Granular Cell Tumor of the Intrapancreatic Common Bile Duct: One Case Report and Review of the Literature

2004 ◽  
Vol 28 (3) ◽  
pp. 171-176 ◽  
Author(s):  
Guiseppe Altavilla ◽  
Maurizio Brotto ◽  
Graziella Busatto ◽  
Chiara Boccu` ◽  
Luigi Ragni
2017 ◽  
Vol 8 (4) ◽  
pp. 132-136
Author(s):  
Anastasios Katsourakis ◽  
Ioannis Dimitriou ◽  
Efthimios Chatzitheoklitos ◽  
Danai Chourmouzi ◽  
George Noussios

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.


1987 ◽  
Vol 4 (3) ◽  
pp. 176-180
Author(s):  
Arie C. van der Ham ◽  
Willem S. Meijer ◽  
Harry F.G.M. van den Ingh ◽  
Hendrik A. van Essen

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

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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