Results 31 to 40 of about 1,838 (183)

An unusual case of polyostotic fibrous dysplasia—A case report

open access: yesIndian 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

Delayed Diagnosis of McCune–Albright Syndrome

open access: yesCase Reports in Genetics, Volume 2021, Issue 1, 2021., 2021
Background. McCune–Albright syndrome (MAS) is a rare heterogeneous genetic disorder that is characterized by a triad of polyostotic fibrous dysplasia (FD), café au lait spots (CAL), and multiple hyperfunctional endocrinopathies. In general, it is diagnosed clinically.
Bereket Fantahun   +2 more
wiley   +1 more source

UniToPatho, a labeled histopathological dataset for colorectal polyps classification and adenoma dysplasia grading [PDF]

open access: yes, 2021
Histopathological characterization of colorectal polyps allows to tailor patients' management and follow up with the ultimate aim of avoiding or promptly detecting an invasive carcinoma. Colorectal polyps characterization relies on the histological analysis of tissue samples to determine the polyps malignancy and dysplasia grade.
arxiv   +1 more source

Polyostotic fibrous dysplasia (McCune-Albright) with rare multiple epiphyseal lesions in association with aneurysmal bone cyst and pathologic fracture

open access: yesRadiology Case Reports, 2021
Fibrous dysplasia, including McCune-Albright syndrome, is a genetic, non-inheritable benign bone disorder that may involve a single or multiple bone, typically occurring in the diaphysis or the metaphysis of long bones. In very rare instances polyostotic
Alvaro Burdiles, MD   +7 more
doaj  

Radioiodine treatment in McCune-Albright syndrome with hyperthyroidism

open access: yesIndian Journal of Endocrinology and Metabolism, 2012
McCune-Albright syndrome (MAS) is a sporadic disease characterized by polyostotic fibrous dysplasia, "café-au-lait" spots and hyperfunctional endocrinopathies.
Dhritiman Chakraborty   +5 more
doaj   +1 more source

Sarcomatous transformation (Leiomyosarcoma) in polyostotic fibrous dysplagia

open access: yesIndian Journal of Endocrinology and Metabolism, 2013
Malignant changes in polyostotic fibrous dysplasia are very rare. Most common malignancies reported are osteosarcoma and fibrosarcoma, chondrosarcoma and malignant fibrous histiocytoma. Here, we report a previously diagnosed case of fibrous dysplasia who
M K Garg   +5 more
doaj   +1 more source

Polyostotic fibrous dysplasia without craniofacial involvement: An unusual presentation

open access: yesJournal of the Scientific Society, 2018
Fibrous dysplasia (FD) is a benign bone disorder resulting into the replacement of bone with fibrous tissue. These fibrous bones are prone for deformities, pain, and pathological fractures, hence requiring treatment.
Seema Sharma   +3 more
doaj   +1 more source

Shepherd’s Crook Deformity with Pathological Femur Neck Fracture in a Patient with Fibrous Dysplasia Managed with Proximal Femoral Nailing and Valgus Osteotomy [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2021
Fibrous dysplasia is a rare condition in which bone is replaced by fibroosseous tissue. It is a benign condition, divided into monostotic and polyostotic fibrous dysplasia, which accounts for about 5-7% of all benign bone tumours. Here, authors reported
Neetin P Mahajan   +4 more
doaj   +1 more source

In-silico modeling of the micromechanics of fibrous scaffolds and stiffness sensing by cells [PDF]

open access: yes, 2021
Mechanical properties of the tissue engineering scaffolds are known to play a crucial role in tissue regeneration. Here, we have utilized discrete network and finite element models to study fibrous scaffold mechanics and its dependence on structure.
arxiv   +1 more source

Pagetoid polyostotic fibrous dysplasia [PDF]

open access: yesBMJ Case Reports, 2015
Fibrous dysplasia (FD) is a benign skeletal lesion occurring due to mutation of Gs α gene and involves one or multiple bones. We present a case of a 30-year-old female patient, with a 1-year history of swelling under her right eye that had gradually increased in size.
Neeta Mohanty   +3 more
openaire   +2 more sources

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