scholarly journals Keratocystic odontogenic tumor involving the maxillary antrum with displacement of the third molar: A rare case report

2014 ◽  
Vol 26 (3) ◽  
pp. 335
Author(s):  
RashmiShivakumar Doshetty ◽  
AshwiniKumar Mengji ◽  
UdayShankar Yaga ◽  
Radhika Besta
2013 ◽  
Vol 4 (3) ◽  
pp. 132
Author(s):  
RiteshR Kalaskar ◽  
AshitaR Kalaskar ◽  
ChetanA Pol ◽  
SuvarnaK Ghige

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.


2013 ◽  
Vol 14 (1) ◽  
pp. 133-136 ◽  
Author(s):  
Poorandokht Davoodi ◽  
Loghman Rezaei-Soufi ◽  
Mina Jazaeri ◽  
Adineh Javadian Langaroodi ◽  
Seyed Hossein Hoseini Zarch

ABSTRACT Aim The aim of this report is to introduce a rare case in which an infected keratocystic odontogenic tumor (KCOT) was initially diagnosed and treated as a dentoalveolar abscess. Background Keratocystic odontogenic tumor (KCOT) is a benign neoplasm that can be secondarily infected. However, cervical soft tissue abscess formation as a result of an infected odontogenic cyst or tumor is a rare condition few of which have only been described in the existing literature. Also, there has been a single report regarding the coincidence of a traumatic bone cyst and a keratocytic odontogenic tumor to date. Case report The patient was a 29-year-old male, complaining of fever, pain and swelling in the left submandibular region. The panoramic radiography showed a well-defined and partially corticated radiolucency between the roots of the second and third left mandibular molars. In addition, a well-corticated radiolucent lesion was incidentally found on the right side of the mandible, which, following surgical exploration, was diagnosed as a traumatic bone cyst. Conclusion In the present report, an infected KCOT manifested as a cervical abscess, coincided with a traumatic bone cyst. Clinical significance From the clinical point of view, it is of paramount significance to prevent misdiagnosis of similar presentations as pulp and periapical lesions, which may lead to mistreatment and thus complications. How to cite this article Davoodi P, Rezaei-Soufi L, Jazaeri M, Javadian Langaroodi A, Hoseini Zarch SH. Submandibular Abscess due to an Infected Keratocystic Odontogenic Tumor associated with Simultaneous Occurrence of a Traumatic Bone Cyst: A Rare Case Report. J Contemp Dent Pract 2013;14(1): 133-136.


2013 ◽  
Vol 14 (2) ◽  
pp. 355-359 ◽  
Author(s):  
C Prashanthi ◽  
Vinayak Karun ◽  
Mahesh Melkundi ◽  
Sanjay Nyamati ◽  
Annapoorna HB

ABSTRACT Aim and background An odontogenic keratocyst (OKC) or keratocystic odontogenic tumor (KCOT) and giant cell granuloma (GCG) in the jaws are common lesions which have been studied extensively in detail over the years. However, a lesion showing features of both is exceptionally rare and is reported only twice in the literature till date. Case description A rare case of OKC in mandible showing foci of GCG like areas is reported in a 29 years old male patient. Conclusion It seems to be a collision lesion, though the possibility of KCOT showing a reactive response to form giant cells or it being a rare variant cannot be totally ruled out. Clinical significance This entity requires aggressive treatment since biological behavior of this unique lesion is difficult to predict unless more of such lesions are reported and followed up in future. How to cite this article Ravi SB, Prashanthi C, Karun V, Melkundi M, Nyamati S, Annapoorna HB. Collision Lesion of Mandible: Coexistence of Keratocystic Odontogenic Tumor with Central Giant Cell Granuloma: A Rare Case Report. J Contemp Dent Pract 2013;14(2):355-359.


2016 ◽  
Vol 10 (02) ◽  
pp. 277-280 ◽  
Author(s):  
Vikas Dhupar ◽  
Francis Akkara ◽  
Pulkit Khandelwal

ABSTRACTAdenomatoid odontogenic tumor (AOT) is a rare tumor comprising only 3% of all odontogenic tumors. It is a benign, encapsulated, noninvasive, nonaggressive, slowly growing odontogenic lesion associated with an impacted tooth. These lesions may go unnoticed for years. The usual treatment is enucleation and curettage, and the lesion does not recur. Here, we present a rare case of an unusually large aggressive AOT of maxilla associated with impacted third molar. The authors also discuss clinical, radiographic, histopathologic, and therapeutic features of the case. Subtotal maxillectomy with simultaneous reconstruction of the surgical defect with temporalis myofascial flap was planned and carried out.


2012 ◽  
Vol 3 (1) ◽  
pp. 100-108 ◽  
Author(s):  
A Nagaraja ◽  
Praveen S Anigol ◽  
Venkatesh Vishwanath Kamath ◽  
Krishnanand P Setlur

ABSTRACT The odontogenic keratocyst (OKC) has recently been reclassified by the WHO (2005), as keratocystic odontogenic tumor (KCOT) based on clinical, histological and immunohistochemical parameters. KCOT more commonly occurs in the mandible and cases involving the maxilla are infrequent. We report an unusual and rare case of a KCOT of the maxilla in a middle-aged individual with extensive involvement and displacement of the maxillary third molar to the zygomatic region. A discussion of the parameters involved in the reclassification of the lesion as a tumor is presented alongwith a review of literature. How to cite this article Nagraja A, Anigol PS, Kamath VV, Setlur KP. Keratocystic Odontogenic Tumor of the Maxilla: Report of a Rare Case and Review of Literature. World J Dent 2012;3(1):100-108.


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