Results 51 to 60 of about 263,337 (158)

Bone Diseases of the Jaws

open access: yesInternational Journal of Dentistry, Volume 2010, Issue 1, 2010., 2010
Lesions specific for the jaws and not occurring in any other bones mostly are related to the teeth or to odontogenic tissues. Moreover, the jaws may harbor nonodontogenic bone lesions not seen in any other part of the skeleton. This paper pays attention to the diseases that are specific for the jaws, odontogenic as well as nonodontogenic.
Pieter Johannes Slootweg   +1 more
wiley   +1 more source

Diagnostic aspects of juvenile ossificant fibroma: A case study [PDF]

open access: yes, 2020
Juvenile ossifying fibroma is an uncommon, fast-growing benign neoplasm classified within the group of fibro-osseous lesions that directly affect the face and the jaws.
Ramos, Rogério Rodrigo   +19 more
core   +1 more source

Psammomatoid juvenile aggressive ossifying fibroma of mandible

open access: yesNational Journal of Maxillofacial Surgery, 2012
A female patient, aged 14 years, came to dental OPD, with a large swelling of the right mandibular region, progressing since 4-5 years. The swelling initially started with a small size and later it became a large swelling extending from left lower premolar region to right mandibular angle region.
Rao, Sudhapalli Chidanand   +5 more
openaire   +3 more sources

Extraosseous Cemento‐Ossifying Fibroma of the Cheek

open access: yesScholarly Research Exchange, Volume 2009, Issue 1, 2009., 2009
Background. Cemento‐ossifying fibroma (COF) is a relatively rare tumor of the maxillary bones, classified among the fibro‐osseous lesions Feller et al. (2004). The lesion that develops appears within the bone, although in some cases, it involves the soft tissues Kaufmann et al. (1999), Jung et al. (1999). In literature there is not report of COF in the
Gianluigi Longobardi   +4 more
wiley   +1 more source

Psammomatoid juvenile ossifying fibroma of maxilla in a 45-year-old female patient

open access: yesSRM Journal of Research in Dental Sciences, 2013
Juvenile ossifying fibroma (JOF) is an uncommon, benign, yet aggressive fibro-osseous lesion of the jaws commonly occurring in children and young adults and affects equally both males and females. Maxilla is affected more often than mandible.
Sanchita Kundu   +3 more
doaj   +1 more source

First presentation of a frameshift mutation in the SETD2 gene of a juvenile psammomatoid ossifying fibroma (JPOF) associated with an aneurysmal bone cyst

open access: yesDiagnostic Pathology, 2021
Background The rarity of juvenile psammomatoid ossifying fibroma (JPOF) and lack of cytogenetic studies prompted us to report a novel SETD2 gene mutation in a benign odontogenic tumour.
A. Toferer   +4 more
doaj   +1 more source

Case Report: rare hybrid lesion of a central giant cell granuloma within a juvenile ossifying fibroma [version 1; peer review: 1 approved, 2 approved with reservations]

open access: yesF1000Research, 2019
Central giant cell granuloma (CGCG) is classified by the World Health Organization as a benign bone lesion. It is found anteriorly in the mandible, with most of the cases crossing the midline.
Hadeer Rizk Saad   +2 more
doaj   +1 more source

Juvenile Psammomatoid Ossifying Fibroma (JPOF) of Proximal Radius: A Rare Entity

open access: yes, 2017
Background: Juvenile psammomatoid ossifying fibroma (JPOF) is a rare fibro-osseous lesion that usually occurs in the facial bones.
Iftikhar Ahmed Mukhtar   +2 more
core   +1 more source

Juvenile psammomatoid ossifying fibroma: a rare cause of unilateral proptosis [PDF]

open access: yesBMJ Case Reports, 2011
This is case of a young girl who presented with unilateral proptosis. Imaging (CT & MRI) revealed an expansile lytic bony tumour involving the left frontal bone and orbital roof. The globe was displaced but uninvolved. Complete surgical resection was done and histopathology revealed psammomatoid bodies diagnostic of juvenile psammomatoid ossifying ...
Rajesh, Tandon   +5 more
openaire   +2 more sources

Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2 ‐Related Disorders to a Syndromic Multiple Tumor Phenotype

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 7, July 2025.
ABSTRACT SETD2 has an essential role in epigenetic regulation. SETD2 pathogenic variants cause neurodevelopmental disorders (SETD2‐NDDs) that most commonly include various degrees of intellectual disability and behavioral disorders, macrocephaly, brain malformations, and generalized overgrowth.
Marie Lucain   +11 more
wiley   +1 more source

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