scholarly journals Neumann’s Tumor - A Rare Neonatal Tumor

2018 ◽  
Vol 7 (3) ◽  
pp. 40
Author(s):  
Ceyhan Sahin ◽  
Zeliha Akış yıldız ◽  
Aytekin Kaymakcı ◽  
Ozgül Gergin tinay

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.

1997 ◽  
Vol 55 (11) ◽  
pp. 1356-1359 ◽  
Author(s):  
Jingo Kusukawa ◽  
Sachiko Kuhara ◽  
Chihiro Koga ◽  
Toshirou Inoue

2008 ◽  
Vol 33 (2) ◽  
pp. 167-170 ◽  
Author(s):  
Henrique Castilhos Ruschel ◽  
Letícia Pozzi Beilke ◽  
Rodrigo Pozzi Beilke ◽  
Paulo Floriani Kramer

Congenital epulis of newborn is a rare benign tumor that is also known as a congenital granular cell tumor. The objective of this article was to describe and discuss the case of a newborn girl with a pedunculated mass in the left anterior maxillary alveolar margin diagnosed as congenital epulis. Conservative treatment was adopted and the lesion spontaneously regressed.


2020 ◽  
Vol 1 (4) ◽  
Author(s):  
Alexander J Schupper ◽  
Frank J Yuk ◽  
Hongyan Zou ◽  
Sadhna Ahuja ◽  
Nadejda M Tsankova ◽  
...  

Abstract BACKGROUND AND IMPORTANCE Granular cell tumors (GCTs) of the sellar and suprasellar regions are rare tumors that may be managed surgically by multiple strategies. The technical approaches for these tumors have rarely been described in the literature. CLINICAL PRESENTATION We introduce the case of a patient presenting with dizziness and headaches who was found to have a suprasellar and retrochiasmatic mass and eventually underwent surgical resection. We discuss the characteristics of this tumor, and the current state of the literature. Also included are details regarding the surgical approach utilized in this case, and a discussion of the various surgical approaches for this type of tumor. CONCLUSION There are several approaches for the surgical resection of suprasellar GCTs, and the approach utilized may depend on patient and/or surgeon considerations. Patient-specific considerations must be made to ensure maximal safe resection of these lesions.


2006 ◽  
Vol 17 (3) ◽  
pp. 594-598 ◽  
Author(s):  
Dominick I. Golio ◽  
Sujit Prabhu ◽  
Erik F. Hauck ◽  
Bita Esmaeli

Pituitary ◽  
2019 ◽  
Vol 22 (6) ◽  
pp. 633-639 ◽  
Author(s):  
Abdul-Kareem Ahmed ◽  
Hassan Y. Dawood ◽  
David J. Cote ◽  
Tejus A. Bale ◽  
Umberto De Girolami ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
Preston Gardner ◽  
Arlene Rozzelle

Congenital granular cell tumors are infrequently occurring masses occurring on a neonate’s gingiva/alveolus. These lesions are benign with no noted malignant transformation, and treatment of excision is based on its effect on the neonate’s respiratory ability and/or nutritional intake. The purpose of this review is to discuss a case of a congenital granular cell tumor and its treatment and review of the literature including demographics, histopathology, and operative treatment.


1975 ◽  
Vol 40 (2) ◽  
pp. 270-277 ◽  
Author(s):  
C.T. Dixter ◽  
M.S. Konstat ◽  
J.L. Giunta ◽  
E. Schreier ◽  
G.E. White

2009 ◽  
Vol 20 (3) ◽  
pp. 976-977 ◽  
Author(s):  
Sirin Guven ◽  
Aytekin Kaymakci ◽  
Muhammet Serdar Bugday ◽  
Muberra Yilmaz

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