蚌埠医学院学报
蚌埠醫學院學報
방부의학원학보
ACTA ACADEMIAE MEDICINAE BENGBU
2014年
10期
1401-1405,1406
,共6页
张应战%张禹%秦添%王星星%徐茂林%冯雨婷%邓雪飞
張應戰%張禹%秦添%王星星%徐茂林%馮雨婷%鄧雪飛
장응전%장우%진첨%왕성성%서무림%풍우정%산설비
脑肿瘤%星形细胞瘤%磁共振成像
腦腫瘤%星形細胞瘤%磁共振成像
뇌종류%성형세포류%자공진성상
brain neoplasms%astrocytoma%magnetic resonance imaging
目的:提高对脑多形性黄色星形细胞瘤( PXA)临床、病理及MRI特征的认识。方法:回顾性分析8例PXA的MRI表现并复习相关文献,8例脑PXA均经病理证实,均行MRI平扫、增强扫描及扩散加权成像,2例行多体素磁共振波谱( TE135ms)和灌注加权成像检查。结果:8例PXA年龄14~56岁,25岁以下者6例。伴间变特征者2例。7例单发,1例伴间变特征者为单发肿块伴周围子灶。5例发生或累及颞叶,6例位于皮层及皮层下。 MRI表现5例呈囊实性,3例呈实性,1例伴局部软脑膜受侵,1例伴出血及室管膜受侵(伴间变特征),1例伴侧脑室播散(伴间变特征)。肿瘤实性区均呈明显强化的稍长T1稍长T2信号,扩散加权成像呈等或稍高信号,表观扩散系数值与正常皮层下脑白质差异无统计学意义(P>0.05)。2例囊实性者囊壁强化。所有肿瘤周围均有轻到中度水肿。2例肿瘤实性区呈高灌注,胆碱峰明显升高,N-乙酰天门冬氨酸峰明显下降,多见乳酸峰。结论:PXA好发于青少年,多发生于幕上脑浅部,多位于颞叶,其病理学及遗传学特征有别于其他星形细胞瘤,肿瘤全切是预后的主要保证。 PXA的常规MRI、磁共振灌注加权成像和磁共振波谱具有一定特点。
目的:提高對腦多形性黃色星形細胞瘤( PXA)臨床、病理及MRI特徵的認識。方法:迴顧性分析8例PXA的MRI錶現併複習相關文獻,8例腦PXA均經病理證實,均行MRI平掃、增彊掃描及擴散加權成像,2例行多體素磁共振波譜( TE135ms)和灌註加權成像檢查。結果:8例PXA年齡14~56歲,25歲以下者6例。伴間變特徵者2例。7例單髮,1例伴間變特徵者為單髮腫塊伴週圍子竈。5例髮生或纍及顳葉,6例位于皮層及皮層下。 MRI錶現5例呈囊實性,3例呈實性,1例伴跼部軟腦膜受侵,1例伴齣血及室管膜受侵(伴間變特徵),1例伴側腦室播散(伴間變特徵)。腫瘤實性區均呈明顯彊化的稍長T1稍長T2信號,擴散加權成像呈等或稍高信號,錶觀擴散繫數值與正常皮層下腦白質差異無統計學意義(P>0.05)。2例囊實性者囊壁彊化。所有腫瘤週圍均有輕到中度水腫。2例腫瘤實性區呈高灌註,膽堿峰明顯升高,N-乙酰天門鼕氨痠峰明顯下降,多見乳痠峰。結論:PXA好髮于青少年,多髮生于幕上腦淺部,多位于顳葉,其病理學及遺傳學特徵有彆于其他星形細胞瘤,腫瘤全切是預後的主要保證。 PXA的常規MRI、磁共振灌註加權成像和磁共振波譜具有一定特點。
목적:제고대뇌다형성황색성형세포류( PXA)림상、병리급MRI특정적인식。방법:회고성분석8례PXA적MRI표현병복습상관문헌,8례뇌PXA균경병리증실,균행MRI평소、증강소묘급확산가권성상,2례행다체소자공진파보( TE135ms)화관주가권성상검사。결과:8례PXA년령14~56세,25세이하자6례。반간변특정자2례。7례단발,1례반간변특정자위단발종괴반주위자조。5례발생혹루급섭협,6례위우피층급피층하。 MRI표현5례정낭실성,3례정실성,1례반국부연뇌막수침,1례반출혈급실관막수침(반간변특정),1례반측뇌실파산(반간변특정)。종류실성구균정명현강화적초장T1초장T2신호,확산가권성상정등혹초고신호,표관확산계수치여정상피층하뇌백질차이무통계학의의(P>0.05)。2례낭실성자낭벽강화。소유종류주위균유경도중도수종。2례종류실성구정고관주,담감봉명현승고,N-을선천문동안산봉명현하강,다견유산봉。결론:PXA호발우청소년,다발생우막상뇌천부,다위우섭협,기병이학급유전학특정유별우기타성형세포류,종류전절시예후적주요보증。 PXA적상규MRI、자공진관주가권성상화자공진파보구유일정특점。
Objective:To analyze the MRI features of brain pleomorphic xanthoastrocytomas ( PXA ) in 8 cases for improving its clinical,pathological and MRI features understanding. Methods:The MRI plain scans, enhanced scans and DWI were explored in 8 cases with brain PXA diagnosed by pathology,and the MRS combined with PWI were examined in 2 cases. Results:Three patients were male and 5 patients were female,the age of all patients ranged from 14 to 56 years old(including 6 patients less than 25 years old). Interstitial change in 2 cases were found. Single lesion in 7 cases and single lesion complicated with round multiple lesions in 1 case with interstitial change were found. Five cases located or involved in temporal lobe,6 cases located in the cortex and subcortical region. Solid-cystic tumors in 5 cases and solid tumors in 3 cases( including 1 case with partial pia mater invasion,1 case with bleeding and ependymal invasion and 1 case with lateral ventricle spread) were identified by MRI. The tumor solid area showed slightly hypointense on T1-weighted images, slightly hyperintense on T2-weighted images and marked enhancement. The difference between the apparent diffusion coefficient value and subcortex alba was not statistical significance(P>0. 05). The solid-cystic capsule wall enhanced in 2 cases. The light to moderate degree edema around the tumor were detected in all tumors. The significant increasing Cho peak and decreasing N-acetyl aspartic acid peak and Lip peak were found in tumor solid area with high perfusion. Conclusions:PXA occurres usually in adolescent,which locates the brain shallow position of the temporal lobe. The tumor pathologic and genetic characteristics are different from other astrocytomas, complete surgical excision is important for a good prognosis. The conventional magnetic resonance imaging,magnetic resonance perfusion weighted imaging and magnetic resonance spectroscopy of PXA have certain characteristics.