scholarly journals Large Complex Odontoma of Mandible in a Young Boy: A Rare and Unusual Case Report

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
G. Siva Prasad Reddy ◽  
G. V. Reddy ◽  
B. Sidhartha ◽  
K. Sriharsha ◽  
John Koshy ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
Facial Asymmetry ◽  
Surgical Excision ◽  
Radiographic Examination ◽  
Rare Tumor ◽  
Complex Odontoma ◽  
Compound Odontoma ◽  
Unusual Case Report

Odontomas are the most common odontogenic tumors. They are broadly classified in to Compound Odontoma and Complex Odontoma. Among them complex odontoma is a rare tumor. Occasionally this tumor becomes large, causing expansion of bone followed by facial asymmetry. Otherwise these tumors are asymptomatic and are generally diagnosed on radiographic examination. We report a rare case of complex odontoma of mandible in a young boy. The tumor was treated by surgical excision under general anesthesia.

scholarly journals An Unusual Case Report of Erupted Odontoma

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Dhaval Mehta ◽  
Nilesh Raval ◽  
Sneha Udhani ◽  
Viral Parekh ◽  
Chintan Modi
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Unusual Case ◽  
Tooth Eruption ◽  
Odontogenic Tumors ◽  
Radiographic Examination ◽  
Rare Entity ◽  
Slow Growing ◽  
Compound Odontoma ◽  
Unusual Case Report

Odontomas are the most common of the odontogenic tumors of the jaws, which are benign, slow growing, and nonaggressive. They are usually asymptomatic and found in routine dental radiographic examination. Odontomas are usually associated with tooth eruption disturbances. Eruption of odontoma in oral cavity is rare entity. Here we report a case of an unusual erupted compound odontoma.

scholarly journals Compound odontoma causing impaction of primary tooth in a 4-year-old child: case report

2021 ◽  
Vol 25 (3) ◽  
pp. 348-353
Author(s):  
Sabrina Pozatti Moure ◽  
Natalia Matos Menezes ◽  
Henrique Castilhos Ruschel ◽  
Humberto Thomazi Gassen ◽  
Simone Helena Ferreira
Keyword(s):  
Case Report ◽  
Clinical Management ◽  
Rare Case ◽  
Unusual Case ◽  
Surgical Excision ◽  
Permanent Teeth ◽  
Primary Tooth ◽  
Mandibular Incisor ◽  
Age Range ◽  
Compound Odontoma

Objective: to report a rare case of impaction of a primary mandibular incisor due to the presence of a compound odontoma and describe its clinical management. Case report: a 4-year-old boy presented with a“missing” primary left mandibular lateral incisor. Radiographs showed impaction of the unerupted incisorby adjacent radiopaque structures consistent with a compound odontoma. The patient was recalled periodically for 2 years, at which time surgical excision was performed. The diagnosis of compound odontoma was confirmed histologically, and the permanent mandibular central incisors erupted uneventfully; the patient was referred for orthodontic treatment. Final considerations: this case report describes an unusual case of compound odontoma associated with an unerupted deciduous tooth; odontomas are rare in this age range, occurring predominantly in the second decade of life and in association with impaction of permanent teeth. We also propose a protocol for clinical management of such early-onset cases.

ENTRAPMENT OF THE MEDIAN NERVE BETWEEN SUBLIMIS TENDONS AFTER DISTAL FOREARM FRACTURE: AN UNUSUAL CASE REPORT

Hand Surgery ◽  
2008 ◽  
Vol 13 (02) ◽  
pp. 111-114
Author(s):  
Y. Taniguchi ◽  
T. Kitano ◽  
T. Shimoe ◽  
M. Yoshida
Keyword(s):  
Case Report ◽  
Median Nerve ◽  
Rare Case ◽  
Nerve Palsy ◽  
Unusual Case ◽  
Forearm Fracture ◽  
Distal Forearm ◽  
Distal Forearm Fracture ◽  
Median Nerve Palsy ◽  
Unusual Case Report

We present a rare case of entrapment of the median nerve between sublimis tendons after fractures of the distal radius and ulna in an 80-year-old woman. The entrapped median nerve was elongated redundantly with two regions of constriction. To our knowledge, no case of median nerve palsy caused by such a factor has been previously reported.

Multiple Dentogerous Cysts With a Complex Odontoma: An Unusual Case Report

2015 ◽  
Vol 8 (2) ◽  
pp. 2-2 ◽  
Author(s):  
Mahnaz Sheikhi ◽  
Mohamad Hasan Samandari ◽  
Mitra Karbasi Kheir ◽  
Amir Hosein Moaddabi
Keyword(s):  
Case Report ◽  
Unusual Case ◽  
Complex Odontoma ◽  
Unusual Case Report

scholarly journals Sinonasal Paraganglioma: A Case Report and Review of Literature

2014 ◽  
Vol 7 (2) ◽  
pp. 87-89 ◽  
Author(s):  
Neelam Wadhwa ◽  
PP Singh ◽  
Vipin Arora ◽  
Pankaj Verma ◽  
Khyati Bhatia
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Nasal Cavity ◽  
Rare Case ◽  
Surgical Excision ◽  
Histopathological Diagnosis ◽  
Rare Tumor ◽  
Review Of Literature ◽  
Diagnostic Challenge ◽  
History Of

