scholarly journals Binder's Syndrome – A Rare Case Report and Review of Literature with detailed treatment Plan

2016 ◽  
Vol 9 (3) ◽  
pp. 1049-1055
Author(s):  
ALAGARSAMY VENKATESH ◽  
B. ANURADHA ◽  
A. KARTHICK ◽  
P. E. CHANDRA MOULI ◽  
M. RAMASAMY
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Treatment Plan ◽  
Review Of Literature ◽  
Detailed Treatment ◽  
Rare Case Report

scholarly journals A Review of Literature on Ameloblastoma in Children and Adolescents and a Rare Case Report of Ameloblastoma in a 3-Year-Old Child

2012 ◽  
Vol 5 (3) ◽  
pp. 161-168 ◽  
Author(s):  
Zainab Chaudhary ◽  
Sriram Krishnan ◽  
Pankaj Sharma ◽  
Rakesh Sharma ◽  
Priya Kumar
Keyword(s):  
Case Report ◽  
Children And Adolescents ◽  
Rare Case ◽  
Treatment Plan ◽  
Incidence Rates ◽  
Review Of Literature ◽  
Hand Search ◽  
Medline Search ◽  
Unicystic Ameloblastoma ◽  
Rare Case Report

A rare case report of a plexiform unicystic ameloblastoma in a 3-year-old girl stimulated us to conduct a review of literature to understand the correlation of this tumor with various factors such as that of age, sex, histopathological correlation, and its incidence rates pertaining to children and adolescent population. This is a case report of ameloblastoma in a 3-year-old patient, along with a literature review of ameloblastoma in relation to age. A computerized literature search using Medline was conducted for published articles on treatment of ameloblastoma. MeSH phrases used in search were ameloblastoma AND age; ameloblastoma AND children. The search was restricted to published articles from 1970 to 2010, as the histological features were not clearly defined until 1st edition of WHO histological classification of odontogenic tumors of 1971, search parameter was also set to select literatures under English language only. An additional systematic hand search was also conducted simultaneously to identify other published articles, considering similar parameters as used for Medline search. Most of search result yielded literatures in which primary importance were given to treatment patterns and prognosis of intervention, there were not much specific article or meta analysis which reviewed on the affected age range of ameloblastoma exclusively. We reviewed the identified literatures with patients’ age, case numbers, incidence, sex, location, and histopathology. The statistical data collected were exported to SPSS 16.0 for windows software which performed a descriptive analysis giving an average mean age of 14.1 years (range from 4 to 20); with maximum mean age being 16.0 and minimum mean age being 10.8 with standard deviation of 1.60. Majority of lesions 91.86% (327 of 356) were found between the age group of 11 and 20 years, only 8.14% (29 of 356) were below the age of 10 years. This rare case report highlights occurrence of plexiform unicystic ameloblastoma in maxilla of a 3-year-old girl, which is very much incongruent with the various review of literature on ameloblastoma in children and adolescents. We have emphasized the significance of patient's age and histopathological pattern of the tumor as it has its influence on the treatment plan. However, there is much of research needed with focus in respect to age, histological pattern, and treatment outcomes.

Intraosseous Neurofibroma of Mandible in a 5-Year-Old: A Rare Case Report and Review of Literature

2021 ◽  
Author(s):  
Arunkumar Kamalakaran ◽  
Balaji Jayaraman ◽  
Supraja Raghavendran ◽  
Rohini Thirunavukkarasu ◽  
Mariammal Ayyappan ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Rare Case Report

scholarly journals The subdural extramedullary angiolipoma: A rare case report and review of literature

2016 ◽  
Vol 4 (1) ◽  
Author(s):  
Yue-hua Lyu ◽  
Zong-hui Liang ◽  
Yu-lin Xi ◽  
Hua-li Zhao
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Rare Case Report

scholarly journals Primary bone lymphoma with multifocal osteolytic lesions: a rare case report with review of literature

2015 ◽  
Vol 50 (4) ◽  
pp. 256 ◽  
Author(s):  
Prakas Kumar Mandal ◽  
Shuvraneel Baul ◽  
Tuphan Kanti Dolai
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Osteolytic Lesions ◽  
Primary Bone Lymphoma ◽  
Rare Case Report ◽  
Primary Bone ◽  
Bone Lymphoma

scholarly journals Agenesis of Bilateral Permanent Mandibular Canine: A Rare Case Report

2016 ◽  
Vol 04 (01) ◽  
pp. 056-058
Author(s):  
Deepti Jindal ◽  
Varun Jindal ◽  
Himanshu Singh ◽  
Swati Gautam ◽  
Ishita Bhojia ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Congenital Absence ◽  
Dental Arch ◽  
Review Of Literature ◽  
Third Molars ◽  
Comprehensive Review ◽  
Rare Case Report ◽  
Mandibular Canine ◽  
Congenitally Missing

AbstractHypodontia is the congenital absence of less than six teeth because of agenesis. Congenital absence of tooth (hypodontia) from the dental arch, may occur with any tooth, most commonly being third molars, however, absence of permanent mandibular canine is rare. The absence of teeth may be unilateral or bilateral. There are reports showing unilateral occurrence of permanent mandibular canines but agenesis of bilateral mandibular canines is not well documented in the literature and comprehensive review of literature shows paucity of data pertaining to this anomaly. Here we report one such rare case of congenitally missing mandibular permanent canines bilaterally.

scholarly journals Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature

2015 ◽  
Vol 6 (3) ◽  
pp. 115-117
Author(s):  
Sachin Lal Shilpakar ◽  
Bivek Aryal ◽  
Shyam Thapa Chettri ◽  
Apar Pokharel ◽  
Deepak Paudel
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histopathological Examination ◽  
Hair Follicles ◽  
Review Of Literature ◽  
Solitary Lesion ◽  
Biological Potential ◽  
Rare Case Report ◽  
The Face ◽  
Head Neck

ABSTRACT The trichoepithelioma is a benign cutaneous neoplasm which is derived from hair follicles. It is common in the face, but there are only three reports of the solitary occurrence on the nose. It is often not recognized because of its rarity, controversial classification, origin and biological potential. The objective of this paper is to present a case of solitary trichoepithelioma on the nose, histopathological examination and treatment. It should be considered as a differential diagnosis of a solitary lesion of nose which is confused with basal cell carcinoma. The confirmation by histopathological examination is essential. How to cite this article Sah BP, Shilpakar SL, Aryal B, Chettri ST, Pokharel A, Mishra S, Paudel D. Solitary Trichoepithelioma of Nose: A Rare Case Report and Review of Literature. Int J Head Neck Surg 2015;6(3):115-117.

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