Results 91 to 100 of about 11,182 (240)

PET-positive fibrous dysplasia - a potentially misleading incidental finding in a patient with intimal sarcoma of the pulmonary artery [PDF]

open access: yes, 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  

A rare case of McCune Albright syndrome [PDF]

open access: yes, 2019
McCune Albright syndrome is characterized by the clinical triad of precocious puberty, polyostotic fibrous dysplasia, and café-au-lait pigmentation. Authors reported the case of a 6 years old girl presenting with vaginal bleeding.
Banga, Siftie-Kaur, Patil, Pooja
core   +2 more sources

Facial palsy and Valsalva-induced vertigo in a patient with temporal bone cystic fibrous dysplasia

open access: yesInterdisciplinary Neurosurgery, 2022
A 29-year-old woman, known with polyostotic fibrous dysplasia, presented with facial palsy, vertigo, and ipsilateral neck pain. Radiology revealed a large temporal bone cyst, extruding intracranially, eroding the labyrinth and Fallopian canal ...
Glen J.F. Kemps   +4 more
doaj  

Craniofacial polyostotic fibrous dysplasia: A rare case

open access: yesDental Research Journal, 2014
Craniofacial fibrous dysplasia (FD) is one of three types of FD which can affect the craniofacial complex. It is the proliferation of cellular fibrous connective tissue intermixed with irregular bony trabecules. It is a developmental tumor-like condition
Fatemeh Owlia   +1 more
doaj   +1 more source

Monostotic Fibrous Dysplasia Involving the Mandible: A Case Report

open access: yesSAGE Open Medical Case Reports, 2020
Fibrous dysplasia (FD) is a skeletal developmental anomaly, which is non-hereditary and idiopathic in origin. It is characterized by the replacement of normal bone with the excess proliferation of fibrous tissue in irregular bony trabeculae.
Khalil Ibrahim Assiri
doaj   +1 more source

A rare case of polyostotic fibrous dysplasia detected on 18F-rhPSMA-7 PET/CT

open access: yesEuropean Journal of Nuclear Medicine and Molecular Imaging, 2020
The prostate-specific membrane antigen (PSMA) has been proven to show high expression in prostate cancer cells [1]. The high binding affinity and internalization of PSMA radioligands makes it an excellent molecular target for theranostics of prostate ...
Hong Wang, M. Eiber, T. Langbein
semanticscholar   +1 more source

Fibrous Dysplasia versus Juvenile Ossifying Fibroma: A Dilemma

open access: yesCase Reports in Dentistry, 2016
Fibrous dysplasia (FD) is a condition characterized by excessive proliferation of bone forming mesenchymal cells which can affect one bone (monostotic type) or multiple bones (polyostotic type). It is predominantly noticed in adolescents and young adults.
Sreelakshmi N. Nair   +7 more
doaj   +1 more source

Giant Polyostotic Fibrous Dysplasia: F-18-flourodeoxyglucose Positron Emission Tomography/Computerized Tomography and Radiologic Findings

open access: yesİstanbul Medical Journal, 2020
A 40-year-old man with polyostotic fibrous dysplasia underwent F-18-flourodeoxyglucose (FDG) positron emission tomography/computed tomography imaging to rule out a possible malignancy.
Melis Baykara Ulusan   +1 more
doaj   +1 more source

A Case of Atypical McCune-Albright Syndrome with Vaginal Bleeding [PDF]

open access: yes, 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

Incidence and Prevalence of Fibrous Dysplasia/McCune-Albright Syndrome: A Nationwide Registry-Based Study in Denmark

open access: yesJournal of Clinical Endocrinology and Metabolism
Context Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) is a rare genetic disorder. Incidence and prevalence are not well-studied. Epidemiological research is complicated by the rarity of FD/MAS, absence of registries, heterogeneous presentation, and
M. Meier   +6 more
semanticscholar   +1 more source

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