Unilateral double maxillary paramolars in a non-syndromic child – a rare case report

Sonu Acharya
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Bismay Singh
Alkananda Sahoo
Brinda Suhas Godhi
Department of Pediatric and Preventive Dentistry, Institute of Dental Sciences, SOA (Deemed to be University), Bhubaneswar, Odisha, India
Department of Pediatric and Preventive Dentistry, Institute of Dental Sciences, SOA (Deemed to be University), Bhubaneswar, Odisha, India
Department of Oral Pathology and Microbiology, Institute of Dental Sciences, SOA (Deemed to be University), Bhubaneswar, Odisha, India
Department of Pediatric and Preventive Dentistry, JSS Dental College and Hospital, JSS Academy of Higher Education and Research, Mysuru, Karnataka, India
Received: 27 March 2023 / Revised: 3 May 2023 / Accepted: 6 May 2023 / Published: 30 September 2023

Abstract

Introduction and aim. Extra teeth are the teeth which are more than the normal number of teeth in jaws. They can be present on a single side or both sides, singular or many, maxillary or mandibular. Paramolars are uncommon supernumerary molars which can be present on buccal or palatal side of molars. Very few reports of supernumerary teeth in maxilla or mandible being paramolars has been stated. No literature on unilateral twin paramolars in maxilla has been reported in literature yet. This is a first case report of unilateral twin paramolars in maxilla in a child.

Description of the case. This case report describes the presence of unilateral double maxillary paramolars and their handling in a thirteen-year-old boy, whose primary concern was that of severe pain in maxilla on both sides. After an identification of double maxillary paramolars was put forward and established by cone beam computer tomography, both the paramolars were extracted.

Conclusion. Supernumerary teeth have to be removed as soon as detected otherwise they can lead to malocclusion and pain due to caries after pulp involvement.

 

Cite

Acharya S, Singh B, Sahoo A, Godhi BS. Unilateral double maxillary paramolars in a non-syndromic child – a rare case report. Eur J Clin Exp Med. 2023;21(3):654–658. doi: 10.15584/ejcem.2023.3.7.

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