scholarly journals SOLITARY PERIPHERAL OSTEOMA OF THE MANDIBLE: A CASE REPORT

2021 ◽  
Vol 9 (04) ◽  
pp. 194-196
Author(s):  
Sumalatha M.N ◽  
◽  
Gadiputi Sreedhar ◽  
Phani Himajadevi Vaaka ◽  
Kartheek Gandikota ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Maxillary Sinus ◽  
Rare Case ◽  
Facial Bones ◽  
Peripheral Osteoma ◽  
Pathologic Findings ◽  
Slow Growing

Osteomas are benign, slow growing oestrogenic tumours. They are often occurring in the craniofacial bones but rarely originate from the mandible. Osteomas have three varieties as central, peripheral and extra skeletal. Central and peripheral osteomas are often seen in the facial bones. Peripheral osteoma often located in the frontal, ethmoid and maxillary sinus, but rarely occurs in the jaws. Usually they are asymptomatic and discovered incidentally during radiological and clinical examinations. Osteomas are characterized with well-defined, rounded or oval radiopaque mass in the computed tomography. Herein, we report a rare case of peripheral osteoma of the lower part of the mandible in a 21-year-old male with radiologic and pathologic findings.

scholarly journals Large Peripheral Osteoma of the Mandible: A Case Report

2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Emel Bulut ◽  
Aydan Acikgoz ◽  
Bora Ozan ◽  
Omer Gunhan
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Cancellous Bone ◽  
The Body ◽  
Radiographic Examination ◽  
Facial Deformity ◽  
Peripheral Osteoma ◽  
Left Posterior ◽  
Peripheral Type ◽  
Slow Growing

Osteomas are benign, slow-growing osteogenic tumors commonly occurring in the craniofacial bones. Osteomas are characterized by the proliferation of compact and/or cancellous bone. It can be of a central, peripheral, or extraskeletal type. The peripheral type arises from the periosteum and is rarely seen in the mandible. The lingual surface and lower border of the body are the most common locations of these lesions. They are usually asymptomatic and can be discovered in routine clinical and radiographic examination. In this paper, we presented a large solitary peripheral osteoma located in the buccal surface of the left posterior mandible and causing facial deformity in a 37-year-old woman. Radiographic examination by computed tomography revealed radiopacity with a well-circumscribed, pedunculated mass approximately 3 cm in size. The osteoma was removed surgically, and no recurrence has been observed.

scholarly journals Solitary Peripheral Osteoma of the Angle of the Mandible

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Kapil Kshirsagar ◽  
Kalyani Bhate ◽  
Vivek Pawar ◽  
S. N. SanthoshKumar ◽  
Supriya Kheur ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Familial Adenomatous Polyposis ◽  
Cancellous Bone ◽  
Rare Case ◽  
Adenomatous Polyposis ◽  
Gardner’S Syndrome ◽  
Jaw Bones ◽  
Peripheral Osteoma ◽  
Histopathologic Findings ◽  
Slow Growing

Solitary peripheral osteoma is a benign, slow-growing osteogenic tumor arising from craniofacial bones such as the sinus, temporal, or jaw bones but rarely originating from the mandible. Osteoma consists of compact or cancellous bone that may be of peripheral, central, or extraskeletal type. Peripheral osteoma arises from the periosteum and is commonly a unilateral, pedunculated mushroom-like mass. Solitary peripheral osteomas are characterized by well-defined, rounded, or oval radiopaque mass in the computed tomography. Although multiple osteomas of the jaws are a hallmark of Gardner’s syndrome (familial adenomatous polyposis), nonsyndromic cases are typically solitary. Herein, we report a rare case of solitary peripheral osteoma of the angle of the mandible in a 27-year-old female with clinical, radiologic, and histopathologic findings.

scholarly journals Retroauricular Emphysema as a Late Complication After Bonebridge Implantation: Case Report

2021 ◽  
pp. 014556132110002
Author(s):  
Soňa Šikolová ◽  
Dagmar Hošnová ◽  
Klára Perceová ◽  
Michal Bartoš ◽  
Vít Kruntorád ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Postoperative Complications ◽  
Rare Case ◽  
Late Complication ◽  
Bone Conduction ◽  
Computed Tomography Scan ◽  
Artificial Opening ◽  
Low Incidence ◽  
Tomography Scan

Bonebridge (BB) is the first active implantation system for bone conduction that is placed fully under the skin. Experience suggests that BB is characterized by low incidence of postoperative complications. This case report presents a rare case of a 16-year-old girl with incidence of emphysema occurring over the implant 1 year after operation. We performed a computed tomography scan that showed pockets of gas above the floating mass transducer so we provided the revision surgery and sealed the artificial opening with fat from the earlobe and fibrin glue. Since that time, no air has collected in the retroauricular area and the implant has been fully functional.

scholarly journals A Diagnosis of Maxillary Sinus Fracture with Cone-Beam CT: Case Report and Literature Review

2014 ◽  
Vol 7 (2) ◽  
pp. 85-91 ◽  
Author(s):  
Selmi Yardimci Yilmaz ◽  
Melda Misirlioglu ◽  
Mehmet Zahit Adisen
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Maxillary Sinus ◽  
Cone Beam Ct ◽  
Maxillofacial Surgery ◽  
Maxillofacial Trauma ◽  
Cone Beam ◽  
Maxillofacial Region ◽  
Emergency Center ◽  
Frontal Wall

