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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, Imane Kamaoui, Imane Skiker   +2 more
exaly   +4 more sources

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   +3 more sources

Polyostotic fibrous dysplasia

Journal of the Belgian Society of Radiology, 2013
Background: A 51-year-old male was referred to the hospital with pain on the right side of the thorax, without any apparent trauma. There was no medical history. He had a nonproductive cough and smoked 15 cigarettes a day.
BJ Schouten, HM Suliman
doaj   +5 more sources

Fibrous Dysplasia Polyostotic: When Radiology Clarifies the Diagnosis

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-
Latifa Chat, Nazik Allali, Siham El Haddad   +2 more
exaly   +2 more sources

Craniofacial polyostotic fibrous dysplasia

Contemporary Clinical Dentistry, 2010
An unusual case of fibrous dysplasia involving right craniofacial region in a female is reported. The clinical features, radiological findings, and treatment have been discussed.
Yadavalli Guruprasad, Chandan Prabhakar
doaj   +3 more sources

Management of polyostotic eosinophilic granuloma

Dental Research Journal, 2012
Eosinophilic granuloma is a rare disease which is difficult to diagnose clinically and radiographically. Localized Langerhans′ cell histiocytosis, previously known as eosinophilic granuloma, mainly affects the skull, mandible, vertebrae, pelvis and ribs ...
Ajay Parihar, Vilas Newaskar
doaj   +3 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

Craniomaxillofacial Fibrous Dysplasia Improved Cosmetic and Occlusal Problem by Comprehensive Treatment: A Case Report and Review of Current Treatments

Diagnostics, 2022
Fibrous dysplasia (FD) is a fibrous lesion of immature bone, with an incidence of 10–20% in the head and neck region. Most cases are monostotic, but when a lesion occurs on the maxillofacial region and spreads to the surrounding bone, it is classified as
Kisho Ono, Norie Yoshioka, Yuki Kunisada, Tomoya Nakamura, Yuko Nakamura, Kyoichi Obata, Soichiro Ibaragi, Shogo Minagi, Akira Sasaki   +8 more
doaj   +1 more source

A Case Report of Polyostotic form of Fibrous Dysplasia: Imaging Features in Radiograph, Computed Tomography and Magnetic Resonance Imaging

Journal of Clinical and Biomedical Sciences, 2022
Fibrous dysplasia is a disease that causes aberrant development of osteoblasts, which results in fibrous stroma replacing normal bone. Lichtenstein first described it in 1938. It is a sporadic disorder caused due to a postzygotic mutation in the
R B Revanth, Deepti Naik, Anil Kumar Sakalecha, . Aashish, Yashas Ullas, Guru M Yogendra   +5 more
doaj   +1 more source

Polyostotic Fibrous Dysplasia [PDF]

Proceedings of the Royal Society of Medicine, 1949
Summary A case of polyostotic fibrous dysplasia in a 5-year-old girl is reported. The diagnosis was made by the characteristic triad of predominantly unilateral bone lesions, precocious “puberty,” and unilateral skin pigmentation, and was substantiated by radiographic and pathologic examination of the bone lesions. The early onset of menses (second
L J, HACKETT, W M, CHRISTOPHERSON
openaire   +4 more sources