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中华医学超声杂志(电子版) ›› 2021, Vol. 18 ›› Issue (05) : 451 -456. doi: 10.3877/cma.j.issn.1672-6448.2021.05.003

所属专题: 文献

妇产科超声影像学

胎儿期中胚层肾瘤超声特征及病理对照分析
王颖芳1, 杨小红1,(), 赵胜1, 刘思1, 杨帆1, 张晓燕1, 兰为顺2   
  1. 1. 430070 武汉,湖北省妇幼保健院超声科
    2. 430070 武汉,湖北省妇幼保健院医学影像科
  • 收稿日期:2019-10-31 出版日期:2021-05-01
  • 通信作者: 杨小红
  • 基金资助:
    湖北省卫生计生科研基金资助(WJ2018H0148)

Fetal mesoblastic nephroma: prenatal ultrasonographic features and pathological analysis

Yingfang Wang1, Xiaohong Yang1(), Sheng Zhao1, Si Liu1, Fan Yang1, Xiaoyang Zhang1, Weishun Lan2   

  1. 1. Department of Ultrasonography, Hubei Maternal and Child Health Hospital, Wuhan 430070, China
    2. Department of Medical Imaging, Hubei Maternal and Child Health Hospital, Wuhan 430070, China
  • Received:2019-10-31 Published:2021-05-01
  • Corresponding author: Xiaohong Yang
引用本文:

王颖芳, 杨小红, 赵胜, 刘思, 杨帆, 张晓燕, 兰为顺. 胎儿期中胚层肾瘤超声特征及病理对照分析[J/OL]. 中华医学超声杂志(电子版), 2021, 18(05): 451-456.

Yingfang Wang, Xiaohong Yang, Sheng Zhao, Si Liu, Fan Yang, Xiaoyang Zhang, Weishun Lan. Fetal mesoblastic nephroma: prenatal ultrasonographic features and pathological analysis[J/OL]. Chinese Journal of Medical Ultrasound (Electronic Edition), 2021, 18(05): 451-456.

目的

总结胎儿期中胚层肾瘤的超声表现并与病理组织学类型对照分析。

方法

对 2003 年 1 月至 2018 年 12 月湖北省妇幼保健院产前超声发现肾区肿块并经病理证实的 4例中胚层肾瘤胎儿的超声图像、磁共振影像特征、病理组织学类型及随访结果进行综合分析。

结果

4例中胚层肾瘤超声特征:4例胎儿中胚层肾瘤均于晚孕期被检出,发现肿块时径线均较大(直径均> 6 cm),均为单侧肾区单发肿块,实性或囊实性;肿块与周围组织分界清,其中 3 例可于肿块一极见少许残肾回声,彩色多普勒超声显示肿块内部均可见较丰富的“树枝状”血流信号,均合并羊水多。产前胎儿磁共振影像均显示肿块内部有不同程度坏死灶,肿块边界清楚,周边可见受压的残肾组织。随访结果:3 例孕妇选择终止妊娠,1 例出生后行患侧肾切除手术,预后良好。超声与病理类型对照:1 例超声显示为完全实性肿块,病理组织学类型为经典型;而囊实性肿块及实性为主肿块 3 例,病理组织学类型为细胞型或混合型。

结论

中胚层肾瘤是胎儿期常见的肾肿瘤,有特征性的超声表现,影像学特征与病理组织学类型有一定相关性,超声与磁共振联合诊断有助于正确诊断而减少误诊。

Objective

To summarize the ultrasonographic findings of fetal mesoblastic nephroma and compare them with pathological findings.

Methods

The ultrasonographic images, magnetic resonance images, pathological types, and follow-up results of four cases of fetal mesoblastic nephroma discovered by prenatal ultrasound at Maternal and Child Health Hospital of Hubei Province from January 2003 to December 2018 were analyzed retrospectively.

Results

All the four cases of mesoblastic nephroma were detected in late pregnancy. The diameter of all the masses was larger than 6 cm. All masses were single, unilateral, and solid or cystic solid. The boundary between the mass and surrounding tissue was clear. A little residual kidney echo could be seen in three cases. Abundant dendritic blood flow signals could be detected inside the masses by color Doppler ultrasonography, and all of them were complicated with amniotic fluid. The prenatal fetal MRI imaging features showed different necrotic ranges inside the mass, the boundary of the mass was clear, and the pressed residual renal tissue was visible around it. Three pregnant women terminated pregnancy, and one case underwent ipsilateral nephrectomy after birth, with a good prognosis. In one case showing a complete solid mass, the pathological tissue type was classical, while a cystic-solid mass or mass with predominant solid components was found in three cases, in which the tissue type was cellular or mixed type.