The purpose of this article is to present the case of maxillofacial trauma patient with maxillary sinus fracture diagnosed with cone-beam computed tomography (CBCT) and to explore the applications of this technique in evaluating the maxillofacial region. A 23-year-old male patient attempted to our clinic who had an injury at midface with complaints of swelling, numbness. The patient was examined before in emergency center but any diagnosis was made about the maxillofacial trauma. The patient re-examined clinically and radiographically. A fracture on the frontal wall of maxillary sinus is determined with the aid of CBCT. The patient consulted with the department of maxillofacial surgery and it is decided that any surgical treatment was not necessary. The emerging technique CBCT would not be the primary choice of imaging maxillofacial trauma. Nevertheless, when advantages considered this imaging procedure could be the modality of choice according to the case.

scholarly journals Peripheral osteoma of the mandibular crest: a short case study

2018 ◽  
Vol 24 (1) ◽  
pp. 29-32
Author(s):  
Arthur Fourcade ◽  
Benjamin Salmon ◽  
François Le Pelletier ◽  
Anne-Laure Ejeil
Keyword(s):  
Cortical Bone ◽  
Rare Case ◽  
Tooth Extraction ◽  
Histological Evaluation ◽  
Rare Form ◽  
Jaw Bones ◽  
Peripheral Osteoma ◽  
Slow Growing

Introduction: Osteoma is a benign slow-growing osteogenic neoplasm characterized by the proliferation of cancellous and/or cortical bone. Jaw bones are seldom affected. Observation: We observed a rare case of a patient with a peripheral mandibular osteoma, which was surgically removed. Comments: Frequently asymptomatic, a peripheral osteoma looks like a bony swelling that may be sessile or pedunculated. Imaging examinations show a well-circumscribed radio-opaque mass. Symptomatic osteomas must be surgically excised and submitted for histological evaluation. Conclusion: Excessive osseous healing following a tooth extraction may explain this rare form of osteoma.

Glandular odontogenic cyst associated with ameloblastoma occupying maxillary sinus: A rare case report

2016 ◽  
Vol 5 (3) ◽  
pp. 265
Author(s):  
Vagish KumarLaxman Shanbhag ◽  
Riaz Abdulla ◽  
Surendranathan Akhila ◽  
Maji Jose
Keyword(s):  
Case Report ◽  
Maxillary Sinus ◽  
Rare Case ◽  
Odontogenic Cyst ◽  
Glandular Odontogenic Cyst ◽  
Rare Case Report

scholarly journals A rare case of accessory maxilla: a case report and literature review of Tessier no. 7 clefts

2020 ◽  
Vol 48 (5) ◽  
pp. 030006052092568
Author(s):  
Ming Sun ◽  
Na Lv ◽  
Ya Xiao ◽  
Jiabin Li ◽  
Guangzhao Guan
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Rare Case ◽  
Clinical Presentation ◽  
Craniofacial Abnormalities ◽  
Supernumerary Teeth ◽  
Computed Tomography Images ◽  
Facial Clefts ◽  
Patient Prognosis ◽  
Patient’S History

Bilateral Tessier no. 7 clefts are rarely reported in the literature. Here, we describe the presence of accessory maxilla with supernumerary teeth in a patient who exhibited bilateral Tessier no. 7 clefts; the diagnosis was established based on the patient’s history, clinical presentation, and computed tomography images. A review of the available literature revealed 24 patients with Tessier no. 7 clefts from 2000 to 2020, including our patient. The most common clinical manifestation in patients with Tessier no. 7 clefts comprises bilateral facial clefts. Additionally, Tessier no. 7 clefts are more frequently found in boys or men, rather than in girls or women. The presence of an accessory maxilla with supernumerary teeth in a patient with bilateral Tessier no. 7 clefts is extremely rare. Early detection of craniofacial abnormalities is important, because it may influence patient prognosis and management.

scholarly journals A Case of Solid Pseudopapillary Neoplasm Spontaneously Ruptured Into the Duodenum: Case Report

2019 ◽  
Vol 103 (9-10) ◽  
pp. 461-467
Author(s):  
Seiji Natsume ◽  
Yoshiki Senda ◽  
Tsuyoshi Sano ◽  
Seiji Ito ◽  
Koji Komori ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Portal Vein ◽  
Rare Case ◽  
Pancreatic Head ◽  
Resected Specimen ◽  
Solid Pseudopapillary Neoplasm ◽  
Contrast Radiography ◽  
Pancreatic Head Tumor

There have been no reports of ruptured solid pseudopapillary neoplasm (SPN) into adjacent organs. A 22-year-old female was referred to our hospital for treatment of a pancreatic head tumor. Computed tomography (CT) examination at our hospital showed a 5-cm tumor containing air, although CT at a previous hospital revealed an 8-cm tumor without air. Thus, a spontaneous rupture of the tumor into the duodenum was suspected. Subtotal stomach preserving pancreaticoduodenectomy with combined resection of the portal vein was performed. Contrast radiography of resected specimen showed the medium injected into the tumor leaking out from the 2nd portion of the duodenum. Histologically, the patient was diagnosed as SPN. Microscopic invasion to the portal vein and duodenum were also confirmed. She did not experience any postoperative complications and has remained well without any signs of recurrence during 2 years of follow-up. Although there have been 14 studies reporting ruptured SPN, this is the first report of SPN that spontaneously ruptured into the duodenum. An extremely rare case of SPN of the pancreatic head that spontaneously ruptured into the duodenum was reported.

Sign in / Sign up

Export Citation Format

Share Document