scholarly journals Colonic granular cell tumor: Report of 11�cases and management with review of the literature

Author(s):  
Yahua Chen ◽  
Yangyang Chen ◽  
Xiaoqiong Chen ◽  
Liang Chen ◽  
Wei Liang
2004 ◽  
Vol 10 (6) ◽  
pp. 528-531 ◽  
Author(s):  
Adebowale Adeniran ◽  
Hikmat Al-Ahmadie ◽  
Mary C. Mahoney ◽  
Toni M. Robinson-Smith

2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Ramin Niknam ◽  
Kamran Bagheri Lankarani ◽  
Bita Geramizadeh

Gastrointestinal granular cell tumors are uncommon. The most common site of gastrointestinal granular cell tumor (GCT) is esophagus. We report a case of esophageal GCT incidentally diagnosed by endoscopy. The lesion was evaluated by endoscopic ultrasonography and resected using the endoscopic technique without complication.


Neurosurgery ◽  
1998 ◽  
Vol 42 (1) ◽  
pp. 166-170 ◽  
Author(s):  
Bernhard Schaller ◽  
Eberhard Kirsch ◽  
Markus Tolnay ◽  
Thomas Mindermann

1983 ◽  
Vol 14 (2) ◽  
pp. 125-129
Author(s):  
Zeynel A Karcioglu ◽  
Gregory L Hemphill ◽  
Brandon M Wool

2005 ◽  
Vol 29 (1) ◽  
pp. 69-74 ◽  
Author(s):  
Robert Brannon ◽  
Payal Anand

Clinicopathologic studies on the granular cell tumor, a submucosal benign soft-tissue neoplasm, have not addressed the pediatric and adolescent population. This study of patients from birth to 19 years of age describes clinically and microscopically 10 new cases and combines them with 24 well-documented pediatric cases previously published in the English-language literature. Of the 34, patient ages ranged from 3 to 19 years (mean age 14.5 years) with a female-to-male ratio of 3.3 to 1. The most common location was the tongue (50%) and lips (25%). In neoplasms whose epithelial findings were documented microscopically, a reactive pseudoepitheliomatous (pseudocarcinomatous) hyperplasia of the overlying epithelium occurred in 29%. The recurrence rate was less than 10% following conservative surgical excision. This study reveals that an oral granular cell tumor in the first decade of life is an uncommon event and discusses the importance of differentiating between squamous cell carcinoma and granular cell tumor.


2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Yara A. Alnashwan ◽  
Khaled A. H. Ali ◽  
Samir S. Amr

Malignant granular cell tumor (MGCT) is a rare high-grade mesenchymal tumor of Schwann cell origin. MGCTs commonly affect thigh, extremity, and trunk; however, involvement of the abdominal wall is quite rare. It has poor prognosis with 39% mortality rate in 3-year interval. We report a 50-year-old female who had MGCT arising in the anterior abdominal wall and developed massive metastatic deposits in both lungs and in the right inguinal lymph nodes, with prolonged survival for 11 years. A brief review of the literature is presented.


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.


2000 ◽  
Vol 4 (4) ◽  
pp. 245-251 ◽  
Author(s):  
Abdul M. Al-Ghamdi ◽  
Julia D.A. Flint ◽  
Nestor L. Muller ◽  
Ken C. Stewart

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