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湖北省自然科学基金(2012FFB04422)

作品数:3 被引量:16H指数:2
相关作者:胡慧娟杨桂芳屈艳娟周素军袁玉峰更多>>
相关机构:武汉大学襄阳市中心医院武汉亚洲心脏病医院更多>>
发文基金:湖北省自然科学基金更多>>
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胸腺瘤术前CT分期与术后Masaoka临床分期相关性分析被引量:8
2013年
目的探讨胸腺瘤术前CT分期与术后Masaoka临床分期之间的相关性。方法回顾分析比较105例胸腺瘤患者术前CT特征、临床特点及术后Masaoka临床分期。结果病变CT分期与Masaoka临床分期有明显关系,包括病灶大小(P=0.028)、形态(P<0.001)、密度(P=0.002)、包膜完整性(P<0.001)以及周边组织受累情况(P<0.001)。通过CT发现34.78% MasaokaⅠ期病灶<5cm,而仅有8.70% MasaokaⅠ期病灶≥10cm;相反,仅有16.67%的MasaokaⅣ期病灶<5cm,而有37.50% MasaokaⅣ期病灶≥10cm。MasaokaⅠ期和Ⅱ期病灶多呈圆形或卵圆形、边界清楚、密度均匀;MasaokaⅢ期和Ⅳ期肿块形态不规则、密度不均匀、包膜不完整;Ⅲ期(80.00%)和Ⅳ期(87.50%)侵袭性肿块明显多于Ⅰ期(0%)和Ⅱ期(40.00%)。MasaokaⅠ期与CTⅠ期病灶的一致性明显高于其他分期(Kappa=0.884)。重症肌无力发生率在各Masaoka临床分期之间无差异。结论胸腺瘤术前CT分期与术后Masaoka临床分期一致性较高,有利于患者治疗方案的制订及对远期疗效的评估。
刘国兵屈艳娟胡慧娟周素军袁玉峰杨桂芳
关键词:胸腺瘤肿瘤分期重症肌无力
胸腺上皮肿瘤CT表现与WHO病理分型的相关性研究被引量:6
2013年
目的:探讨胸腺上皮肿瘤CT表现与WHO病理分型之间的关系。方法:对105例胸腺上皮肿瘤采用2004年WHO分类法进行病理分型。利用CT资料统计肿瘤大小、形状、钙化、坏死或囊变、包膜完整性、邻近组织侵犯、淋巴结肿大及有无胸水,对不同病理类型胸腺瘤的CT表现进行χ2检验或精确概率法检验,分析其CT表现间的差异性,以P<0.05为差异具有显著性。结果:105例中男性52例,女性53例;年龄18-75岁,平均(47.98±12.54)岁。不同病理类型胸腺肿瘤中大小、形状、坏死或囊变、包膜完整性、邻近组织侵犯、淋巴结肿大及有无胸水差异有显著性(P<0.05)。B2型、B3型及胸腺癌较其它型瘤体大,B3型胸腺瘤及胸腺癌超过50%瘤体大于10cm。A、AB及B1型多为圆形或类圆形,B3型胸腺瘤75%及胸腺癌85%瘤体不规则。B3型胸腺瘤及胸腺癌出现坏死或囊变分别为67%、57%。B3型胸腺瘤83%、胸腺癌100%包膜破坏。随着恶性程度增高瘤周组织侵犯率升高,B2型为33%、B3型为75%、胸腺癌为81%。B3型50%、胸腺癌48%出现胸水。钙化多见于B型胸腺瘤。结论:不同病理类型胸腺上皮肿瘤有不同的CT表现,CT表现能反映胸腺肿瘤病理特点。
屈艳娟陈鑫廖美焱胡慧娟周素军杨桂芳
关键词:胸腺胸腺上皮肿瘤胸腺癌病理
Diagnosis of Congenital Aortic Arch Anomalies in Chinese Children by Multi-Detector Computed Tomography Angiography被引量:2
2013年
Summary: The purpose of this study was to evaluate the value of multi-detector computed tomography (MDCT) angiography for the diagnosis of congenital aortic arch anomalies and present the radiological images of congenital aortic arch anomalies in Chinese children. MDCT angiography and transthoracic echocardiography (TTE) were applied for the diagnosis of congenital aortic arch anomalies in 362 Chi- nese children between May 2006 and December 2011 (age ranges from 5 days to 12 years; mean age, 3.3 years). Surgery and/or catheter angiography (CA) were conducted in all patients to confirm the final diagnosis. In the 362 Chinese children with congenital heart anomalies, congenital aortic arch anomalies were definitely diagnosed in 198 children and 164 children ruled out by operation and/or (CA). Among the 198 children with anomalies, coarctation of aorta (CoA), interruption of aortic arch (IAA), fight aor- tic arch, aberrant right subclavian artery and double aortic arch were diagnosed in 134, 32, 20, 10 and 2 children respectively, and there were 6 cases with uncommon congenital aortic arch anomalies: 2 had double aortic arch including 1 with five branches of the aortic arch, 2 had isolation of the right sub- clavian artery with two patent ductus arteriosus (PDA), 1 had an isolation of the common carotid artery with a PDA, and 1 had double PDA with a single ventricle and pulmonary artery atresia. Among the 32 children with IAA, 28 were of type A, and 4 were of type B. The diagnostic sensitivity, specificity and accuracy of MDCT angiography for congenital aortic arch anomaiies were 100% (198/198), 98% (161/164) and 99% (359/362), respectively. The diagnostic sensitivity, specificity and accuracy of TTE were 92% (182/198), 81% (133/164) and 87% (315/362), respectively. In conclusion, MDCT angiogra- phy is a reliable, noninvasive imaging technique for the diagnosis of congenital aortic arch anomalies in children. Sometimes, even more information can be obtaine
陈鑫屈艳娟彭志远鲁锦国马小静
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