scholarly journals Cherubism: Case Report and Review of Literature

2021 ◽  
Vol 21 (1) ◽  
pp. 44-54
Author(s):  
Sabah Nuri Mizel ◽  
◽  
Ali F Al-Zubaidee

Cherubism is an autosomal dominant, very rare benign fibro-osseous lesion, with an estimation of only 300 cases have been reported worldwide. Cherubism is characterized clinically by bilateral symmetrical self-limiting jaw enlargement starts in the childhood or early teens.Mandible is mostly affected although maxilla and zygomatic bones may be involved but to a lower extent), and is associated with tooth displacement and severe malocclusion. Histopathologically, it is indistinguishable from giant cell lesions therefore the clinical manifestations of the disease remain the Gold Stone. Keywords: Cherubism, mandible, maxilla, bilateral palatal swelling

2012 ◽  
Vol 2012 (jul12 2) ◽  
pp. bcr0120125703-bcr0120125703 ◽  
Author(s):  
V. Goni ◽  
N. R. Gopinathan ◽  
B. D. Radotra ◽  
V. K. Viswanathan ◽  
R. K. Logithasan ◽  
...  

Cureus ◽  
2016 ◽  
Author(s):  
Rishit Soni ◽  
Chirag Kapoor ◽  
Malkesh Shah ◽  
Amit Patel ◽  
Paresh Golwala

2020 ◽  
pp. 1-4
Author(s):  
Lyssa Van De Ginste ◽  
Amélie Dendooven ◽  
Jo Van Dorpe ◽  
Joris R. Delanghe ◽  
Jill Vanmassenhove ◽  
...  

2019 ◽  
Vol 56 (10) ◽  
pp. 1393-1403
Author(s):  
Tania Jhamb ◽  
Hayat Masood ◽  
Jeffrey Arigo ◽  
P. Emile Rossouw

Kniest dysplasia is a rare autosomal dominant chondrodysplasia that is characterized by distinct musculoskeletal and craniofacial irregularities. These craniofacial abnormalities include cleft palate, midface anomalies, tracheomalacia, and hearing loss. This article illustrates a case of Kniest dysplasia that presented for orthodontic treatment. The purpose of this literature review is to describe clinical manifestations, radiographic features, histopathological features, genetic mutation, and management of Kniest dysplasia.


2016 ◽  
Vol 33 (4) ◽  
pp. 218-221
Author(s):  
Moni Mohan Saha ◽  
Sukumar Saha ◽  
Ratan Lal Datta Banik ◽  
Md Mokter Hossain

A 25 years old male attended the skin & VD outpatient department of Khulna Medical College Hospital on 16th June, 2013 with complaints of multiple asymptomatic small rounded firm, cystic nodules that are adherent to the overlying skin of scortum. The microscopic examination of the cystic nodules showed the features of steatocystoma multiplex. This disorder, although it is asymptomatic, is a cosmetic threat to the patient. Only a few cases of the patients with an autosomal dominant mutation, who had keratin 17; have been reported. We are reporting here a case of steatocystoma multiplex of scortum in a 25 years old male along with review of literature.J Bangladesh Coll Phys Surg 2015; 33(4): 218-221


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