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产前超声诊断胎儿神经母细胞瘤的临床研究 被引量:2

Clinical Study of ultrasound diagnosis on neuroblastoma in fetus
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摘要 目的探讨胎儿神经母细胞瘤(neuroblastoma,NB)的超声表现及其超声诊断的价值。方法根据成都市妇女儿童中心医院超声科2009年2月至2013年10月产前超声检出的8例胎儿NB及其出生后手术及病理证实,回顾性分析胎儿各个时期的产前超声图像。结果 8例胎儿中,肿瘤位于胸腔/纵隔4例,来源于肾上腺者4例;8例产前均做出正确诊断,胎儿出生后,均由CT、MRI及产后超声证实,手术病例7例,术前超声诊断符合率100%。结论超声可以诊断胎儿NB,为临床早期干预提供依据。 Objective To explore the ultrasound feature of neuroblastoma( NB) in fetus and the diagnosis value of ultrasound.Methods According to prenatal ultrasonography and postoperative pathological diagnosis,8 cases of NB in fetus in Women and Children's Central Hospital of Chengdu City from February 2009 to October 2013 were selected,a retrospective analysis of ultrasound images of fetus in different periods were made. Results 4 cases that the tumor were located in chest / mediastinum,4 cases in adrenal gland. All cases were diagnosed correctly through prenatal ultrasound and the diagnosis were proved to be correctly through CT and MRI after birth. 7 cases resorted to surgery afterwards,the postoperative ultrasound diagnosis was 100% correctly. Conclusion NB in fetus can be diagnosed by ultrasound,which can provide basis for early clinical intervention.
出处 《中国计划生育和妇产科》 2014年第8期37-38,44,共3页 Chinese Journal of Family Planning & Gynecotokology
关键词 胎儿神经母细胞瘤 超声诊断 neuroblastoma in fetus ultrasound diagnosis
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  • 1Hann HW, Evans AE, Siegel SE, et al. Prognostic importance of serum ferritin in patients with stages Ⅲ and IV neuroblastoma:The Children's Cancer Study Group experience [ J ]. Cancer Res, 1985,45 ( 6 ) : 2843 - 2848.
  • 2Shuster J J, McWilliams NB, Castleberry R ,et al. Serum lactate dehydrogenase in childhood neuroblastoma. A Pediatric Oncology Group recursive partitioning study [ J ]. Am J Clin Oncol, 1992,15 ( 4 ) : 295 - 303.
  • 3de Bernardi B, Pianca C, Boni L, et al. Disseminated neuroblastoma (stage IV and IV -S) in the first year of life. Outcome related to age and stage. Italian Cooperative Group on Neuroblastoma [ J ]. Cancer, 1992,70(6) : 1625 - 1633.
  • 4Lastowska M, Cullinane C, Variend S, et al. United Kingdom Children Cancer Study Group and the United Kingdom Cancer Cytogenetics Group: Comprehensive genetic and histopathologic study reveals three types of neuroblastoma tumors [ J ]. J Clin Oncol,2001 , 19 ( 12 ) : 3080 - 3090.
  • 5Shimada H,Ambros IM,Dehner LP,et al. The international neuroblastoma pathology classification (the Shimada system) [ J]. Cancer, 1999, 86(2) :364 -372.
  • 6Goto S, Umehara S, Gerbing RB,et al. Histopathology( international neuroblastoma pathology classification) and MYCN status in patients with peripheral neuroblastic tumors: A report from the Children's Cancer Group [ J ]. Cancer,2001,92 ( 10 ) :2699 - 2708.
  • 7Kubota M, Suita S,Tajiri T,et al. Analysis of the prognostic factors relating to better clinical outcome in ganglioneuroblastoma[ J ]. J Pediatr Surg,2000,35 ( 1 ) :92 - 95.
  • 8Matthay KK, Castleberry RP. Treatment of advanced neuroblastoma: The US experience [ M ]//Brodeur GM, Sawada T, Tsuchida Y, et al. Neuroblastoma. Amsterdam : Elsevier Science,2000:417 - 436.
  • 9Kushner BH,LaQuaglia MP, Bonilla MA,et al. Highly effective induction therapy for stage 4 neuroblastoma in children over 1 year of age [ J]. J Clin Oncol, 1994,12( 12 ) :2607 - 2613.
  • 10Nitschke R, Parkhurst J, Sullivan J, et al. Topotecan in pediatric patients with recurrent and progressive solid tumors:A Pediatric Oncology Group phase Ⅱ study[J]. J Pediatr Hematol Oncol, 1998,20(4) :315 - 318.

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  • 1Moon SB. Shin HB. Seo JM, et a!. Clinical features and surgical outcome of a suprarenal mass detected before birth [J] . Pedialr Surg Int, 2010, 26(3): 241-246. DOl: 10. 1007/s00383-009-2531- 7.
  • 2Balassy C, Navarro OM, Daneman A. Adrenal masses in children [J]. Radiol Clin North Am, 2011, 49( 4) : 711-727. DOl: 10.1016/j. rcl. 2011.05.001.
  • 3Nowak D. Goralczyk K, Zurada A, et al , Morphometrical analysis of the human suprarenal gland between the 4th and 7th months of gestation[J] . Ann Anat, 2007,189(6) : 575-582.
  • 4Schrauder MG, Hammersen G, Siemer J, et al , Fetal adrenal haemorrhage two-dimensional and three-dimensional imaging [J] .Fetal Diagn Ther, 2008, 23( 1) : 72-75.
  • 5Stimac G, Katusic J, Sucic M, et al. A giant hemorrhagic adrenal pseudocyst: case report [J] . Med Prine Pract, 2008, 17 ( 5 ) : 419- 421. DOl: 10.1159/000141509 .
  • 6Moon SB,Shin HB,Seo JM,et al.Clinical features and surgical outcome of a suprarenal mass detected before birth.Pediatr Surg Int,2010,26(3):241-246.
  • 7Balassy C,Navarro OM,Daneman A.Adrenal masses in children.Radiol Clin North Am,2011,49(4):711-727,vi.
  • 8Nowak D,Góralczyk K,Zurada A,et al.Morphometrical analysis of the human suprarenal gland between the 4th and 7th months of gestation.Ann Anat,2007,189(6):575-582.
  • 9Schrauder MG,Hammersen G,Siemer J,et al.Fetal adrenal haemorrhage-two-dimensional and three-dimensional imaging.Fetal Diagn Ther,2008,23(1):72-75.
  • 10Hsieh CC,Chao AS,Hsu JJ,et al.Real-time and power Doppler imaging of fetal adrenal hemorrhage.Chang Gung Med J,2005,28(12):860-865.

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