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Fibrous Dysplasia Polyostotic: When Radiology Clarifies the Diagnosis
Global Pediatric HealthFibrous dysplasia is a rare non-hereditary congenital condition characterized by 2 main forms: monostotic and polyostotic. Monostotic is the more common form, while polyostotic, often associated with a syndrome, is rarer. The case presented involves a 10-
Ihssane Lahlou PhD +8 more
doaj +1 more source
Differential diagnosis of fibrous dysplasia
Fogorvosi Szemle, 2018 Following taking the medical and dental history and performing a stomato-oncological screening of a 69-year-old female patient referred to our department, a panoramic X-ray acquisition was taken.
László Simonffy +3 more
doaj +1 more source
Vanishing (Disappearing) Bone Disease in children: a review [PDF]
, 2011 Vanishing bone disease is a very rare, peculiar destructive condition of the skeletal system resulting in spontaneous and progressive resorption and disappearance of osseous structures with replacement by vascular, fibrous connective tissue.
Nagaveni, N.B. +3 more
core +1 more source
3D‐Printed Talus‐Calcaneus Prosthesis in Treating Ewing's Sarcoma: A Case Report
Orthopaedic Surgery, Volume 17, Issue 1, Page 288-294, January 2025.The reconstruction of the ankle is significantly challenged by the bone defect following talus‐calcaneus tumor resection. In this study, personalized talus‐calcaneus prosthesis was printed by 3D printing technology to reconstruct ankle and restore joint function of patient.
Weiyi Wang +10 more
wiley +1 more source
Benign fibro-osseous lesions of the maxillas: analysis of 11 cases [PDF]
, 2014 Introduction: A study is made of the principal characteristics of the oral lesions biopsied in our Service of Oral Surgery and histologically diagnosed as corresponding to fibro-osseous lesions of the maxillas.
Berini Aytés, Leonardo +3 more
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Radiologic Aspects of Segmental Odontomaxillary Dysplasia: A Case Report
Case Reports in Dentistry, Volume 2025, Issue 1, 2025.Segmental odontomaxillary dysplasia (SOD) is a rare nonheritable unilateral developmental disorder characterized by dental, bone, and soft tissue abnormalities. A 13‐year‐old female patient presented with mild facial asymmetry. Clinical examination revealed right maxillary enlargement and gingival overgrowth.
Alessandra Landim +8 more
wiley +1 more source
Alendronato a dosis bajas en el tratamiento de la enfermedad de paget ósea [PDF]
, 2002 Objetivo: Reducir la dyspepsia, nausea o úlcera esofágica como reacciones adversas del alendronato como antipagético administrando la mitad de la dosis.
Argüelles Sanginés, Francisco +5 more
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Clinical, microscopic and imaging findings associated to Mccune-Albright syndrome: report of two cases [PDF]
, 2008 McCune-Albright syndrome is characterized by the triad café-au-lait cutaneous spots, polyostotic fibrous dysplasia and endocrinopathies. This article presents two cases of McCune-Albright syndrome in a middle-aged woman and a young girl.
BRENTEGANI, Luiz Guilherme +4 more
core +1 more source
Case Reports in Endocrinology, Volume 2025, Issue 1, 2025.Background: Fibrous dysplasia (FD) is a rare congenital bone disease. Denosumab, a monoclonal antibody targeting nuclear factor kappa‐B ligand (RANKL), suppresses osteoclast activity and exhibits therapeutic potential for FD. Case Presentation: We present the case of an adult female patient diagnosed with FD who had undergone 7 treatment cycles of ...
Danni Liu +5 more
wiley +1 more source
Benign fibro-osseous lesions of the maxillas : analysis of 11 cases [PDF]
, 2008 Introduction: A study is made of the principal characteristics of the oral lesions biopsied in our Service of Oral Surgery and histologically diagnosed as corresponding to fibro-osseous lesions of the maxillas.
Berini Aytés, Leonardo +3 more
core