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.

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 Nonsyndromic Familial Oligodontia with Multiple Dens Invaginatus: A Case Report of an Unusual Case

2013 ◽  
Vol 2013 ◽  
pp. 1-6
Author(s):  
D. P. Vinuth ◽  
Poonam Agarwal ◽  
Gunjan Dube ◽  
S. Abhilash ◽  
Pallavi Dube
Keyword(s):  
Case Report ◽  
Treatment Planning ◽  
Rare Case ◽  
Unusual Case ◽  
Early Recognition ◽  
Permanent Teeth ◽  
Adequate Treatment ◽  
Growth Disturbances ◽  
Evolutionary Genetic ◽  
Dens Invaginatus

Oligodontia is a rare dental anomaly with a prevalence of 0.3% in permanent teeth and much less frequency in the primary dentition. Familial oligodontia represents an absence of varying numbers of primary and/or secondary teeth as an isolated trait. It is a complex and multifactorial condition. Many explanations—evolutionary, genetic, and environmental—have been proposed as the etiology. Simultaneous with oligodontia are often the different positional changes of the existing teeth, their morphology, size, and growth disturbances of the maxillofacial skeleton. Early recognition is vital to provide adequate treatment and prevent squeal. Multidisciplinary referral or consultation is thus important in treatment planning to improve function and esthetics. The present paper reports a rare case of familial oligodontia associated with multiple dense invaginatus and microdontia.

Compound odontoma in a nine-year-old boy associated with impacted permanent central and lateral incisor — a case report

2020 ◽  
pp. 1-8
Author(s):  
Abul khair Zalan ◽  
Anser Maxood ◽  
Palwasha Baber ◽  
Anika Gul ◽  
Hira Nisar ◽  
...  
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Primary Teeth ◽  
Surgical Excision ◽  
Genetic Mutation ◽  
Permanent Teeth ◽  
Central Incisor ◽  
Odontogenic Origin ◽  
Delayed Eruption ◽  
Compound Odontoma

Abstract Odontomas are one of the most common tumours of odontogenic origin. They are usually asymptomatic but may be associated with retained primary teeth or missing permanent teeth. Though the exact aetiology is unknown, the postulated causes include trauma, infection, inheritance and genetic mutation. Early diagnosis and management will result in fewer complications. Conservative surgical excision is the treatment of choice. This case report presents a treated case of compound odontoma associated with delayed eruption of the permanent central incisor in a nine-year-old boy. Keywords: Compound Odontoma. Continuous...

scholarly journals Evolution of superficial spreading melanoma to resemble desmoplastic melanoma: case report

2021 ◽  
Author(s):  
Martin G. Cook ◽  
Barry W. E. M. Powell ◽  
Megan E. Grant ◽  
Adele C. Green
Keyword(s):  
Case Report ◽  
Clinical Management ◽  
Unusual Case ◽  
Primary Site ◽  
Mixed Tumor ◽  
Superficial Spreading ◽  
Superficial Spreading Melanoma ◽  
Desmoplastic Melanoma ◽  
Mixed Features ◽  
Melanoma Case

AbstractDesmoplastic melanoma commonly occurs on the head and neck in a pure form, but occasionally, it occurs in a mixed tumor with another type, usually superficial spreading melanoma (SSM), and rarely as a metastasis from a primary SSM. We report here a primary SSM on the leg of a 32-year-old male which metastasised to lymph nodes, and 10 years later recurred at the primary site initially with mixed features but evolving to resemble a uniformly desmoplastic, deeply invasive melanoma. This unusual case has implications for clinical management and is additionally notable for its reversal in behavior, from metastatic to local infiltrative type, correlating with the change in morphology.

