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.

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 Treatment of a Patient with Multiple Impacted Teeth

2007 ◽  
Vol 77 (4) ◽  
pp. 735-741 ◽  
Author(s):  
Richard Scott Conley ◽  
Scott B. Boyd ◽  
Harry L. Legan ◽  
Christopher C. Jernigan ◽  
Craig Starling ◽  
...  
Keyword(s):  
Case Report ◽  
Treatment Planning ◽  
Orthodontic Treatment ◽  
Primary Teeth ◽  
Permanent Tooth ◽  
Permanent Teeth ◽  
Treatment Sequence ◽  
Impacted Teeth ◽  
Case Complexity ◽  
Multiple Primary

Abstract An impacted or missing permanent tooth can add significant complications to an otherwise straightforward case. When multiple impacted teeth are present, the case complexity increases further. Developing a treatment sequence, determining appropriate anchorage, and planning and executing sound biomechanics can be a challenge. The following case report illustrates a patient reportedly diagnosed with mild scleroderma as an adolescent. He presented for orthodontic treatment as an adult with multiple retained primary teeth and multiple impacted teeth. Diagnosis, treatment planning, and various methods of managing guided eruption of impacted teeth will be discussed. Following orthodontic treatment that required extraction of multiple primary and permanent teeth as well as exposure and ligation of multiple permanent teeth by an oral surgeon, the patient finished with a significantly improved functional and esthetic result.

Aggressive periodontitis of the primary dentition associated with idiopathic immune deficiency: case report and treatment considerations

2005 ◽  
Vol 29 (1) ◽  
pp. 27-31 ◽  
Author(s):  
Enrique Bimstein ◽  
Michael McIlwain ◽  
Joseph Katz ◽  
Greg Jerrell ◽  
Robert Primosch
Keyword(s):  
Immune Deficiency ◽  
Case Report ◽  
Primary Teeth ◽  
Aggressive Periodontitis ◽  
Primary Dentition ◽  
Permanent Teeth ◽  
Gingival Inflammation ◽  
Adequate Treatment ◽  
Treatment Considerations ◽  
Topical Applications

The present case, of a child with an idiopathic immune deficiency and aggressive periodontitis in the primary dentition, serves as an example for the treatment considerations in these cases. Extraction of all the primary teeth proved to be the most adequate treatment. It allowed the child to eat properly and prevented unwanted infections that could endanger the life of the child. The newly erupted permanent teeth have been subjected to careful oral hygiene, clorhexidine topical applications, and have mild gingival inflammation and no attachment loss.

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 Natal and Neonatal Teeth: A Case Report and Mecanistical Perspective

Healthcare ◽  
2020 ◽  
Vol 8 (4) ◽  
pp. 539
Author(s):  
Emil Anton ◽  
Bogdan Doroftei ◽  
Delia Grab ◽  
Norina Forna ◽  
Mihoko Tomida ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Condition ◽  
Radiographic Examination ◽  
Adequate Treatment ◽  
Dental Papilla ◽  
Ongoing Development ◽  
Risk Of Aspiration ◽  
The Relationship ◽  
Dental Papilla Cells

The presence of teeth on babies earlier than four months is a rare condition. Therefore, adequate treatment for each case should be instituted as soon as possible, considering that certain complications may arise. This report describes a rare case in which a newborn baby required the extraction of two mobile mandibular natal teeth to prevent the risk of aspiration. After two years, the clinical re-evaluation showed a residual tooth instead of a temporary one. This case report shows that adequate diagnosis should include a radiographic examination to determine whether these teeth are components of normal or supernumerary dentition, as well as further investigations on the relationship with the adjacent teeth. Another important aspect highlighted in this case report is the need for a post-extraction curettage of the socket in order to reduce the risk of ongoing development of the dental papilla cells.

scholarly journals Intersphincteric epidermoid inclusion cyst: report of a rare case

2020 ◽  
Vol 2020 (3) ◽  
Author(s):  
James Ashcroft ◽  
Betania Mahler-Araujo ◽  
Richard J Davies
Keyword(s):  
Case Report ◽  
Surgical Technique ◽  
Rare Case ◽  
Unusual Case ◽  
Accurate Diagnosis ◽  
Rare Entity ◽  
Inclusion Cyst ◽  
Patient Morbidity ◽  
Perineal Region ◽  
Epidermoid Inclusion Cyst

Abstract Epidermoid inclusion cysts of the perineal region are a rare entity, which require appropriate diagnosis and management. Here we describe the unusual case of a large protruding epidermoid inclusion cyst originating from the intersphincteric anal plane, which was mobilized and excised successfully. Essential investigations to ensure accurate diagnosis in addition to surgical technique to reduce recurrence and patient morbidity are described in this case report.

An Unusual Case of an Odontogenic Keratocyst Associated With an Ungrafted Alveolar Cleft: A Case Report and Review of the Literature

2018 ◽  
Vol 56 (1) ◽  
pp. 110-115 ◽  
Author(s):  
Sapna Radia ◽  
Alexander C. Cash ◽  
Kanwalraj Moar
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Bone Grafting ◽  
Unusual Case ◽  
Odontogenic Keratocyst ◽  
Permanent Teeth ◽  
Treatment Modalities ◽  
Review Of The Literature ◽  
Alveolar Cleft

We describe an unusual case of an odontogenic keratocyst (OKC) associated with an ungrafted left-sided alveolar cleft in a 10-year-old male patient. There is no previous report in the literature of OKC or other dental cysts associated with an alveolar cleft. We discuss the management of the OKC prior to secondary bone grafting and present this case to highlight the difficulty in the management of OKC concurrent with grafting of the alveolar cleft site, the proximity of unerupted permanent teeth, and possible treatment modalities.

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