scholarly journals Giant Frontoethmoidal osteoma with orbital involvementa rare case report with review of literature

2017 ◽  
Vol 31 (4) ◽  
pp. 540-544
Author(s):  
Pankaj Gupta ◽  
Arvind Sharma ◽  
Jitendra Singh ◽  
Tarun Ojha
Keyword(s):  
Case Report ◽  
Eye Movement ◽  
Surgical Approach ◽  
Paranasal Sinuses ◽  
Rare Case ◽  
Surgical Intervention ◽  
Review Of Literature ◽  
Rare Case Report ◽  
Benign Tumours ◽  
Open Surgical Approach

Abstract Osteomas are benign tumours that involve paranasal sinuses more than other parts of body. Frontal sinus is most common while sphenoid is least one. They are usually asymptomatic and diagnosed incidentally on imaging for other reasons. Giant variety of frontoethmoid osteoma is very rare and only few cases are described in literature. Orbital involvement in giant frontoethmoid osteoma is even rarer. Due to threat to vision, this variety is an indication for surgical intervention followed by reconstruction of defect. As these tumours are very large, endoscopic approaches are less indicated and there is no clear consensus which open surgical approach is better. We are reporting such a rare case of giant frontoethmoid osteoma causing proptosis and restriction of eye movement that was treated with open surgical approach.

scholarly journals A giant renal angiomyolipoma: a rare case report and review of literature

2021 ◽  
Vol 9 (1) ◽  
pp. 221
Author(s):  
Girish D. Bakhshi ◽  
Rajalakshmi Venkateswaran ◽  
Aishwarya Sunil Dutt ◽  
Sushrut Baligar ◽  
Madhu Jha
Keyword(s):  
Case Report ◽  
Radical Nephrectomy ◽  
Rare Case ◽  
Clinical Presentation ◽  
Review Literature ◽  
Renal Angiomyolipoma ◽  
Review Of Literature ◽  
Good Imaging ◽  
Rare Case Report ◽  
Benign Tumours

Renal angiomyolipomas (AMLs) are the most common benign tumours of the kidney that occur sporadically in 80% of the patients and are seen associated with genetic conditions such as tuberous sclerosis in rest of the patients. The diagnosis of renal AML pre-operatively have been made easier with the advent of good imaging modalities. The management of these tumours depends on factors such as size, clinical presentation, extent of parenchymal involvement and ranges from a wait and watch strategy to a radical nephrectomy. Herewith, we reported of a giant renal AML who presented with complaints of lump in abdomen with headache and palpitations. She was diagnosed to have a giant renal AML on imaging. The patient was managed with radical nephrectomy after renal AML. A brief case report with review literature was presented here.

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 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.

Sign in / Sign up

Export Citation Format

Share Document