Cemento-ossifying fibroma: A diagnostic dilemma

2021 ◽  
Vol 9 (1) ◽  
pp. 46
Author(s):  
Roopan Prakash ◽  
SMohamed Shahid ◽  
Hima Raj ◽  
KS Anil
2019 ◽  
Vol 08 (02) ◽  
pp. 136-138
Author(s):  
Musali Siddartha Reddy ◽  
Gollapudi Prakash Rao ◽  
Mohammed Imran ◽  
Uday Goutam Nookathota

AbstractA rare case of monostotic ossifying fibroma of the dorsal spine in a postpartum woman is being described. Ossifying fibromas of the spine are very rare tumors. They are components of benign fibro-osseous lesions. We report a case of an 18-year-old woman, who presented with complaints of weakness of both the lower limbs in the immediate postpartum period and was diagnosed with ossifying fibroma of the dorsal [D3] vertebral body. The tumor was excised followed by spinal stabilization. Histopathologic findings were consistent with ossifying fibroma. Postoperative period was uneventful. Monostotic variant of ossifying fibroma in the dorsal spine is an extremely rare tumor, and its presence in the postpartum period adds on to the diagnostic dilemma. Hence this case report can be kept in mind while evaluating a case presenting with complaints of weakness of both the lower limbs in the immediate postpartum period.


Author(s):  
Somayeh Nemati ◽  
Zahra Dalili ◽  
Fatemeh Shahsavari ◽  
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2014 ◽  
Vol 25 (5) ◽  
pp. 451-456 ◽  
Author(s):  
Maria Luiza Anjos Pontual ◽  
Andréa Anjos Pontual ◽  
Rafael Grotta Grempel ◽  
Leonardo Rocha Mendes Campos ◽  
Antonio de Lisboa Lopes Costa ◽  
...  

Osteoblastoma is a benign neoplasia and is uncommon in the jaws. In some cases, this lesion presents extremely aggressive local characteristics and is termed aggressive osteoblastoma. Because the clinical, radiographic and histopathologic characteristics are similar to those of a variety of benign and malignant tumors, it poses a diagnostic dilemma. This report presents a case of an aggressive osteoblastoma in the mandible and discusses the differential diagnosis of this lesion. A 13-year-old white male sought the Stomatology Clinic at the State University of Paraíba, Campina Grande, PB, Brazil, complaining of asymptomatic swelling on the left side of his face. Cone-beam computerized tomography showed a multilocular, hypodense bone lesion, located in the body of the left mandible and lower third of the ascending ramus. The initial diagnostic hypothesis was juvenile ossifying fibroma or osteosarcoma. After histopathologic examination, the final diagnosis was aggressive osteoblastoma. Surgical resection with a safety margin was performed. There was no evidence of recurrence after a follow-up period of 4 years.


2012 ◽  
Vol 4 (3) ◽  
pp. 156-159 ◽  
Author(s):  
Sarita Mishra ◽  
Sampan Singh Bist ◽  
Vinish Aggarwal

ABSTRACT Fibro-osseous lesions of the face and paranasal sinuses are relatively uncommon. The biological characteristics of fibroosseous lesions range from indolent to aggressive and from inflammatory to neoplastic. Cemento-ossifying fibroma is a rare, benign fibro-osseous lesion composed of lamellar bone, fibrous tissue and cementum. It is usually found in the jaw bone and presents in several variant pathological subtypes. The overlapping clinical, radiologic and histomorphologic features of these subtypes have led to diagnostic dilemma for the clinician, radiologist and the histopathologist. Clinically, the lesions are usually asymptomatic, slow-growing and wellcircumscribed. However, in very few cases, these tumors have demonstrated an aggressive course of development. Lesions that involve the midface and paranasal sinuses and presenting in earlier age tend to demonstrate aggressive behavior and rapid growth. We describe a case of a 13 years old young boy with aggressively behaving cemento-ossifying fibroma of the maxilla presenting acutely as right cheek swelling with gingival growth. How to cite this article Bist SS, Varshney S, Bhagat S, Mishra S, Aggarwal V. Juvenile Aggressive Cemento-ossifying Fibroma of the Maxilla. Int J Otorhinolaryngol Clin 2012;4(3):156-159.


