scholarly journals Trabecular Juvenile Ossifying Fibroma Management by Virtual Surgical Planning, Piezoelectric Surgery, and Simultaneous Patient Specific Implant (PSI) Reconstruction

2020 ◽  
Vol 4 (2) ◽  
pp. 39-46
Author(s):  
Henry Aldana ◽  
Martin Orozco ◽  
Leonardo Ordoñez ◽  
Clara Estrada ◽  
Camilo Mosquera
Keyword(s):  
Surgical Planning ◽  
Patient Specific ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Craniofacial Skeleton ◽  
Complete Excision ◽  
Juvenile Ossifying Fibroma ◽  
Piezoelectric Surgery ◽  
Children And Young Adults ◽  
The Right

Trabecular juvenile ossifying fibroma is a rare fibro-osseous lesion affecting the craniofacial skeleton occurring commonly in children and young adults. Tumor clinical behavior is highly aggressive with invasion of adjacent anatomic structures. Because of its high recurrence rate complete excision is necessary, but this one could be facial mutilating. This case report presents a 23-year-old female patient with a trabecular juvenile ossifying fibroma of the right maxilla, expanding into the orbit and zygomatic bone. The report also shows the multidisciplinary surgical management of this lesion with successful preservation of optic nerve function and facial aesthetics.

scholarly journals Juvenile psammomatoid ossifying fibroma of maxilla: A case report

2022 ◽  
Vol 7 (4) ◽  
pp. 247-249
Author(s):  
Vasvani M Dimple ◽  
Irom Urmila ◽  
Tuladhar Alisha ◽  
Neeraj ◽  
Chug Ashi
Keyword(s):  
Recurrence Rate ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Complete Excision ◽  
Juvenile Ossifying Fibroma ◽  
Histological Variant ◽  
Oral Approach ◽  
Psammomatoid Ossifying Fibroma ◽  
Very High

Juvenile psammomatoid ossifying fibroma is histological variant of juvenile ossifying fibroma, a fibro-osseous tumor of craniofacial bones with benign but potentially aggressive nature. Complete excision of tumor is essential as it is associated with very high recurrence rate. We have reported here a case of juvenile ossifying fibroma- a psammomatoid variety present in right maxilla in a 13-year old male child. Complete excision of tumor was done through intra-oral approach with the 2.5 years of follow up shows no recurrence.Juvenile psammomatoid ossifying fibroma is fibro-osseous tumor of craniofacial bones with benign but potentially aggressive nature. Complete excision of tumor is essential as it is associated with very high recurrence rate.

scholarly journals Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report

2016 ◽  
Vol 6 (1) ◽  
pp. 45-51
Author(s):  
Deepa Das Achath ◽  
Abhishek Sanjay Ghule ◽  
Preeti Kanchan-Talreja ◽  
Sunanda Bhatnagar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histological Analysis ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Appropriate Treatment ◽  
Juvenile Ossifying Fibroma ◽  
Rare Case Report

ABSTRACT Fibroosseous lesions of the jaws, including juvenile ossifying fibroma (JOF), pose diagnostic and therapeutic difficulties due to their clinical, radiological, and histological variability. There are two histological varieties of it, one as psammomatoid type and second as trebacular type; here, we present a trebacular type, which is a rare variety. After the clinical examination, radiological and histological analysis, it was diagnosed as juvenile trebacular ossifying fibroma. Although JOF is an uncommon clinical entity, its aggressive local behavior and high recurrence rate means that it is important to make an early diagnosis, apply the appropriate treatment, and, especially, follow-up the patient over the long term. How to cite this article Ghule AS, Achath DD, Kanchan- Talreja P, Bhatnagar S. Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report. J Contemp Dent 2016;6(1):45-51.

Juvenile Ossifying Fibroma in a Juvenile Diabetic: A Case Report with Surgical Management

2010 ◽  
Vol 1 (1) ◽  
pp. 59-64
Author(s):  
Jagadish Hosmani ◽  
Sujata M Byahatti ◽  
Ranganath Nayak ◽  
Ramakant Nayak ◽  
Bhushan Jayade
Keyword(s):  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Histopathological Diagnosis ◽  
Massive Growth ◽  
Juvenile Ossifying Fibroma ◽  
Histological Variants ◽  
Long Term Follow Up ◽  
Juvenile Diabetic

