scholarly journals Granular Cell Tumour of Breast-An Enigmatic Entity-Case Report with Emphasis on Role of Frozen Section

Author(s):  
Pooja Jain ◽  
Geetha Vasudevan ◽  
Padmapriya Jaiprakash ◽  
Stanley Mathew
2007 ◽  
Vol 121 (5) ◽  
pp. 506-509 ◽  
Author(s):  
C Holton ◽  
H E Cruickshank ◽  
A S High ◽  
K Maclennan ◽  
Z G G Makura

Granular cell tumours of the larynx are a very rare cause of persistent hoarse or husky voice in children. We report the case of a 13-year-old girl who presented with a three-year history of progressively huskier voice. We discuss the presentation, location and diagnosis of the tumour. In addition, we present a method of surgical treatment of the tumour, involving the hitherto unreported technique of laser excision and frozen section of the lesion.


2016 ◽  
Vol 49 (4) ◽  
pp. 275
Author(s):  
P Appiah-Thompson ◽  
KK Baidoo

Pathology ◽  
2016 ◽  
Vol 48 ◽  
pp. S132
Author(s):  
Kais Kasem ◽  
Lakshmy Nandakumar ◽  
Mark Appleyard ◽  
Mahendra Singh

2007 ◽  
Vol 19 (3) ◽  
pp. 167-169
Author(s):  
Hiroshi Matsuura ◽  
Katsura Tsubota ◽  
Kazuo Sano ◽  
Mikiko Nakamura ◽  
Kazuki Miyauchi ◽  
...  

1970 ◽  
Vol 3 (1) ◽  
pp. 28-30
Author(s):  
SM Khodeza ◽  
Nahar Begum ◽  
Nishat Begum

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


2020 ◽  
Vol 13 (7) ◽  
pp. e232851
Author(s):  
Christopher Hogan ◽  
Vikas Acharya ◽  
Yvonne Tsitsiou ◽  
Ali Taghi

We present a rare case of a paediatric laryngeal granular cell tumour (GCT) of the vocal cord. GCTs are rare clinical entities, thought to arise from Schwann cells. There are only a handful of paediatric laryngeal GCTs in the literature, and therefore, little is known regarding their natural history or preferred management strategies. In this case report, we discuss the incidence, aetiopathogenesis, presentation and management of a laryngeal GCT in an 11-year-old girl, who presented with dysphonia. We believe that this case will aid otolaryngologists in the management of paediatric patients with the common dysphonia.


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