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Odontogenic carcinosarcoma of the mandible: A case report.
Clin Case Rep
November 2024
Department of Oral and Maxillofacial Radiology, Faculty of Dentistry Tehran University of Medical Sciences Tehran Iran.
Key Clinical Message: Odontogenic carcinosarcoma, a rare and challenging diagnosis, was identified in a 60-year-old male through histopathology, revealing a biphasic neoplasm with malignant epithelial and mesenchymal components. Surgical resection is crucial for management, highlighting the importance of vigilant postoperative follow-up to ensure early detection of any recurrence.
Abstract: One rare mixed malignant odontogenic tumor is odontogenic carcinosarcoma, which comprises malignant epithelial and mesenchymal components.
Huge calcifying epithelial odontogenic tumor of the mandible and management with a teeth preserving surgical approach: a case report.
J Med Case Rep
November 2024
Department of Oral and Maxillofacial Surgery, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Background: Calcifying epithelial odontogenic tumor is a rare benign tumor that predominantly occurs in posterior sites of the mandible in adults.
Case Presentation: This case report describes a case of calcifying epithelial odontogenic tumor in a 37-year-old Iranian female with the chief complaint of swelling in the anterior region of the mandible and tooth displacement. This paper summarized the pathological findings, radiographical features and clinical management of the patient.
Histopathological spectrum of primordial odontogenic tumor with co-existing dentigerous cyst: 1 reported case of the world with a proposed 'updated diagnostic criteria'.
Diagn Pathol
October 2024
Private Practitioner, Smile-Align Dental Clinic, Bangalore, India.
Background: POT is a relatively newly described benign odontogenic tumor with very few cases registered to date. We present the 1st case of Primordial odontogenic tumor (POT) from Sub-Saharan Africa with unique clinicopathological features; also, this is the first case to report POT's existence as a Hybrid Odontogenic lesion (HOL), with a pertinent review of the literature.
Case Presentation: This was a 17-year-old patient who presented with slow-growing, painless posterior mandibular swelling.
Intraosseous myofibroma mimicking an odontogenic lesion: case report, literature review, and differential diagnosis.
World J Surg Oncol
September 2024
Oral and Craniomaxillofacial Surgery, University Hospital Basel, Spitalstrasse 21, Basel, 4031, Switzerland.
Article Synopsis
- Intraosseous myofibroma is a rare jaw tumor primarily affecting young boys, often not well understood in the medical community.
- A case study of a 2-year-old boy showed a painless swelling that was initially misdiagnosed, and further analysis revealed it was an intraosseous myofibroma after surgical removal.
- This case highlights the importance of thorough histopathological examination in diagnosing rare tumors in children and ensuring successful treatment outcomes.
Ewing's Sarcoma of Mandible: A Case Report with Review of Literature.
Int J Clin Pediatr Dent
February 2024
Faculty of Odontology, Department of Oral Surgery, Paris Cité, Hôpital Bretonneau AP-HP, Paris France.
Background: Ewing sarcoma (ES), a rare malignancy, comprises whatever the age, 4-15% of all primary bone tumors. It represents 1% of all malignant tumors in children and is the fourth most common bone malignancy after myeloma, osteosarcoma, and chondrosarcoma.
Case Description: A 12-year-old boy came to the Oral Surgery Department of Bretonneau Hospital referred by his dentist with a rapidly evolving swelling in the left mandibula for 6 weeks, which was initially diagnosed as a facial cellulitis.
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