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三例多脾综合征患者的CT、MRI表现 被引量:15

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摘要 多脾综合征(polysplenia syndrome)是一种少见的先天性多系统畸形组成的综合征,主要为多脾、心血管及其他内脏发育异常的联合畸形。以往多在尸检或手术时发现.现在由影像检查发现的报道逐渐增多。
出处 《中华放射学杂志》 CAS CSCD 北大核心 2011年第4期403-405,共3页 Chinese Journal of Radiology
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参考文献6

  • 1Peoples WM,Moller JH,Edwards JE.polysplenia:a review of 146.Pediatr Cardiol,1983,4:129-137.
  • 2陈虎 杨德琪.多脾综合征1例[J].中华放射学杂志,1996,30(7):503-504.
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二级参考文献5

共引文献7

同被引文献54

  • 1邓生德,谭兴,郑生喜,魏铭,吴惠宁,刘伯儒,燕小梅.多脾综合征合并右室双出口一例[J].中华放射学杂志,2005,39(11):1224-1225. 被引量:5
  • 2孙爱敏,朱铭,钟玉敏,王谦.磁共振成像在心房异构诊断中的应用[J].中国临床医学影像杂志,2007,18(7):485-487. 被引量:3
  • 3白凯,苏肇伉,郭颖,朱敏.功能性单心室全腔肺吻合术后运动功能评价[J].临床儿科杂志,2007,25(8):708-710. 被引量:1
  • 4Gayer G, Apter S, Jonas T, et al. Polysplenia syndrome detected in adulthood: report of" eight cases and review of the literature. Abdom Imaging, 1999, 2d(2) : 178-184.
  • 5Miyaji K, Nagata N, Matsui H, et al. Successful fontan proce- dure for asplenia with pulmonmy atresia and major aortopulmo- nary collateral arteries [J]. J Thorac Cardiovasc Surg, 2003, 126(5): 1648-1650.
  • 6Takeuchi K, Murakami A, Hirata Y, et al. Surgical outcome of heterotaxy syndrome in a single institution [J]. Asian Cardio- vasc Thorac Ann, 2006, 14: 489-494.
  • 7Aeba R, Katogi S, Hashizume K, et al. Individualized total ca- vopulmonary connection technique for patients with asplenia syndrome[J]. Ann Thorac Surg, 2002, 73(4) : 1274-1280.
  • 8Karadeniz A, Semiz OA, Sahin S. Polysplenia/Heterotaxy syn- drome associated with aortic coarctation and multiple venous anomalies: muhidetector computed tomography findings [J]. Vasc Endovascular Surg, 2010, 44(5): 381-384.
  • 9Bartram U, Wirbelauer J, Speer CP. Heterotaxy syndrome-as- plenia and polysplenia as indicators of visceral malposition and complex congenital heart disease [J]. Biol Neonate, 2005, 88(4): 278-290.
  • 10Kwon SH, Oh JH, Han MY. Polysplenia and interrupted infe- rior vena cava with azygos continuation: 64-Slice multidetec- tor row computed tomography findings [J]. Pediatr Cardiol, 2010, 31(6) : 927-928.

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