眶的上象限为主,5例以下象限为主,境界不清。5例呈局限性块影;8例呈弥漫软组织影,沿肌锥外向眶内浸润生长,同时累及泪腺和邻近眼外肌,并沿肌锥外向眶内生长呈铸形样改变;3例大部分眼环被肿瘤组织环绕,呈光芒样改变,并累及球后。CT平扫肿瘤组织呈境界欠清的中等密度软组织块影,MRI呈较低或略高信号强度,增强扫描肿块均呈较明显的均匀强化。结论:眼部恶性淋巴瘤的CT和MRI表现具有一些特征,影像学检查对本病的诊断具有重要价值。  相似文献   

19.
卵巢囊性病变的CT诊断   总被引:28,自引:2,他引:26  
目的 提高CT诊断卵巢囊性病变的正确性。材料与方法 搜集经手术和病理证实的121例共161个卵巢区囊性病变,对其CT表现作回顾性分析。结果 161个病灶中,良性102例134个病灶,恶性19例27个病灶,120个为完全囊性,41个有囊壁结节或实性部分,分别占74.5%和25.5%,其中囊性畸胎瘤21例25个病灶,囊腺瘤18例,均为单个病灶,囊腺癌7例12个病灶,Krukenberg瘤5例7个病灶,内膜异位囊肿31例39个病灶,黄体囊肿8例9个病灶,滤泡囊肿8例9个病灶,浆液或粘液性囊肿11例,中肾管囊肿10例,陈旧性异位妊娠4例,卵巢输卵管脓肿,炎症积水9例13个病灶,其他4例,术前CT诊断准确庞81.8%。结论 卵巢囊性病变种类较多,基本CT表现多类似,但良性病变常为圆形或卵圆形,囊壁薄而规则;恶性病变多为双侧不规则形,囊壁及囊内分隔厚而不规则,结节状,CT在卵巢囊性病变的诊断中有较高价值。  相似文献   

20.
AIM: To record the clinical findings and magnetic resonance imaging (MRI) characteristics of intracranial gangliogliomas in 16 patients. MATERIALS AND METHODS: Sixteen patients were imaged using unenhanced and contrast-enhanced MRI. Eight patients underwent unenhanced CT and of these, three underwent contrast-enhanced CT. Two radiologists read the images retrospectively. The images were studied with regard to location, size, margin, signal intensity, enhancement characteristics, cystic changes, and presence of calcifications. Clinical data, such as presenting signs and symptoms, physical findings, and medical histories, were collected. Histopathological and immunohistochemical studies were performed and analysed by two pathologists. RESULTS: In 12 cases the tumours were located in one of the cerebral hemispheres; in the other cases they were located in the brainstem, cerebellum, suprasellar area or the thalamus. The tumour dimension varied from 1-7 cm, with a mean of 3.6 cm+/-1.8 cm. The MRI features of ganglioglioma in the present cohort can be divided into three patterns: cystic (n=2), cystic-solid (n=6), and solid (n=8). Solid lesions had a predilection for the temporal lobe; cystic and cystic-solid tumours had a wide anatomical distribution. Cystic lesions were significantly smaller than both cystic-solid and solid lesions (F=4.28, P<0.05). Cystic changes in the cystic-solid tumours showed one of the following patterns: those with walls showing contrast enhancement, those containing an enhancing nodule, or cysts without an obvious wall. The solid portion of cystic-solid gangliogliomas and the entire tumour in solid tumours showed homogeneous enhancement of variable degrees on T1-weighted (T1W) spin-echo (SE) images. Five tumours had mild or moderate oedema. In one patient two separate gangliogliomas were found, each lesion exhibiting different MRI features: solid and cystic-solid. One case of cortical ganglioglioma was found, causing bone erosion due to pressure. One tumour with chronic haemorrhage was found in the study. CONCLUSION: MRI features of gangliogliomas are non-specific. A ganglioglioma should be suspected when a tumour shows the following features: (1) a solid lesion located in the temporal lobes with mild or no oedema and homogeneous enhancement on SE T1W images; or (2) a small cystic lesion or cystic-solid mixed mass with a wall enhancement or a markedly enhanced nodule. We report a patient with two separate gangliogliomas and a case with bone erosion.  相似文献   

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