scholarly journals An Aggressive Calcifying Epithelial Odontogenic Tumor: A Rare Case Report

2021 ◽  
pp. 24-30
Author(s):  
Sheetal Singar ◽  
Ajay Pratap Singh Parihar ◽  
Prashanthi Reddy ◽  
Ashish Saxena ◽  
Arvind Jain
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Odontogenic Tumor ◽  
Literature Report ◽  
Calcifying Epithelial Odontogenic Tumor ◽  
Epithelial Origin ◽  
Rare Case Report ◽  
The Face ◽  
Slow Growing ◽  
Epithelial Odontogenic Tumor

Calcifying epithelial odontogenic tumor is an epithelial origin locally aggressive benign odontogenic tumor. It is an extremely rare neoplasm comprise of <1 % of all odontogenic tumors. It manifests clinically as asymptomatic, slow-growing, and locally aggressive lesion which causes expansion of the affected bone. About 400 cases of CEOT (calcifying epithelial odontogenic tumor) are reported in the literature. This article reported a case 18 years old female with a locally aggressive calcifying epithelial odontogenic tumor involving the mandible, without much disfigurement of the face. Aim: The aim of this article to put a drop of water in the ocean of literature. Report a case with aggressive nature.

scholarly journals Gingival Calcifying Epithelial Tumor - A Rare Case Report

2015 ◽  
Vol 12 (3) ◽  
pp. 215-218
Author(s):  
MLA Tejasvi ◽  
BB Bangi ◽  
P Geetha ◽  
D Pavani ◽  
B Harsha
Keyword(s):  
Rare Case ◽  
Case Reports ◽  
English Literature ◽  
Odontogenic Tumor ◽  
Odontogenic Tumors ◽  
Epithelial Tumor ◽  
Calcifying Epithelial Odontogenic Tumor ◽  
Rare Case Report ◽  
Pubmed Search ◽  
Epithelial Odontogenic Tumor

Calcifying epithelial odontogenic tumors are rare odontogenic neoplasms that account for approximately one percent of all odontogenic tumors. Extra osseous variant is very rare with very few cases being reported in literature Peripheral Calcifying epithelial odontogenic tumor (CEOT) commonly resemble oral hyperplastic or reactive lesions and are histologically similar to their intraosseous counterparts. Here we report a rare case of gingival calcifying epithelial odontogenic tumor in the mandibular posterior region in a 31 year old female patient. Interestingly on literature review in on PubMed search only 22 case reports were available in, English literature, added to that this report will be the 23rd case.Kathmandu University Medical Journal Vol.12(3) 2014; 215-218

scholarly journals Bilateral Sturge Weber Syndrome- a rare case report

2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
The Other ◽  
Advanced Stage ◽  
Weber Syndrome ◽  
Rare Case Report ◽  
The Face ◽  
Bilateral Condition ◽  
Sturge Weber Syndrome

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841

Clear cell variant of calcifying epithelial odontogenic tumor: Case report and review of the literature

Head & Neck ◽  
1994 ◽  
Vol 16 (3) ◽  
pp. 272-277 ◽  
Author(s):  
M. John Hicks ◽  
Catherine M. Flaitz ◽  
Mark E. K. Wong ◽  
R. Keith McDaniel ◽  
Philip T. Cagle
Keyword(s):  
Case Report ◽  
Clear Cell ◽  
Odontogenic Tumor ◽  
Review Of The Literature ◽  
Calcifying Epithelial Odontogenic Tumor ◽  
Cell Variant ◽  
Clear Cell Variant ◽  
Epithelial Odontogenic Tumor

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.

scholarly journals Psoriasiform Mycosis Fungoides Involving the Face- A Rare Case Report

2021 ◽  
pp. 94-99
Author(s):  
N. R. Vignesh ◽  
Shreya Srinivasan ◽  
G. Sukanya ◽  
S. Arun Karthikeyan
Keyword(s):  
Case Report ◽  
Mycosis Fungoides ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Punch Biopsy ◽  
Cutaneous T Cell Lymphoma ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Atypical Cells ◽  
The Face

Mycosis fungoides is represented as the most common epidermotropic cutaneous T-cell lymphoma, which is mainly characterized by the proliferation of atypical cells within the epidermis. We report a rare presentation of mycosis fungoides in a 60-year-old male presenting with chronic psoriasiform plaque involving the face. Punch biopsy of the lesion from the forehead was taken for routine histological examination and immunohistochemical stains. Results of biopsy and immunohistochemical findings were consistent with mycosis fungoides and diagnosed as psoriasiform presentation of mycosis fungoides involving the face.

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