Surgical treatment of multiple impacted supernumerary teeth in a cleidocranial dysplasia patient: a case report

Oral Surgery ◽  
2021 ◽  
Author(s):  
Ye Wu ◽  
Shaohai He
2020 ◽  
Vol 9 (9) ◽  
pp. e916998052
Author(s):  
Eleonor Álvaro Garbin Júnior ◽  
Anna Carolina Jaccottet Oliveira ◽  
Niviane Dorigan Vidor ◽  
Mauro Carlos Agner Busato ◽  
Geraldo Luiz Griza ◽  
...  

Cleidocranial dysplasia (CCD) is a rare syndrome, occurring at a rate of 1:10,000,000 in the form presented in this clinical case. This syndrome occurs due to an autosomal dominant inheritance characterized by changes in skeletal formation and development, as a result of a mutation associated with the RUNX2 gene, the main regulatory gene for osteoblastic differentiation, resulting in manifestations such as hypoplastic or aplastic clavicles, brachycephaly, hypoplasia of the middle third of the face, and delay or non-closure of fontanelles. Specifically, in the intraoral region, atypical dental manifestations occur, such as failure in the exfoliation of the primary dentition, delayed eruption of permanent teeth, and multiple supernumerary teeth. Thus, this study aims to present a case report of a patient with the pathognomonic characteristics of the syndrome in its rarest form, as well as the radiographic, imaging and clinical manifestations that allow its diagnosis and a discussion on the common manifestations in such patients, forms of treatment, and the conduct of treatment according to the specific needs of that case..


1970 ◽  
Vol 21 (2) ◽  
pp. 166-169
Author(s):  
M Azizul Haque ◽  
ARM Saifuddin Ekram ◽  
M Durrul Huda

Cleidocranial dysplasia is an autosomal dominant disorder with a wide range of expression, characterized by clavicular aplasia or hypoplasia, retarded cranial ossification, supernumerary teeth, short stature and a variety of other skeletal abnormalities. We are reporting a case of Cleidocranial dysplasia with literature is review. doi: 10.3329/taj.v21i2.3799   TAJ 2008; 21(2): 166-169   


2020 ◽  
Vol 9 (6) ◽  
pp. 553-556
Author(s):  
Vítor Bruno Teslenco ◽  
Maylson Alves Nogueira Barros ◽  
Everton Floriano Pancini ◽  
Herbert de Abreu Cavalcanti ◽  
Guilherme Nucci dos Reis

Introdução: Anomalias de forma, tamanho, formato, número, estrutura, e erupção dentária são comumente vistas dentro da odontologia. Dentre elas temos a hiperdontia ou dentes suprenumerários. A etiologia desta patologia não foi realmente esclarecida, porém estas anormalidades são gerenciadas por um complexo sistema de interação genética e ambiental. Objetivo: relatar à comunidade científica um caso diagnosticado como displasia cleidocraniana, onde foram removidos 34 dentes supranumerários de uma paciente. Relato de caso: Paciente do gênero feminino, 12 anos de idade, diagnosticada com displasia cleidocranina. Foram realizados um total de 04 procedimentos, para remoção dos dentes e tracionamento dos permanentes impactados. Todos os procedimentos foram realizados sob anestesia local. Conclusão: O principal fator a se considerar para que busquemos o sucesso no tratamento destes pacientes é o diagnóstico precoce. Desta maneira, podemos buscar de maneira multidisciplinar um adequado plano de tratamento, evitando complicações futuras ao paciente portador da síndrome. Descritores: Dente Impactado; Dente Supranumerário; Cirurgia Bucal; Displasia Cleidocraniana. Referências Hattab FN, Yassin OM, Rawashdeh MA. Supernumerary teeth: report of three cases and review of the literature. ASDC J Dent Child. 1994;61(5-6):382-93.  Scheiner MA, Sampson WJ. Supernumerary teeth: a review of the literature and four case reports. Aust Dent J. 1997;42(3):160-65.  Teslenco VB, Gaetti ECJ, Silva JCL. Bilateral supernumerary mandibular: case report. Arch Health Invest. 2017;6(3):110-14. Neville BW, Damm DD, Alen CM, Bouquot JE. Patologia oral e maxilofacial. 4.ed. Rio de Janeiro: Elsevier; 2016. Garvey MT, Barry HJ, Blake M. Supernumerary teeth--an overview of classification, diagnosis and management. J Can Dent Assoc. 1999;65(11):612-16. Mundlos S. Cleidocranial dysplasia: clinical and molecular genetics. J Med Genet. 1999; 36(3):177-82. Kreiborg S, Jensen BL. Tooth formation and eruption - lessons learnt from cleidocranial Eur J Oral Sci. 2018;126(Suppl 1):72-80. Ma Y, Zhao F, Yu D. Cleidocranial dysplasia syndrome with epilepsy: a case report. BMC Pediatr. 2019;19(1):97.


