A rare case of endobronchial and lung metastasis in basal cell carcinoma

Author(s):  
Sameer Verma ◽  
Sonu Sahni ◽  
Shahzad Zeb ◽  
Michael J. Esposito ◽  
Arunabh Talwar
2015 ◽  
Vol 8 (3) ◽  
pp. 536-539
Author(s):  
Ellen Toyonaga ◽  
Hiroo Hata ◽  
Chihiro Nakayama ◽  
Erina Homma ◽  
Toshiyuki Miyashita ◽  
...  

Nevoid basal cell carcinoma syndrome (NBCCS), also known as Gorlin syndrome, is a rare hereditary condition characterized by a wide range of developmental abnormalities and a predisposition to neoplasms. The syndrome consists of early-onset and/or multiple BCC. Herein we report a rare NBCCS case in which the first BCC onset occurred in the groin area. To the best of our knowledge, there have been no reports of first-onset BCC in the groin area in an NBCCS patient of any race.


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.


1997 ◽  
Vol 20 (2) ◽  
pp. 110-111 ◽  
Author(s):  
A. Schwabegger ◽  
M. Ninkovic ◽  
G. Wechselberger ◽  
B. Zelger ◽  
H. Anderl

2016 ◽  
Vol 61 (4) ◽  
pp. 443 ◽  
Author(s):  
Naoko Okiyama ◽  
Kana Shibao ◽  
Ryota Tanaka ◽  
Hitoshi Maruyama ◽  
Yasuhiro Fujisawa ◽  
...  

Author(s):  
Bhumika Rath ◽  
Ankit Rattan ◽  
Z U.Khan ◽  
C Chiranjibi ◽  
Sourav Subham

Author(s):  
Anita Moraskar ◽  
Shema Shirodkar ◽  
Dheeraj Lambor ◽  
Surender Kumar

2011 ◽  
Vol 2 (4) ◽  
pp. 342-345
Author(s):  
Vinod Kumar ◽  
Chaitanya Babu ◽  
Geetanshu Dawar

ABSTRACT Here, we report a case of keratocystic odontogenic tumor occurring bilaterally in a male patient in fourth decade of life. This case is different from bilateral lesions of keratocystic odontogenic tumor which are most commonly parakeratinized and are associated with syndromes like nevoid basal cell carcinoma syndrome. In our case, we could not find out any syndromic association and furthermore histopathology was in line of orthokeratinization.


2020 ◽  
Vol 33 (4) ◽  
Author(s):  
Matthias Holzbauer ◽  
Susanne Groß ◽  
Georg M. Huemer ◽  
Wolfram Hoetzenecker ◽  
Manfred Schmidt

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