Bilateral adrenal neuroblastoma

Background: Bilateral tumors in double organs like bilateral adrenal neuroblastoma are highly rare. Few cases have been reported in the literature. Case reports: A full-term male infant, 11 months old, had an abdominal mass diagnosed by triphasic abdominal CT as bilateral adrenal neuroblastoma. The...

Full description

Saved in:
Bibliographic Details
Main Authors: Sarah Magdy Abdelmohsen (Author), Mohamed Abdelkader Osman (Author), Tarek Abdelazeem Sabra (Author), Ahmed K. Ali (Author), Ahmed Gamal Abdelmalek Moursi (Author), Basel Abdelazeem (Author), Marwa T. Hussien (Author)
Format: Book
Published: Elsevier, 2023-02-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background: Bilateral tumors in double organs like bilateral adrenal neuroblastoma are highly rare. Few cases have been reported in the literature. Case reports: A full-term male infant, 11 months old, had an abdominal mass diagnosed by triphasic abdominal CT as bilateral adrenal neuroblastoma. The case was stage 1, and the management was bilateral adrenalectomy. Discussion: When the neuroblastoma mass measures less than 5 cm in diameter, the infant can likely be safely supervised without cytoreduction surgery or histological confirmation of the tumor, but if the tumour progressively increases in size or the size is greater than 5 cm, then surgery is essential. Conclusion: Surgery is the best option when an infant has bilateral large localized adrenal neuroblastoma.
Item Description:2213-5766
10.1016/j.epsc.2022.102518