Conclusion

Mesoblastic nephroma is a common fetal renal tumor with characteristic ultrasonographic features, and there is a certain correlation between imaging features and pathological types. The combined diagnosis of ultrasound and magnetic resonance imaging is helpful to diagnose correctly and reduce misdiagnosis.

表1 4例中胚层肾瘤胎儿临床资料、超声声像图特征及产后组织病理学类型
表2 4例中胚层肾瘤胎儿超声表现与病理类型对照(检出例数/总例数)
图1 胎儿实质为主型中胚层肾瘤(例3)超声与病理大体标本对照图。图a、b 超声声像图示胎儿肾区肿块实性为主,内可见部分低回声区;患侧肾上腺可显示肿块内部“树枝状”血流信号(图b);大体病理标本显示肿瘤内部可见小片坏死灶(图c)
图2 胎儿混合型中胚层肾瘤(例4)超声与病理大体标本对照图。图a,b 超声声像图示胎儿肾区囊实性肿块,边界清,内可见不规则无回声区;图c 大体病理标本显示肿瘤内部可见多片囊性坏死灶
1
Chaudry G, Perez-Atayde AR, Ngan BY, et al. Imaging of congenital mesoblastic nephroma with pathological correlation [J]. Pediatr Radiol, 2009, 39(10): 1080-1086.
2
Bayindir P, Guillerman RP, Hicks MJ, et al. Cellular mesoblastic nephroma (infantile renal fibrosarcoma): institutional review of the clinical, diagnostic imaging, and pathologic features of a distinctive neoplasm of infancy [J]. Pediatr Radiol, 2009, 39(10): 1066-1074.
3
Gooskens SL, Houwing ME, Vujanic GM, et al. Congenital mesoblastic nephroma 50 years after its recognition: a narrative review [J]. Pediatr Blood Cancer, 2017, 64(7): 1-9.
4
Bolande RP, Brough AJ, Izant RJ, et al. Congenital mesoblastic nephroma of infancy. A report of eight cases and the relationship to Wilms' tumor [J]. Pediatrics, 1967, 40(2): 272-278.
5
Argani P, Ladanyi M. Recent advances in pediatric renal neoplasia [J]. Adv Anat Pathol, 2003, 10(5): 243-260.
6
Montaruli E, Fouquet V. Prenatal diagnosis of congenital mesoblastic nephroma [J]. Fetal Diagn Ther, 2013, 33(1): 79-80.
7
Linam LE, Yu X, Calvo-Garcia MA, et al. Contribution of magnetic resonance imaging to prenatal differential diagnosis of renal tumors: report of two cases and review of the literature [J]. Fetal Diagn Ther, 2010, 28(2): 100-108.
8
Takahashi H, Ohkuchi A, Kuwata T, et al. Congenital mesoblastic nephroma: its diverse clinical features -a literature review with a case report [J]. J Obstet Gynaecol, 2016, 36(3): 340-344.
9
Kim CH, Kim YH, Cho MK, et al. A case of fetal congenital mesoblastic nephroma with oligohydramnios [J]. J Korean Med Sci, 2007, 22(2): 357-361.
10
Chen WY, Lin CN, Chao CS, et al. Prenatal diagnosis of congenital mesoblastic nephroma in mid-second trimester by sonography and magnetic resonance imaging [J]. Prenat Diagn, 2003, 23(11): 927-931.
11
Marry M, Grundy P, Graf N, et al. Characteristics and survival of 750 children diagnosed with a renal tumor in the first seven months of life: A collaborative study by the SIOP/GPOH/SFOP, NWTSG, and UKCCSG wilms tumor study groups [J]. Pediatr Blood Cancer, 2008, 50(6): 1130-1134.
12
Daniel J, Ruzic A, Dalland J, et al. Management of mixed type congenital mesoblastic nephroma: case series and review of the literature [J]. J Neonatal Perinatal Med, 2017, 10(1): 113-118.
13
Santos LG, Carvalho JS, Reis MA, et al. Cellular congenital mesoblastic nephroma: case report [J]. J Bras Nefrol, 2011, 33(1): 109-112.
14
邹继珍, 何偲, 白云, 等. 婴幼儿先天性中胚层肾瘤的临床病理分析 [J]. 中国小儿血液与肿瘤杂志, 2015, 20 (1): 32-37.
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