scholarly journals SIMPLE BONE CYST OF THE MANDIBLE: A CASE REPORT AND LITERATURE REVIEW

2021 ◽  
Vol 9 (10) ◽  
pp. 830-833
Author(s):  
Varun Muthuraman

Simple bone cyst is a benign pseudo cystic cavity in the bone that is less commonly associated in the maxillofacial region. The other synonyms are traumatic bone cyst or idiopathic bone cyst. These cysts are devoid of an epithelial lining and usually contain straw-colored fluid or is empty. Simple bone cyst is mainly seen in young individuals, frequently during the first and second decade of life. Here we report a case of simple bone cyst of a mandibular anterior region in a 21-year-old patient.

2012 ◽  
Vol 2 (3) ◽  
pp. 59 ◽  
Author(s):  
Charan Babu HS ◽  
Bhagawan Das Rai ◽  
Manju A. Nair ◽  
Madhusudan S. Astekar

Simple bone cysts (SBC) are pseudocysts occurring less commonly in the maxillofacial region. The uncertain and unclear etiopathogenesis led to numerous synonyms to refer this particular cyst. These cysts are devoid of an epithelial lining and are usually empty or contain blood or straw-colored fluid. In jaws initially it mimics a periapical cyst and later can lead to cortical bone expansion warranting for radical approach, which is seldom required. SBC is predominantly diagnosed in first two decades of life. Here we report a case of solitary bone cyst mimicking a periapical cyst of a mandibular molar in a 37-year-old patient.


Simple bone cyst (SBC) is an intraosseous pseudocyst without epithelial lining. The purpose of our report is to demonstrate case of a multilocular type of mandibular simple bone cyst. The precise consecutive cone beam computed tomography (CBCT) scans and a CT result of biopsy are presented. Revision of wide range of synonyms and a treatment options for multilocular (synonym: multicameral) type of SBCs are presented.


2020 ◽  
Vol 37 (1) ◽  
pp. e23-e25
Author(s):  
Lim Yi Wen ◽  
Sujaya Singh ◽  
Nor Fadhilah Binti Mohamad ◽  
Yen-Fa Toh ◽  
Alizan Abdul Khalil Khalil

2021 ◽  
pp. 106689692110082
Author(s):  
Sarah Al-Rawaf ◽  
Salem Alowami ◽  
Robert Riddell ◽  
Asghar Naqvi

Russell bodies are accumulation of immunoglobulin in plasma cells forming intracytoplasmic inclusions. Russell body colitis is rare with only 3 cases described in the English literature up to date. We report a 78-year-old male with cirrhosis showing prominent cecal infiltration of Russell body containing plasma cells. Plasma cells showed no nuclear atypia or mitoses, and no evidence of light chain restriction. In this article, we report a fourth case of Russell body colitis, that is unique in being localized to the cecum in contrast to the other 3, 1 of which was in an inflammatory polyp in the sigmoid colon, 1 in a rectal tubulovillous adenoma and 1 as part of diffuse gastrointestinal disease. This is therefore the first report of localized Russell body typhlitis, occurring in a cirrhotic patient in whom an adjacent erosion was likely nonsteroidal anti-inflammatory drug-associated, a combination that may have facilitated the formation of Russell bodies.


2012 ◽  
Vol 6 (1) ◽  
pp. 208-211 ◽  
Author(s):  
Nada O Binmadi ◽  
Risa Chaisuparat ◽  
Bernard A Levy ◽  
Nikolaos G Nikitakis

Sialolipoma is a relatively rare and fairly recently described as a variant of lipoma with salivary elements. Any site within the oral and maxillofacial region may be involved with the parotid gland being the most common location. Herein, we present a case of silaolipoma in lower lip. The clinical and histological features and differential diagnosis are discussed.


2019 ◽  
Vol 130 ◽  
pp. 267-270
Author(s):  
Yoshifumi Tao ◽  
Kenji Yagi ◽  
Hirotake Nishimura ◽  
Keijirou Hara ◽  
Shunji Matsubara ◽  
...  

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