Journal of Neonatal Surgery (Jul 2018)

Neumann’s Tumor - A Rare Neonatal Tumor

  • Ceyhan Sahin,
  • Zeliha Akış yıldız,
  • Aytekin Kaymakcı,
  • Ozgül Gergin tinay

DOI
https://doi.org/10.21699/jns.v7i3.777
Journal volume & issue
Vol. 7, no. 3

Abstract

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Neumann’s tumor, also known as congenital granular cell tumor, congenital myoblastoma, congenital epulis, was first described by Neumann in 1871. It’s a rare cause of newborn’s intraoral masses. they are usually on the maxilla and soliter , they can rarely be seen on the mandibula and multiple. Even if it is not clinically symptomatic, surgical resection is performed because of its cosmetic appearance, negative psychological effect on the family , differential diagnosis and treatment. Neumann’s tumor is fully cured by surgical resection because it does not show recurrence or metastasis after excision.

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