Results 71 to 80 of about 1,845 (222)
Case Reports in Radiology, Volume 2025, Issue 1, 2025.Background Cherubism is a rare genetic disorder characterised by multilocular cystic lesions in the mandible and/or maxilla, which result in the typical cherub‐like face. Two forms of cherubism exist—hereditary (familial) and nonhereditary (nonfamilial)—and it usually occurs amongst children aged 2–7 years.
Seth Kwadjo Angmorterh +11 more
wiley +1 more source
Ivory Osteoma Of Temporal Bone [PDF]
, 2006 Osteomas are slow growing bony tumors common in fronto-ethmoid regions and rare in temporal bone. These are usually asymptomatic and require treatment mainly for cosmetic reasons.
Meher, Dr. Ravi
core +1 more source
Diagnóstico e tratamento da doença de Paget óssea [PDF]
, 2014 Objective:To conduct a literature review on the diagnosis and management of Paget’s disease of bone. Materials and methods:This scientific statement was generated by a request from the Brazilian Medical Association (AMB) to the Brazilian Society of ...
Bandeira, Francisco +8 more
core +3 more sources
PET-positive fibrous dysplasia - a potentially misleading incidental finding in a patient with intimal sarcoma of the pulmonary artery [PDF]
, 2018 Benign bone tumors can show an increased FDG uptake in FDG-PET/CT investigations. In the presented case, an incidentally detected PET-positive asymptomatic fibrous dysplasia was initially misinterpreted as a metastasis in a patient with intimal sarcoma ...
Bode, Beata +3 more
core
The surgical management of fibrous dysplasia of bone [PDF]
, 2012 The surgical management of Polyostotic Fibrous Dysplasia (FD) of bone is technically demanding. The most effective methods to manage the associated bone deformity remain unclear. The marked variation in the degree and pattern of bone involvement has made
Ippolito, Ernesto +5 more
core +4 more sources
Head &Neck, Volume 46, Issue 1, Page E1-E5, January 2024.Abstract Background McCune‐Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia (FD), café‐au‐lait skin pigmentation, and endocrine dysfunction. Extensive FD in the craniofacial region can present significant challenges in terms of disease control and carries a high risk of permanent visual impairment.
Moataz D. Abouammo +5 more
wiley +1 more source
Case Reports in Endocrinology, Volume 2024, Issue 1, 2024.We present a case of acromegaly associated with Arnold–Chiari 1 malformation and a literature review regarding this association, mainly focusing on the importance of a clear distinction between Chiari malformation and herniation of cerebellar tonsils (CTH).
Alessandro Ciarloni +2 more
wiley +1 more source
An unusual case of polyostotic fibrous dysplasia—A case report
Indian Journal of Dental Research, 2020 Fibrous dysplasia (FD) is a fibro-osseous lesion where normal bone and marrow is replaced with fibrous tissue, resulting in formation of bone that is weak and prone to expansion.
Kiran Suresh Jagtap +3 more
doaj +1 more source
A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding [PDF]
, 2011 Background: McCune-Albright syndrome (MAS) is a rare non-inherited disorder characterized by the clinical triad of precocious puberty, cafe-au-lait skin lesions, and fibrous dysplasia of bone.
Hashemipour, M. +4 more
core +1 more source