A Rare Case of Mediastinal Emphysema Occurring during Dental Treatment

2017 ◽  
Vol 68 (6) ◽  
pp. 388-395
Author(s):  
Haruka Ihara ◽  
Makoto Miyamoto ◽  
Hirofumi Kumazawa ◽  
Hiroshi Iwai
2003 ◽  
Vol 65 (6) ◽  
pp. 563-566
Author(s):  
Takeshi ISHIGAMI ◽  
Yoshio URANO ◽  
Koji YAMANOUCHI ◽  
Toshikazu TAMURA

2021 ◽  
pp. 53-55
Author(s):  
L. A. Mamedova ◽  
O. I. Efimovich ◽  
I. V. Podojnikov ◽  
A. A. Podoinikova ◽  
A. A. Bashtovoy

Dens evaginatus (DE) is an odontogenic developmental abnormality that can be defined as a tubercle or bulge on the surface of a tooth, consisting of the outer layer of enamel, dentin, and possibly pulp. Early diagnosis and treatment of dental evagination is important to prevent untimely endodontic treatment, occlusal trauma, aesthetics, and the development of fissure caries. This pathology of tooth development is usually found on the premolars of the lower jaw as an additional tubercle or bulge between the buccal and lingual tubercles. DE in the maxillary premolar has been reported rarely in the literature. We report one such rare case in the maxillary premolar.Material and methods. The article describes a clinical case of treating a patient with dental evagination. For observation, we used X-ray images made with CBCT, as well as a photo protocol of the stages of patient treatment.Conclusions. Since this pathology is rare, the description of this clinical case will help doctors better understand the approaches to dental treatment with such anomalies in the development of tooth tissues. 


2018 ◽  
Vol 32 (2) ◽  
pp. 160-165
Author(s):  
Akitomo Kikuchi ◽  
Hiroyuki Adachi ◽  
Munetaka Masuda

2018 ◽  
Vol 149 (9) ◽  
pp. 794-800
Author(s):  
Daniela Carmagnola ◽  
Alberto Pispero ◽  
Elena Canciani ◽  
Claudia Dellavia ◽  
Christian Barbieri ◽  
...  

2017 ◽  
Vol 7 (1) ◽  
pp. 13
Author(s):  
Lisa Elizabeth Jacob ◽  
Anuna Laila Mathew ◽  
Omal Pattali Mohanan ◽  
Thomas Abraham ◽  
Jerin Thomas ◽  
...  

Aim: Sturge–Weber Syndrome, also known as encephalotrigeminal angiomatosis, is an uncommon, nonhereditary developmental anomaly. Methodology: A 48-year-old woman presented for routine dental treatment. She had a history of seizures and had a port wine stain on the right side of her face, which followed the distribution of the trigeminal nerve. Skull radiographs revealed “tram-track” calcifications. Conclusions: The early diagnosis of Sturge–Weber Syndrome requires a multidisciplinary approach. Oral health care professionals need adequate knowledge and understanding of the disease process to help diagnose and treat these patients.  How to cite this article: Jacob LE, Mathew AL, Omal PM, Abraham T, Thomas J, Varghese S. A Rare Case of Encephalotrigeminal Angiomatosis – A Case Report Int Dent Res 2017;7:13-6. Linguistic Revision: The English in this manuscript has been checked by at least two professional editors, both native speakers of English.


Author(s):  
S. K. Peng ◽  
M.A. Egy ◽  
J. K. Singh ◽  
M.B. Bishop

Electron microscopy and energy dispersive x-ray microanalysis (EDXA) are found to be very useful tools for identification of etiologic agents in pneumoconiosis or interstitial pulmonary disorders. Pulmonary interstitial fibrosis and granulomatosis are frequently associated with occupational and environmental pollution. Numerous reports of pneumoconiosis in various occupations such as coal and gold miners are presented in the literature. However, there is no known documented case of pulmonary changes in workers in the sandpaper industry. This study reports a rare case of pulmonary granulomatosis containing deposits from abrasives of sandpaper diagnosed by using EDXA.


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