2014 ◽  
Vol 25 (1) ◽  
pp. 79-82
Author(s):  
Thiago de Santana Santos ◽  
Erick Ricardo Silva ◽  
Ana Célia Faria ◽  
Francisco Veríssimo de Mello Filho ◽  
Samuel Porfírio Xavier

Supernumerary teeth (ST) are uncommon alterations of development that may appear in either of the dental arches and that are frequently associated with syndromes such as cleidocranial dysplasia and Gardner syndrome. Multiple ST in individuals with no other disease or syndrome are very rare. In view of this situation, correct diagnosis, treatment and evaluation of ST with the use of appropriate imaging techniques are highly important. This case report presents radiographic images of a nonsyndromic 12-year-old female patient who presented with 14 supernumerary teeth and was treated under general anesthesia, with the extraction of all ST in a single surgical intervention. During the postoperative period, the patient did not complain of pain nor did she present any signs or symptoms of infection. During late follow-up period, due to difficulty in traction of the maxillary right canine and mandibular left first premolar towards the dental arch, it was necessary to extract these teeth under local anesthesia. Radiographic examination 3 years after surgery revealed the absence of ST and of diseases related to the existence of these teeth.


2014 ◽  
Vol 75 (S 02) ◽  
Author(s):  
S. Heredero ◽  
J. Solivera ◽  
A. Romance ◽  
A. Dean ◽  
J. Lozano

2019 ◽  
Vol 98 (4) ◽  
pp. 178-180

Cavernous hemangiomas are benign tumours of mesodermal origin. Even though various localizations of hemangioma have been described in the literature, its occurrence in the greater omentum is very rare. Only symptomatic hemangiomas are indicated for surgical treatment. There are case reports presenting resection or surgical removal of the greater omentum with hemangioma because of mechanical syndrome, consumption coagulopathy, bleeding, infection or suspicion of a malignancy. This article presents a case report of a patient operated on for a suspicion of carcinomatosis of the greater omentum. Histological examination found hemangiomatosis in the resected greater omentum.


2017 ◽  
Vol 21 (1) ◽  
pp. 122-125 ◽  
Author(s):  
Abdoul A. Diouf ◽  
Moussa Diallo ◽  
Aissatou Mbodj ◽  
Omar Gassama ◽  
Mamour Guèye ◽  
...  

Author(s):  
Deepak Kaul ◽  
Farahnaz Muddebihal ◽  
Mohammed Anwar Ul Haque Chand

Osteomyelitis of maxillofacial skeleton is common in developing countries such as India. This case report describes successful surgical treatment of chronic suppurative osteomyelitis {CSO} of the mandible of a 35yr old female. The precipitating factor was thought to be eventful extraction in the {left } posterior body at the inferior border of mandible. Methods: Presurgical course of antibiotics ( Amoxycillin and metronidazole for 7 days and later followed by doxycycline for 1 month).Surgical debridement of the affected bone and reinforcing it with reconstruction plate using AO principles was done . Patient was kept on a high nutrient diet consisting of proteins. Conclusion: The case report demonstrates the typical features of CSO . The combination of the antibiotics therapy and surgical debridement was successful in the treatment of chronic suppurative osteomylitis.


RSBO ◽  
2016 ◽  
Vol 13 (1) ◽  
pp. 50
Author(s):  
Guilherme Dos Santos Trento ◽  
Paola Cotait de Lucas Cors ◽  
Naylin Danyelle de Oliveira ◽  
Leandro Eduardo Klüppel ◽  
Delson João da Costa ◽  
...  

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