scholarly journals Congenital Granular Cell Tumour: Report of a case with review of literature and differential diagnosis.

2021 ◽  
Author(s):  
arpita singh ◽  
Snehashish Ghosh ◽  
Anjani Yadav ◽  
Anuja Panthee
Keyword(s):  
Differential Diagnosis ◽  
Caesarean Section ◽  
Prenatal Screening ◽  
Benign Lesion ◽  
Granular Cell ◽  
Cell Tumour ◽  
Granular Cell Tumour ◽  
Review Of Literature ◽  
Normal Delivery

Congenital Granular Cell Tumour (CGCT) is a rare benign lesion and presents in newborn as fibrous mass arising from the alveolus.The prenatal screening of lesion can help in parent counselling, determining the complications, as larger size lesion may interfere with normal delivery and require caesarean section.

scholarly journals Granular Cell Tumour of The Vulva: A Case Report

1970 ◽  
Vol 3 (1) ◽  
pp. 28-30
Author(s):  
SM Khodeza ◽  
Nahar Begum ◽  
Nishat Begum
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Benign Lesion ◽  
Granular Cell ◽  
Cell Tumour ◽  
Granular Cell Tumour ◽  
Duct Cyst ◽  
Clinical Presentations ◽  
Neural Origin ◽  
Granular Cell Tumours

Vulvar granular cell tumours are uncommon neoplasms of neural origin. The clinical presentations, surgical findings and histology of Granular Cell Tumour (GCT) of the vulva in a 50 year old lady is presented. Although rare, this benign lesion must be considered in the differential diagnosis of the labia majora masses, such as Bartholin,s duct cyst, Lipoma, Papilloma, Hydradenoma and Fibroma. DOI: http://dx.doi.org/10.3329/akmmcj.v3i1.10111 AKMMCJ 2012; 3(1): 28-30

scholarly journals Surgical Excision of Orbital Progressive Granular Cell Tumour

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Demetrio Germanò ◽  
Hossein Mostafa Elbadawy ◽  
Diego Ponzin ◽  
Daniele Ferro ◽  
Leonardo Priore
Keyword(s):  
Ct Scan ◽  
Benign Lesion ◽  
Granular Cell ◽  
Surgical Excision ◽  
Cell Tumour ◽  
Granular Cell Tumour ◽  
Initial Examination ◽  
Orbital Mass ◽  
S 100 ◽  
Substantial Progress

Granular cell tumour (GCT) is mostly benign lesion first described by Abrikossoff and named after him. Most cases are reported in the head and neck area, where the tongue is the most common site. Here we review previous cases in the literature for GCT in the orbit and present a new case. A 49-year-old male presented with apparent exophthalmos. Examination of the patient revealed the presence of a mass in the bottom side of the orbit. A substantial progress was noted after two months from the initial examination using computed tomography (CT) scan. An orbital mass was extracted and histological analysis showed signs typical for GCT. Immunohistochemistry was positive for S-100; the biopsy showed no mitotic or necrotic areas. Proptosis was resolved after surgery and a six-year follow-up CT scan was performed. We conclude that rapid progress of the tumour does not necessarily suggest malignancy.

scholarly journals Granular Cell Tumour of the Bile Duct in Association with Intrahepatic Bile Duct Adenomas

1994 ◽  
Vol 8 (2) ◽  
pp. 92-96
Author(s):  
F Schweiger ◽  
J Radhi ◽  
FW Coop ◽  
RW Murphy
Keyword(s):  
Bile Duct ◽  
Benign Lesion ◽  
Intrahepatic Bile Duct ◽  
Granular Cell ◽  
Metastatic Carcinoma ◽  
Cell Tumour ◽  
Focal Liver Lesions ◽  
Caucasian Woman ◽  
Granular Cell Tumour ◽  
Almost All

Granular cell tumour of the extrahepatic biliary tract is a rare benign lesion likely of neurogenic origin. Review of the previously reported cases indicates that almost all patients are female, and the majority is Black. Symptoms usually are those of biliary obstruction or cholecystitis. Surgical resection of the tumour is curative. Intrahepatic bile duct adenoma is another rare benign biliary neoplasm that does not manifest clinically but can be confused with metastatic carcinoma, cholangiocarcinoma or other focal liver lesions at laparotomy or autopsy. The authors report the case of an asymptomatic Caucasian woman with biochemical evidence of liver disease who had a granular cell tumour of the bile duct as well as several intrahepatic bile duct adenomas.

scholarly journals CONGENITAL GRANULAR CELL TUMOUR : A RARE CASE REPOR

2020 ◽  
pp. 1-2
Author(s):  
Sabari Devi ◽  
Waziha Ahmed
Keyword(s):  
Smooth Muscle ◽  
Smooth Muscle Cells ◽  
Recurrence Rate ◽  
Rare Case ◽  
Benign Lesion ◽  
Granular Cell ◽  
Surgical Excision ◽  
Cell Tumour ◽  
Granular Cell Tumour ◽  
Feeding Problems

Congenital granular cell tumour/ epulis (CGCE) is a rare benign lesion of the newborn. It was first described in 1871 by Neumann. It usually arises from the alveolar mucosa of neonates and may cause respiratory and feeding problems. The exact histogenesis is unclear. The proposed source of origin includes undifferentiated mesenchymal cells, odontogenic epithelial, pericytes, fibroblasts, smooth muscle cells. Treatment involves surgical excision and and its curative with rare recurrence rate.

scholarly journals Esophageal granular cell tumour: A case report and review of literature

2020 ◽  
Vol 3 (2) ◽  
pp. 106-108
Author(s):  
Dr. Shefali Agarwal ◽  
Dr. Deepti Gupta ◽  
Dr. Anjali Tewari ◽  
Dr. Nupur Trivedi
Keyword(s):  
Case Report ◽  
Granular Cell ◽  
Cell Tumour ◽  
Granular Cell Tumour ◽  
Review Of Literature

GRANULAR CELL TUMOUR IN A MALE BREAST

1973 ◽  
Vol 2 (22) ◽  
pp. 1010-1011 ◽  
Author(s):  
Stewart Hart ◽  
Lorna Sisely
Keyword(s):  
Granular Cell ◽  
Male Breast ◽  
Cell Tumour ◽  
Granular Cell Tumour
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