Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Pediatric renal rhabdoid tumor: Imaging features and diagnostic challenges of a rare and aggressive neoplasm.

Radiology case reports·2025
Same author

Primary sebaceous gland carcinoma of the bulbar conjunctiva.

Journal francais d'ophtalmologie·2025
Same author

A rare localization of Ewing's Sarcoma in the coracoid process: A case report and literature review on scapular Ewing's sarcomas.

Radiology case reports·2024
Same author

[A rare conjunctival nevus: Spitz nevus].

Journal francais d'ophtalmologie·2024
Same author

Intramedullary spinal schistosomiasis: A case report and review of the literature.

International journal of surgery case reports·2024
Same author

Control and treatment of type 2 diabetes in private patients in the Egyptian "DIACONTROL study".

European review for medical and pharmacological sciences·2023

Related Experiment Video

Updated: Jun 8, 2026

Application of Robot-assisted Pancreaticobiliary Junction Resection in Benign Duodenal Tumors
03:37

Application of Robot-assisted Pancreaticobiliary Junction Resection in Benign Duodenal Tumors

Published on: December 20, 2024

[Botryoid Wilms tumor extending into the duodenum].

N Lamalmi1, L Rouas, N Cherradi

  • 1Hôpital d'Enfants, Rabat, Maroc. abiradil@hotmail.com

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|October 15, 2010
PubMed
Summary
This summary is machine-generated.

We describe a rare case of botryoid Wilms tumor, a type of nephroblastoma, extending into the duodenum. This finding is unique as it

More Related Videos

Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib
06:43

Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib

Published on: April 3, 2026

Robotic Duodenum-preserving Total Pancreatic Head Resection for Intraductal Papillary Mucinous Neoplasms
10:10

Robotic Duodenum-preserving Total Pancreatic Head Resection for Intraductal Papillary Mucinous Neoplasms

Published on: April 17, 2026

Related Experiment Videos

Last Updated: Jun 8, 2026

Application of Robot-assisted Pancreaticobiliary Junction Resection in Benign Duodenal Tumors
03:37

Application of Robot-assisted Pancreaticobiliary Junction Resection in Benign Duodenal Tumors

Published on: December 20, 2024

Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib
06:43

Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib

Published on: April 3, 2026

Robotic Duodenum-preserving Total Pancreatic Head Resection for Intraductal Papillary Mucinous Neoplasms
10:10

Robotic Duodenum-preserving Total Pancreatic Head Resection for Intraductal Papillary Mucinous Neoplasms

Published on: April 17, 2026

Area of Science:

  • Pediatric Oncology
  • Surgical Pathology

Background:

  • Wilms tumor (nephroblastoma) is the most common pediatric renal malignancy.
  • Botryoid Wilms tumor is a rare macroscopic variant, often presenting as a polypoid intrapelvic mass.
  • Differential diagnosis includes botryoid rhabdomyosarcoma.

Observation:

  • A 14-month-old boy presented with a painful abdominal mass.
  • Radiology showed a large, heterogeneous renal mass extending into the ureter.
  • Surgical resection revealed duodenal extension of the tumor.

Findings:

  • Pathologic diagnosis confirmed mixed-type nephroblastoma, SIOP 2001 stage III.
  • The tumor exhibited unusual extension into the second portion of the duodenum.
  • Postoperative chemotherapy was administered.

Implications:

  • This case represents the first reported instance of botryoid nephroblastoma extending into the digestive system.
  • Highlights the importance of considering rare presentations in pediatric renal masses.
  • Successful management with nephroureterectomy and chemotherapy offers a positive prognosis.