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

scholarly journals Idiopathic multiple unerupted permanent teeth: A rare case report

2014 ◽  
Vol 3 (4) ◽  
pp. 283 ◽  
Author(s):  
Sandra Vani ◽  
Anitha Nooney ◽  
KakarlaSubba Raju ◽  
Melpati Hemadri
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Permanent Teeth ◽  
Rare Case Report

scholarly journals Facial talon cusp on mandibular incisor: A rare case report with review of literature

2014 ◽  
Vol 25 (3) ◽  
pp. 398 ◽  
Author(s):  
SureshK Sachdeva ◽  
Pradhuman Verma ◽  
Sanjay Dutta ◽  
KanikaGupta Verma
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Review Of Literature ◽  
Mandibular Incisor ◽  
Rare Case Report

scholarly journals Cerebral Coenurosis Masquerading as Malignancy: A Rare Case Report from India

2019 ◽  
Vol 10 (02) ◽  
pp. 367-370
Author(s):  
Shamila Mohamed Ali ◽  
P. Somashekara Reddy ◽  
S. Venugopal ◽  
Manmeet Chhabra ◽  
Anita Mahadevan
Keyword(s):  
Case Report ◽  
Characteristic Feature ◽  
Rare Case ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Hydatid Cysts ◽  
The Third ◽  
Rare Case Report ◽  
Cerebral Coenurosis ◽  
Cuticular Layer

ABSTRACTHuman coenurosis is a rare zoonotic disease caused by the larvae of Tinea multiceps seen in sheep-rearing countries. We report the case of a 63-year-old male who was referred to our hospital with a working diagnosis of skull base chondrosarcoma. Histopathological examination after surgical excision revealed characteristic feature of coenurus with multiple scolices invaginating from the outer cuticular layer. Coenuri are often mistaken for giant cysticercal cysts and hydatid cysts. Despite its wide prevalence in cattle, only two cases of human coenurosis are reported from India till date. We report the third case from India.

scholarly journals Scrotal lymphangiomatosis: a case report

2013 ◽  
Vol 6 (1) ◽  
pp. 11 ◽  
Author(s):  
Rachel Wong ◽  
Megan Melnyk ◽  
Steven S. Tang ◽  
Chris Nguan
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Lymphatic System ◽  
Surgical Excision ◽  
Skin Grafts ◽  
Thickness Skin ◽  
Benign Tumours

Lymphangiomas are benign tumours of the lymphatic system, andthere are several reported cases of scrotal lymphangioma in theliterature to date. We report a rare case of multilocular cutaneouslymphangiomatosis treated with surgical excision (total scrotectomyand reconstruction using split-thickness skin grafts withvacuum-assisted closure dressing).

scholarly journals LIPOSARCOMA OF SPERMATIC CORD PRESENTING AS INDIRECT INGUINAL HERNIA- A RARE CASE REPORT

2011 ◽  
Vol 01 (01/03) ◽  
pp. 63-65
Author(s):  
Padma Shetty K. ◽  
Harish S. Permi ◽  
Michelle Mathias ◽  
Kishan Prasad ◽  
Teerthanath S. ◽  
...  
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Spermatic Cord ◽  
Rare Case ◽  
Surgical Excision ◽  
Myxoid Liposarcoma ◽  
Clinical Findings ◽  
Inguinal Region ◽  
Indirect Inguinal Hernia ◽  
Rare Case Report

AbstractLiposarcoma in the inguinal region though rare are clinically significant lesions. Preoperative diagnosis is difficult since the clinical findings are very similar to that of inguinal hernia. We report a rare case of Liposarcoma of the spermatic cord in 85 year old male, clinically diagnosed as left sided indirect inguinal hernia. Surgical excision specimen showed multiple globular lipomatous masses which were yellowish and grey tan with areas of myxoid degeneration and necrosis seen. Microscopic examination showed adipocytes arranged in lobules with numerous blood vessels, lipoblasts and myxoid stroma confirming the diagnosis of myxoid liposarcoma. He is on regular follow up since two years without any recurrence or metastasis. Our case report highlights the importance of sampling and examination of fatty masses in the inguinal region to rule out the possibility of liposarcoma as they are mistaken for lipoma at surgery.

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