scholarly journals BASAL CELL ADENOMA: A RARE CASE REPORT WITH IMMUNOHISTOCHEMICAL ANALYSIS

2018 ◽  
Vol 4 (3) ◽  
pp. 227-229
Author(s):  
Anjali Sharma ◽  
Deshant Agarwal ◽  
Anil Kumar Gupta ◽  
Chandralekha L Pande
2018 ◽  
Vol 2 (3) ◽  
pp. 55
Author(s):  
Ruchi Bhuyan ◽  
Pinali Das ◽  
Shayari Niyogi ◽  
SanatKumar Bhuyan

2019 ◽  
Vol 10 (9) ◽  
pp. 1705
Author(s):  
Harsh Mohan Pathak ◽  
Santosh Kumar Subudhi ◽  
Satya Patnaik ◽  
Swagatika Panda ◽  
Kalyan Sundar Pal

Author(s):  
Pietry Dy Tarso Ina Alves Malaquias ◽  
Lucas Depoli De Figueiredo ◽  
André Lucas ◽  
Douglas Bertazo Musso ◽  
Thassio Vidal Assis ◽  
...  

2015 ◽  
Vol 11 (4) ◽  
pp. 1023 ◽  
Author(s):  
HarkanwalPreet Singh ◽  
SurinderPal Singh Sodhi ◽  
RamandeepSingh Brar ◽  
Tajinder Kaur ◽  
Rohan Dhawan

2015 ◽  
Vol 5 (3) ◽  
pp. 184-187
Author(s):  
Pratik Dipak Shah ◽  
Srijon Mukherji

ABSTRACT Basal cell adenoma (BCA) is a significantly rare benign salivary gland neoplasm that includes isomorphic basaloid cells. Presence of myoepithelial cell is a characteristic of this tumor. Basal cell adenoma accounts for only 1 to 2% of all salivary gland epithelial tumors. The goal of the paper is to report a rare case of tubular type of BCA arising from parotid gland and discuss its management. How to cite this article Shah PD, Mukherji S. Tubular Type of Basal Cell Adenoma of Parotid Gland: A Rare Entity. J Contemp Dent 2015;5(3):184-187.


2021 ◽  
Vol 4 (3) ◽  
Author(s):  
Ramesh Mahadev Tambat ◽  
Sreenivas M. D. ◽  
Tejas A. P. ◽  
Nitin Kumar K ◽  
Sadiq Nawaz F ◽  
...  

2016 ◽  
Vol 121 (3) ◽  
pp. e62-e64 ◽  
Author(s):  
Emanuela Ortolani ◽  
Antonella Polimeni ◽  
Libero Lauriola ◽  
Antonella Coli

2014 ◽  
Vol 5 (1) ◽  
pp. 39-41
Author(s):  
Shahanavaj Imam Husen Khaji ◽  
Gayathri H Kulkarni ◽  
Harish S Kulkarni ◽  
Suryakant B Metkari ◽  
Reshma Kulkarni

ABSTRACT Nevoid basal cell carcinoma syndrome is a syndrome with wide variety of manifestations ranging from oral lesions to skeletal deformities. It calls for due responsibility of maxillofacial surgeon to diagnose the syndrome because very often they are the first health professionals to see the patient for the treatment of keratocystic odontogenic tumor. Keratocystic odontogenic tumor (KCOT) has been the topic of numerous investigators and is known for its potentially aggressive behavior and significant rate of recurrences. Keratocystic odontogenic tumor often occurs as a solitary lesion, and in some instances multiple keratocysts may occur in association with a syndrome called Gorlin-Goltz syndrome (nevoid basal cell carcinoma, jaw cyst bifid rib basal cell nevus syndrome). Here, we present a case of multiple keratocysts in the mandible in association with skeletal, ocular and cutaneous anomalies in the given clinical scenario which has profound relevance in the clinical dental practice. How to cite this article Kulkarni GH, Khaji SI, Kulkarni HS, Metkari SB, Kulkarni R. Multiple Keratocysts of the Mandible in Association with Multiple Basal Epithelioma, Jaw Cysts and Bifid Rib Syndrome: A Rare Case Report. Int J Head Neck Surg 2014;5(1):39-41.


2014 ◽  
Vol 4 (2) ◽  
pp. 83-87
Author(s):  
Yayoi Yamamoto ◽  
Rie Horii ◽  
Yukiko Sato ◽  
Kouichi Ikebata ◽  
Takuji Iwase ◽  
...  

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