ABSTRACT A rare case of sinonasal paraganglioma is described. A 40-year-old female patient presented with 2 years history of unilateral nasal obstruction and bleeding. CT scan demonstrated an expansile enhancing mass involving bilateral ethmoids, right nasal cavity and right maxillary sinus. Histopathological diagnosis was neuroendocrine tumor with possibility of paraganglioma. A subtotal maxillectomy with excision of mass performed. Primary nonchromaffin paraganglioma of nose and paranasal sinus is a very rare tumor, these lesion pose diagnostic challenge to clinicians and pathologist. Only twenty five cases are reported in review of literature. Surgical excision is the mainstay of treatment. How to cite this article Arora V, Verma P, Singh PP, Wadhwa N, Bhatia K. Sinonasal Paraganglioma: A Case Report and Review of Literature. Clin Rhinol An Int J 2014;7(2):87-89.

scholarly journals Mixed olfactory neuroblastoma and neuroendocrine carcinoma: An unusual case report and literature review

2020 ◽  
Vol 11 ◽  
pp. 97
Author(s):  
Wilson P. Lao ◽  
Jordan M. Thompson ◽  
Lauran Evans ◽  
Yohanan Kim ◽  
Laura Denham ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Unusual Case ◽  
Olfactory Neuroblastoma ◽  
Pathology Report ◽  
High Grade ◽  
Case Description ◽  
Rare Tumor ◽  
Nasopharyngeal Angiofibroma ◽  
Unusual Case Report

Background: The aim of the study was to present a case of mixed olfactory neuroblastoma (ONB) and carcinoma, an extremely rare tumor with only a few cases in the published literature. Case Description: An otherwise healthy 27-year-old male presented with sinus complaints, headache, and unilateral eye discharge. Imaging and endoscopy revealed a mass presumed to represent a juvenile nasopharyngeal angiofibroma. Unexpectedly, the final pathology report revealed high grade mixed ONB and carcinoma. This tumor is the sixth and youngest documented patient with mixed ONB and carcinoma. Conclusion: Physicians should remain vigilant for the possibility of malignancy in their approach to nasal cavity masses, even in young otherwise healthy patients. Careful review of the immunohistopathology should also be taken, as mixed olfactory tumors such as these are aggressive, rare entities that require multidisciplinary oncologic care.

scholarly journals External angular dermoid cyst: An unusual case report with surgical intervention and clinico-pathological analysis.

2016 ◽  
Vol 19 (4) ◽  
pp. 110
Author(s):  
Pavan Kumar Gujjar ◽  
Treville Pereira ◽  
Jyoti Zingade
Keyword(s):  
Case Report ◽  
Optic Nerve ◽  
Dermoid Cyst ◽  
Unusual Case ◽  
Surgical Intervention ◽  
Neck Region ◽  
Surgical Excision ◽  
Head And Neck Region ◽  
Pathological Analysis ◽  
Unusual Case Report

<p>Dermoid and epidermoid cysts which belong to choristomas, usually manifest clinically as superficial and deep cystic movable formations, most often with a slow and intermittent growth. In the present article we report a case of an external angular dermoid cyst in a 13-year-old boy, the growth of which was steady on progression. Surgical excision of the cyst was done by approaching through an external sub-brow incision. Dermoid cysts are unusual neoplasms that often seen in children with the most commonly affected site being the orbit in the head and neck region. Such cysts may cause compression to the eye lobe and the optic nerve. Hence, operative procedures may be suggested in the case of such cysts which have a constant progression. </p><p>Keywords: Choristoma; Dermoid; Sub-brow incision.</p>

scholarly journals Ruptured anterior communicating artery aneurysm with spontaneous ventriculitis: An unusual case report with review of literature

2017 ◽  
Vol 31 (2) ◽  
pp. 211-214
Author(s):  
Mayank Sinha ◽  
Ashok Gupta ◽  
Amit Pratap Singh Deora ◽  
Mukesh Vij
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Rare Case ◽  
Unusual Case ◽  
Artery Aneurysm ◽  
Anterior Communicating Artery ◽  
Review Of Literature ◽  
Appropriate Treatment ◽  
Life Threatening ◽  
Unusual Case Report

Abstract Ventriculitis is a potentially life-threatening infection, and an early diagnosis is essential for the appropriate treatment of ventriculitis. Unsuspected ventriculitis might be a source of persistent infection and therapeutic failure in the management of meningitis. We present a rare case of spontaneous ventriculitis in a patient of acomm aneurysm who was neither immunocompromised nor any intervention was done on him.

scholarly journals Rare Case of Unerupted Second Deciduous Molar with Congenitally Missing Second Permanent Premolar: Case Report

2020 ◽  
Vol 24 (3) ◽  
pp. 65-67
Author(s):  
Anna Kana ◽  
Tanya Lommerse ◽  
Andrew Birnie
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Unusual Case ◽  
Radiographic Examination ◽  
Supernumerary Teeth ◽  
Deciduous Molar ◽  
Congenitally Missing ◽  
Missing Tooth

SummaryBackground/Aim: The purpose of this report is to present an unusual case of failure of eruption of a second deciduous molar and its management.Case Report: An 8-year-old boy presented with a complaint of a missing tooth. Radiographic examination revealed the second deciduous molar was impacted without any mechanical obstacles, like an odontoma or supernumerary teeth, being present.Conclusions: The case presented in this report is of scientific relevance due to the rarity of this type of pathology and the interesting histopathology.

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