Author(s):  
Sajedh M. Alturaiki ◽  
Ali Almomen ◽  
Ghaleb Al Azzeh ◽  
Abdulrahman Al Khatib ◽  
Nada Alshaikh

<p class="abstract"><strong>Background:</strong> Osteomas, ossifying fibromas, and fibrous dysplasia comprise a set of benign neoplasms known as fibro-osseous lesions (FO), which can arise in the paranasal sinuses. The vast majority of benign FO lesions (BFOL) are incidental findings on radiographs. They tend to be slow-growing tumors, and are infrequently symptomatic. The management strategy can vary significantly for theses lesions. This can range from serial, observations to aggressive surgical resection, based on symptomatology, size, and location of the lesion.</p><p class="abstract"><strong>Methods:</strong> Retrospective analysis of all the data of different symptomatic FO of the paranasal sinuses and the skull base was performed at King Fahad specialist hospital, Dammam, KSA (2006 to 2017).  </p><p class="abstract"><strong>Results:</strong> A total of 21 patients were identified; 10 (46.7%) patients were diagnosed with osteoma, 8 (38.1%) with fibrous dysplasia, 2 (9.5%) with ossifying fibroma and one (4.8%) with juvenile active ossifying (JAOF), 17 were adults and 4 were children, the range of f/u (3-60) months. 19 patients were managed by the endonasal endoscopic approach. They continue to be followed with no evidence of recurrence. Two cases required the revision combined endoscopic open approach to ensure adequate removal of the disease (residual and recurrence).</p><p><strong>Conclusions:</strong> Diagnostic dilemma of BFOL can be overcome with a combination of clinical, radiological and pathological criteria. Correct diagnosis of fibro-osseous tumors is crucial for adequate therapy as their treatment, prognosis, clinical aggressiveness and long term complications of individual entities vary significantly. Endoscopic computer-assisted surgery is the treatment of choice. Endoscopic resection remains a technical challenge. </p>


2021 ◽  
Vol 14 (3) ◽  
pp. e240952
Author(s):  
Santhosh Rao ◽  
Vandita Singh ◽  
Abdul Hafeez A ◽  
Subham S Agarwal

Psammomatoid Juvenile ossifying fibroma (PsJOF) is a rare benign fibro-osseous lesion characterised to grow to unusually large size very rapidly. Its usual presentation is in younger age group mostly children and predominately involving the Sino-Naso-Orbital region. Its aggressive nature gimmicks a malignant lesion but it is rather a benign lesion with a higher recurrence rate than the conventional ossifying fibroma but lacking metastatic potential. The high recurrence rate makes it essential that the lesion is not reconstructed immediately and thorough monitoring in the follow-up period. Lesion of such clinical importance needs to be diagnosed preoperatively to provide a better and radical surgical treatment option, but the variability in its presentation as seen in this case makes it even harder to diagnose. We aim to draw attention to the rare phenomena that PsJOF presents to help readers broaden their purview in diagnosis and thereby manage them accordingly.


2021 ◽  
Vol 18 (1) ◽  
pp. 102
Author(s):  
Fatemeh Mashhadiabbas ◽  
HassanMir Mohammad Sadeghi ◽  
ZahraSadat Torabi ◽  
Hamidreza Moslemi ◽  
Shervin Shafiei ◽  
...  

2010 ◽  
Vol 3 (2) ◽  
pp. 101-102
Author(s):  
Sudhir Naik

ABSTRACT Background Ossifying fibroma is an uncommon tumor of the craniofacial skeleton presenting in several variant histopathological subtypes. Ossifying fibroma is a benign fibro-osseous lesion that commonly involves the maxilla.1 Ossifying fibromas occur predominantly in women, frequently during the 3rd and 4th decades of life.1 The overlapping clinical and histopathological features of these subtypes have led to diagnostic dilemma and confusion.1 Complete excision of this tumor has become a necessity since it is notorious for recurrence.1 Aims To study and compare the clinical profiles of various types of ossifying fibroma and also the surgical approaches to the tumor. To discuss the diagnostic difficulties and controversies associated with the tumor. Setting Medical college referral hospital. Design Case reports of 4 patients presenting to our medical college OPD. Methods Planned surgical excision based on criteria. Results Four cases of different types of ossifying fibroma were successfully treated by various surgical approaches. 42 papers related to diagnostic and treatment aspects of ossifying fibroma were studied. Conclusion The diagnostic dilemma of ossifying fibroma can be overcome with a combination of clinical, radiological and pathological criteria. Complete surgical excision of the tumor is possible when surgery is based on preplanned criteria. Combination of 2 or more surgical approaches may be necessary in many cases in order to ensure complete clearance and prevent recurrence of the tumor.


2003 ◽  
Vol 50 (4) ◽  
pp. 171-178
Author(s):  
Arsa Minic

Fibro-osseous lesions of the jaws usually present a diagnostic dilemma for the clinician as well as the pathologist. This group includes fibrous dysplasia, ossifying fibroma, focal cemento-osseous dysplasia, periapical cemento-osseous dysplasia, and florid cemento-osseous dysplasia. As in other sites, appropriate clinicopathologic correlations are needed to reach a definitive diagnosis. The clinical and pathologic features of fibro-osseous lesions of the jaws are considered, including adequate therapeutic strategies.


2019 ◽  
Vol 25 ◽  
pp. 143-144
Author(s):  
Muhammad Ansar ◽  
Joseph Dillon
Keyword(s):  

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