Antenatally Diagnosed Wilms' Tumour - A Case Report

Wilms' tumour (WT) is seldom seen in a neonate and prenatal diagnosis is rare. We present a case of antenatally diagnosed left sided WT with features of hydrops foetalis in a girl baby. Emergency LSCS was done at 34 weeks of gestation for foetal distress. Patient required mechanical ventilation...

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Main Authors: Yogesh Kumar Sarin (Author), SK Rahul (Author), S Sinha (Author), N Khurana (Author), S Ramji (Author)
Format: Book
Published: EL-Med-Pub, 2014-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Yogesh Kumar Sarin  |e author 
700 1 0 |a SK Rahul  |e author 
700 1 0 |a S Sinha  |e author 
700 1 0 |a N Khurana  |e author 
700 1 0 |a S Ramji  |e author 
245 0 0 |a Antenatally Diagnosed Wilms' Tumour - A Case Report 
260 |b EL-Med-Pub,   |c 2014-01-01T00:00:00Z. 
500 |a 10.21699/jns.v3i1.114 
500 |a 2226-0439 
520 |a Wilms' tumour (WT) is seldom seen in a neonate and prenatal diagnosis is rare. We present a case of antenatally diagnosed left sided WT with features of hydrops foetalis in a girl baby. Emergency LSCS was done at 34 weeks of gestation for foetal distress. Patient required mechanical ventilation for birth asphyxia and congestive cardiac failure. After stabilization, gross total resection of the tumour was done on day 4 of life. Histopathology HPE confirmed classical WT (stage I). Unfortunately, the patient died on the second postoperative day despite all supportive measures. 
546 |a EN 
690 |a Wilms' tumour 
690 |a Hydrops foetalis 
690 |a Antenatal detection 
690 |a Pediatrics 
690 |a RJ1-570 
690 |a Surgery 
690 |a RD1-811 
655 7 |a article  |2 local 
786 0 |n Journal of Neonatal Surgery, Vol 3, Iss 1 (2014) 
787 0 |n https://jneonatalsurg.com/ojs/index.php/jns/article/view/72 
787 0 |n https://doaj.org/toc/2226-0439 
856 4 1 |u https://doaj.org/article/4746d129600b407aa22fc6e505a0cb15  |z Connect to this object online.