ABSTRACT Juvenile ossifying fibroma (JOF) is a highly aggressive uncommon fibro-osseous lesion occurring in the facial bones. Two histological variants of JOF, i.e. trabecular and psammomatoid have been reported. Here we present a case of a 20-year-old juvenile diabetic patient with massive growth on her left side of the jaw which was diagnosed as juvenile ossifying fibroma. This huge aggressive mass in the left side of the mandible had lead to complete lingual tilting of molars and premolars. After clinical and radiological examination, a biopsy led to the histopathological diagnosis of mixed variant of juvenile ossifying fibroma. The required surgical treatment (hemimandibulectomy) was undertaken under GA. The aggressive local behavior and high recurrence rate of JOF emphasizes the need for an early diagnosis, and appropriate radical treatment with long-term follow-up. One such case is reviewed and discussed in detail in the following article.

scholarly journals Virtual Surgical Planning and Piezoelectric Surgery in Tumor Extirpative Surgery Aimed at Inferior Alveolar Nerve Preservation

2017 ◽  
Vol 2017 ◽  
pp. 1-6
Author(s):  
Eric L. Chung ◽  
Faizan Alawi ◽  
Anh D. Le ◽  
Rabie M. Shanti
Keyword(s):  
Computer Aided Design ◽  
Surgical Planning ◽  
Inferior Alveolar Nerve ◽  
Benign Tumors ◽  
Ossifying Fibroma ◽  
Nerve Preservation ◽  
Virtual Surgical Planning ◽  
Piezoelectric Surgery ◽  
Computer Aided ◽  
Cad Cam

A myriad of extirpative surgical protocols for the management of benign tumors of the jaws have been presented in the literature. Through significant advancements in computer-aided design and computer-aided manufacturing (CAD/CAM) technology and surgical instrumentation, today surgeons have at their disposal robust technology-driven techniques that are aimed at improving surgical outcomes. Our goal is to investigate the benefits of implementing virtual surgical planning (VSP) in conjunction with piezoelectric surgery (PES) to ensure success while minimizing the risk of complications during extirpation of tumors of the mandible. This case report describes the successful extirpation of an ossifying fibroma of the mandible in an adult patient using both VSP and PES.

scholarly journals Peripheral Ossifying Fibroma in Rare Site: A Clinicopathological Report

2015 ◽  
Vol 6 (2) ◽  
pp. 60-64
Author(s):  
Nagaraj Kalburgi ◽  
Apoorva Kamat ◽  
Jane Mary ◽  
Ankita Kotecha
Keyword(s):  
Female Patient ◽  
Benign Tumor ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Common Occurrence ◽  
Complete Excision ◽  
Peripheral Ossifying Fibroma ◽  
Rare Site ◽  
Interdental Papilla ◽  
Pedunculated Tumor

ABSTRACT Peripheral ossifying fibroma (POF) is a slowly growing benign tumor with a high recurrence rate. It is a common occurrence in the maxilla. A nodular mass, either pedunculated or sessile, usually emanating from the interdental papilla. Complete excision of the lesion, including the periosteum, is important to prevent recurrence. Peripheral ossifying fibroma occurring in the mandible at the age of 50 in the posterior mandible is an occasional entity. This article describes a case of a female patient with a slowly growing pedunculated tumor in the posterior mandible, which was diagnosed as POF. How to cite this article Koregol AC, Kalburgi N, Kamat A, Mary J, Kotecha A. Peripheral Ossifying Fibroma in Rare Site: A Clinicopathological Report. J Health Sci Res 2015;6(2):60-64.

Juvenile Ossifying Fibroma of a 15-Year-old Girl: A Case Report

2021 ◽  
Author(s):  
MA Awal
Keyword(s):  
Case Report ◽  
Recurrence Rate ◽  
Female Child ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Surgical Removal ◽  
Facial Deformity ◽  
Maxillofacial Region ◽  
Long Period ◽  
Juvenile Ossifying Fibroma

Juvenile ossifying fibroma is a locally aggressive, benign fibro-osseous tumor. It usually occurs in young children and arises in the maxillofacial region. It has a high recurrence rate. This pathology would be diagnosed and treated as early as possible because of its rapidly progressive and osteolytic nature which may complicate the surgical removal if left untreated over a long period. The present case is diagnosed as Juvenile ossifying fibroma involving the maxilla causing facial deformity, proptosis, and nasal obstruction in a 15-year-old female child.

scholarly journals Synchronous Juvenile ossifying Fibroma in maxilla and mandible- A case report

