Results 1 to 10 of about 4,504 (202)

Polyostotic Fibrous Dysplasia With and Without McCune–Albright Syndrome—Clinical Features in a Nordic Pediatric Cohort [PDF]

Frontiers in Endocrinology, 2018
ObjectiveFibrous dysplasia (FD) presents as skeletal lesions in which normal bone is replaced by abnormal fibrous tissue due to mosaic GNAS mutation.
Pauliina Utriainen, Pauliina Utriainen, Pauliina Utriainen, Pauliina Utriainen, Helena Valta, Helena Valta, Sigridur Björnsdottir, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie, Eva Horemuzova, Eva Horemuzova   +13 more
doaj   +5 more sources

Polyostotic Fibrous Dysplasia of the Middle Finger [PDF]

Journal of the Belgian Society of Radiology
Teaching point: When a polyostotic lesion in the fingers is seen in a pediatric patient, fibrous dysplasia should be included in the differential diagnosis and a CT scan should be considered for the assessment of ground‑glass densities.
Tristán Igual-Pacheco, Nicolas De Vos, Jonas De Melio   +2 more
doaj   +2 more sources

Polyostotic fibrous dysplasia: Unveiling the complexity of a rare bone disorder through a case report [PDF]

Radiology Case Reports
Polyostotic fibrous dysplasia is a benign but potentially debilitating bone disorder characterized by the gradual replacement of normal bone with fibrous tissue.
Siham Nasri, Hicham Benramdane, Imane Kamaoui, Imane Skiker   +3 more
doaj   +2 more sources

Analysis of Series of Cases of Fibrous Dysplasia of Proximal Femur in Pediatric Population [PDF]

Journal of Orthopaedic Case Reports
Introduction: Fibrous dysplasia (FD) accounts for 5–7% of all benign bone tumors. It presents in two main forms – monostotic, which is more common affecting a single bone and presenting usually in 3rd decade of life; polyostotic, affecting several bones,
Sumit Gupta, Ankur Agarwal, Lokesh Raghav, Shray Jain, Amit Kumar Gupta   +4 more
doaj   +2 more sources

Polyostotic osteoid osteoma: A case report [PDF]

Radiology Case Reports, 2020
Osteoid osteomas are common, benign osteoblastic tumors that can occur in any bone in the body. They are almost always solitary, with only rare reports of multiple tumors in the same patient.
Kristopher de Ga, MD, Cyrus Bateni, MD, Morgan Darrow, MD, John McGahan, MD, R Lor Randall, MD, Dillon Chen, MD   +5 more
doaj   +3 more sources

Reactivating Sleeping Intramedullary Nail in a 16-Year-Old Female with Polyostotic Fibrous Dysplasia: A Case Report on Complications and Potential Solutions [PDF]

Life
Background: Fibrous dysplasia (FD) is a rare condition in which normal spongy and cortical bone is replaced by non-neoplastic fibrous tissue, leading to weakened bone matrix and increased risk of pathological fractures and deformities.
Marco Todisco, Marianna Viotto, Laura Campanacci, Giovanni Luigi Di Gennaro, Alessandro Depaoli, Gino Rocca, Giovanni Trisolino   +6 more
doaj   +2 more sources

Pediatric Fibrous Dysplasia of the Skull Base: Update on Management and Treatment [PDF]

Brain Sciences
Background: Fibrous dysplasia (FD) is often difficult for skull base surgeons to address. FD arises due to the abnormal proliferation of fibroblasts, ultimately resulting in immature osseous tissue replacing normal cancellous bone. When the skull base is
Pierce Spencer, Vidhatri Raturi, Amanda Watters, R. Shane Tubbs   +3 more
doaj   +2 more sources

Fibrous Dysplasia Polyostotic: When Radiology Clarifies the Diagnosis [PDF]

Global Pediatric Health
Fibrous 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, Sara Essetti PhD, Samia Obilat PhD, Fatima Chait PhD, Nourrelhouda Bahlouli PhD, Yousra Guelzim PhD, Siham El Haddad PhD, Nazik Allali PhD, Latifa Chat PhD   +8 more
doaj   +2 more sources

Superior survival in diffuse large B cell lymphoma of the bone with immune rich tumor microenvironment [PDF]

Blood Cancer Journal
With tumor genomic and gene-expression profiling (GEP), this study investigated the immune-molecular signatures of a unique cohort of diffuse large B-cell lymphoma of the bone (bone-DLBCL), including primary bone (PB-DLBCL, n = 52) and polyostotic-DLBCL (
Ruben A. L. de Groen, Fleur A. de Groot, Stefan Böhringer, Esther J. Kret, Lorraine M. de Haan, Troy Noordenbos, Susan Blommers, Romée E. W. Jansen, Tom van Wezel, Ronald van Eijk, Richard Raghoo, Dina Ruano, Liane te Boome, Valeska Terpstra, Henriette Levenga, Els Ahsmann, Eduardus F. M. Posthuma, Isabelle Focke-Snieders, Lizan Hardi, Wietske C. E. den Hartog, Anke van den Berg, Pim Mutsaers, King Lam, Marjolein W. M. van der Poel, Myrurgia Abdul Hamid, F. J. Sherida H. Woei-A-Jin, Ann Janssens, Thomas Tousseyn, Judith V. M. G. Bovée, Lianne Koens, Arjan Diepstra, Arjen H. G. Cleven, Marie José Kersten, Patty M. Jansen, Hendrik Veelken, Marcel Nijland, Tim J. A. Dekker, Joost S. P. Vermaat   +37 more
doaj   +2 more sources

Chondroblastic Osteosarcoma Associated with Previous Chronic Osteomyelitis Caused by Serratia liquefaciens in a German Shepherd Dog

Veterinary Sciences, 2022
Development of bone tumors as a result of chronic osteomyelitis represents a relatively rare and late complication in humans and animals. We described a malignant transformation (chondroblastic osteosarcoma) in a 7-year-old German shepherd with a history
Delia Franchini, Serena Paci, Stefano Ciccarelli, Carmela Valastro, Grazia Greco, Antonio Di Bello   +5 more
doaj   +1 more source