Benign fibro-osseous jaw lesions of periodontal membrane origin

Hammer, J; Scofield, Henry H.; Cornyn, John; Adamson, Jerome E.

doi:10.1097/00006534-196904000-00053

Cited by 19 publications

(10 citation statements)

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“…Several other jaw conditions [Hamner et al, 1968;Waldron et al, 1975;Melrose et al, 1976;Lyons, 1955;Jacobson and Hollender, 1980;Cannon et al, 1980;Sedano et al, 19821, unassociated with systemic abnormalities, are radiographically indistinguishable from the radiopaque lesions found in the form of 0 1 described here. The microscopic characteristics of the jaw lesions in some of these disorders are similar to those in our patients.…”

Section: Discussionmentioning

confidence: 56%

“…Because of the inadequate blood supply to the sclerotic masses, they may be prone to infection, either in extraction sites or through ulceration in the overlying mucosa. Once infected, large areas may sequestrate despite antibiotic therapy, a characteristic also found in patients with non-familial cemento-osseous dysplasia [Hamner et al, 1968;Waldron et al, 19751. Removing the sequestra will often result in uneventful healing. Thus, patients with the form of 01 described here should be followed closely in order to maintain the teeth in their best state of health.…”

Section: Discussionmentioning

confidence: 97%

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Osteogenesis imperfecta with unusual skeletal lesions: Report of three families

et al. 1985

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Thirteen individuals with osteogenesis imperfecta (OI) from three families were evaluated. All examined persons with OI had multilocular radiolucent, radiopaque, or radiolucent-radiopaque lesions of the maxilla and mandible. In most patients, the lesions involved the tooth bearing areas, but in two, the rami also were involved. Teeth were normal. Radiologic findings in the extragnathic skeleton included marked coarseness of trabeculae and diffuse osteopenia. It is proposed that these patients represent yet another dominantly inherited OI syndrome.

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Section: Discussionmentioning

confidence: 56%

Section: Discussionmentioning

confidence: 97%

Osteogenesis imperfecta with unusual skeletal lesions: Report of three families

et al. 1985

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“…This lesion was known by a variety of names like osteofibrous dysplasia, non osteogenic fibroma, cemento-ossifying fibroma, osteofibroma, fibro-osteoma, benign fibro osseous lesion of periodontal ligament origin. It was also known as osteofibrousdysplasia which was first described by Campanacci [12], where the lesion involved the tibia and fibula [13]. Jaffe and Lichtenstein described the above condition as nonosteogenic fibroma, popularly known as ''Jaffe-Campanacci syndrome'' [14].…”

Section: Discussionmentioning

confidence: 99%

“…Jaffe and Lichtenstein described the above condition as nonosteogenic fibroma, popularly known as ''Jaffe-Campanacci syndrome'' [14]. However, the term OF of jaw bones is being used since 1927 [13]. In 1968, OF's of jaw bones were first classified by 'Hemner' and cementum containing tumors were also grouped under them.…”

Section: Discussionmentioning

confidence: 99%

Retrospective Analysis of Ossifying Fibroma of Jaw Bones Over a Period of 10 Years with Literature Review

Mohanty

Gupta

Kumar

et al. 2013

J. Maxillofac. Oral Surg.

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Objective The purpose of this retrospective analysis is to document and discuss the features, treatment rendered and result of 25 histologically proven cases of ossifying fibromas of jaw bones operated by a single surgeon over a period of 10 years. Results Twenty-five patients were analyzed with a final diagnosis of ossifying fibroma comprising of 14 males (56 %) and 11 females (44 %). The age range was 11-45 years with a mean of 24.12 years. Mandible was involved in 72 % and maxilla in 28 % cases with a predominance of mandibular posterior [19 (76 %)] cases. The study showed similar findings in regard to clinical, radiographic & histological features of ossifying fibroma as compared to other studies. It also showed that the treatment rendered in the form of eneucleation, curettage or resection of the lesion depending on its stage and extent were adequate, as no recurrence has been reported till date. Conclusion Enucleation is preferred in small and well demarcated lesions. Curettage should be done in relatively large lesions with ill defined borders, not involving basal bone of mandible or cortical perforation. Resection should be reserved for aggressive and extensive cases with involvement of basal bone or perforation of cortices.

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“…OF have been more frequently observed in the third and fourth decades of life and has a higher incidence in the black population. [29][30][31] In our series, we had two cases aged 20 and 22 years.…”

Section: Ossifying Fibroma (Of)mentioning

confidence: 99%

Fibro-osseous lesions of the paranasal sinuses and the skull base

Alturaiki

Almomen

Azzeh

et al. 2018

Int J Otorhinolaryngol Head Neck Surg

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Background: 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.Methods: 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). Results: 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).Conclusions: 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.

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Benign fibro-osseous jaw lesions of periodontal membrane origin

Cited by 19 publications

References 0 publications

Osteogenesis imperfecta with unusual skeletal lesions: Report of three families

Osteogenesis imperfecta with unusual skeletal lesions: Report of three families

Retrospective Analysis of Ossifying Fibroma of Jaw Bones Over a Period of 10 Years with Literature Review

Fibro-osseous lesions of the paranasal sinuses and the skull base

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