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CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2018; 39(03): 413-414
DOI: 10.4103/ijmpo.ijmpo_245_17
Case Report

Unusual Presentation of Wilms' Tumor as Umbilical Granuloma

Shalini Gajanan Hegde
Department of Pediatric Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India
,
Prema Menon
Department of Pediatric Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India
,
Katragadda Lakshmi Narasimha Rao
Department of Pediatric Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India
,
Ritambhra Nada
Department of Histopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India
› Institutsangaben Financial support and sponsorship Nil.
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Abstract

We report an unusual presentation of a Wilms' tumor in an 8-month-old child, incidentally detected by ultrasonography for an umbilical granuloma. A patent vitellointestinal duct anomaly required surgical excision in the same sitting as the nephroureterectomy. The case is reported for the unusual coexistence and the management implications.

Keywords

Incidental diagnosis - umbilical granuloma - vitellointestinal duct anomaly - Wilms' tumor


Publikationsverlauf

Artikel online veröffentlicht:
17. Juni 2021

© 2018. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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  • References

  • 1 Sarwar U, Javed M, Wright T, Dawson A, Wilson-Jones N. These umbilical lesions weren't granulomas after all. J Fam Pract 2016; 65: E1-3
    Google Scholar
  • 2 Weirich A, Ludwig R, Graf N, Abel U, Leuschner I, Vujanic GM. et al. Survival in nephroblastoma treated according to the trial and study SIOP-9/GPOH with respect to relapse and morbidity. Ann Oncol 2004; 15: 808-20
    CrossrefPubMedGoogle Scholar
  • 3 Kadian YS, Verma A, Rattan KN, Kajal P. Vitellointestinal duct anomalies in infancy. J Neonatal Surg 2016; 5: 30
    CrossrefPubMedGoogle Scholar
  • 4 Larbcharoensub N, Pongtippan A, Pangpunyakulchai D, Phongkitkarun S, Lertsithichai P, Dejthevaporn TS. et al. Sister mary joseph nodule caused by metastatic desmoplastic small round cell tumor: A clinicopathological report. Mol Clin Oncol 2016; 5: 557-61
    CrossrefPubMedGoogle Scholar
  • 5 Lamb MG, Aldrink JH, O'Brien SH, Sinha H, Arnold MA, Ranalli MA. et al. Renal tumors in children younger than 12 months of age: A 65-year single institution review. J Pediatr Hematol Oncol 2017; 39: 103-7
    CrossrefPubMedGoogle Scholar
  • 6 Li A, Asch M, Lasky J, Sieger L, Lee SL. et al. Neonatal. Neonat 2012; 34: e193-4
    Google Scholar