2014 ◽  
Vol 4 (2) ◽  
pp. 54-57
Author(s):  
B Shrestha ◽  
S Subedi ◽  
S Pandey
Keyword(s):  
Histopathological Examination ◽  
Ossifying Fibroma ◽  
Medical College ◽  
Appropriate Treatment ◽  
Juvenile Ossifying Fibroma ◽  
Long Term Follow Up ◽  
Maxilla And Mandible ◽  
The Right

Juvenile ossifying fibroma (JOF), one of the fibroosseous lesions is an uncommon clinical entity and involving both jaw is even rarer. Here, we present the case of a 15-year-old female patient with synchronous occurrence of JOF in the right sided maxilla and in the periapical area of mandibular right premolar molar region. After the clinical, radiographical and histopathological examination, the surgical treatment was carried out and the patient was kept under long term follow up. Owning to its aggressive local behaviour and high recurrence, early diagnosis, appropriate treatment and long term regular follow up are of prime importance. DOI: http://dx.doi.org/10.3126/jcmc.v4i2.10867 Journal of Chitwan Medical College 2014; 4(2): 54-57

scholarly journals Massive Juvenile Ossifying Fibroma of the Frontal Bone

2014 ◽  
Vol 7 (1) ◽  
pp. 36-39
Author(s):  
SS Bist ◽  
Sarita Mishra ◽  
Vinish Agrawal ◽  
Bhartandu Bharti ◽  
Himanshual Kala
Keyword(s):  
Lateral Displacement ◽  
Fibrous Tissue ◽  
Frontal Bone ◽  
Ossifying Fibroma ◽  
Lamellar Bone ◽  
Craniofacial Skeleton ◽  
Younger Patients ◽  
Osseous Lesion ◽  
Juvenile Ossifying Fibroma ◽  
Slow Growing

ABSTRACT Ossifying fibroma is a rare, benign fibro-osseous lesion composed of lamellar bone and fibrous tissue. It occurs as an osseous lesion in the craniofacial skeleton. Clinically, lesions are usually asymptomatic, slow-growing and well-circumscribed. However, in very few cases, particularly in younger patients these tumors have demonstrated an aggressive course of development. Surgical management via a wide local excision is a necessity since it is notorious for recurrence, especially paranasal sinuses lesions. Here, we describe a case of a 9-year- old male child who had left forehead swelling with painless, progressive proptosis and downward lateral displacement of the globe for approximately 8 months. Computed tomography showed a massive expansile lesion involving the left frontal bone. The mass was excised surgically via a Lynch Howarth approach and proved histopathologically to be a juvenile ossifying fibroma. The radiological interpretation will be discussed which is helpful for diagnosis and selecting appropriate surgical approach in growing child. How to cite this article Bist SS, Mishra S, Bharti B, Agrawal V, Kala H. Massive Juvenile Ossifying Fibroma of the Frontal Bone. Clin Rhinol An Int J 2014;7(1):36-39.

scholarly journals Juvenile psammomatoid ossifying fibroma with fluid–fluid levels: an unusual presentation

2021 ◽  
Vol 52 (1) ◽  
Author(s):  
Linda Kalliath ◽  
D. Karthikeyan ◽  
Nataraj Pillai ◽  
Deepthi Padmanabhan ◽  
Partheeban Balasundaram ◽  
...  
Keyword(s):  
Recurrence Rate ◽  
Nasal Obstruction ◽  
Histopathological Examination ◽  
Young Patients ◽  
High Recurrence Rate ◽  
Ossifying Fibroma ◽  
Imaging Findings ◽  
Juvenile Ossifying Fibroma ◽  
Adjacent Structures ◽  
Facial Swelling

Abstract Background Juvenile ossifying fibroma is an uncommon benign fibro-osseous tumor commonly involving the craniofacial skeleton of young patients with locally aggressive behavior and a high recurrence rate. Depending on the site of involvement it can present clinically as nasal obstruction, facial swelling, or proptosis. Case presentation Here we present a case of juvenile ossifying fibroma with an aneurysmal bone cyst component in the left nasal cavity in a 15-year-old boy who presented with gradually progressing left-sided nasal obstruction. Imaging findings were consistent with juvenile ossifying fibroma. Endoscopic resection of the tumor was done, and histopathological examination revealed it to be a psammomatoid variant of juvenile ossifying fibroma. Here we discuss its imaging findings, differential diagnosis, treatment options, and histopathological features. Conclusion Despite being a slow-growing benign tumor, early diagnosis and treatment are necessary due to its locally aggressive nature and invasion of adjacent structures. Complete surgical resection is the mainstay of treatment because of the high recurrence rate.

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