Results 51 to 60 of about 4,597 (202)
Clinical case of Gorham – Stoat syndrome
Сибирский научный медицинский журналDisappearing bone disease, or Gorham – Stoat syndrome, is a disease of massive osteolysis associated with the proliferation of hemangiotic tissue leading to bone resorption. Material and methods.
P. G. Shnyakin +4 more
doaj +1 more source
Chronic inflammation triggered by the NLRP3 inflammasome in myeloid cells promotes growth plate dysplasia by mesenchymal cells [PDF]
, 2017 Skeletal complications are common features of neonatal-onset multisystem inflammatory disease (NOMID), a disorder caused by NLRP3-activating mutations. NOMID mice in which NLRP3 is activated globally exhibit several characteristics of the human disease ...
Abu-Amer, Yousef +8 more
core +2 more sources
Characterization of Enhanced UHMWPE‐Hap Composites Manufactured by Hot Pressing
Polymer Composites, Volume 46, Issue 16, Page 15102-15114, 10 November 2025.Illustration of the production and examination of prepared composite samples. ABSTRACT In the present study, a hip joint cup/liner material has been developed using ultra high molecular weight polyethylene (UHMWPE) matrix material which is reinforced by hydroxyapatite (HAp) particles with the 0.5, 1, 2, and 4 wt.% using mechanical activation followed ...
Gözde Çelebİ Efe +4 more
wiley +1 more source
Gorham′s Massive Osteolysis - A Rare Case Report
Journal of Indian Academy of Oral Medicine and Radiology, 2006 Massive osteolysis is well known by the synonyms vanishing bone disease, phantom bone disease. First case ever reported was by Jackson in 1838 and later in 1972 in a patient with disappearing humerus. Romer in 1924 reported first case in the jaws.
Mangala Meti +2 more
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Gorham-Stout disease of the malleolus: a rare case report
BMC Musculoskeletal Disorders, 2019 Background Gorham-Stout disease, also known as vanishing bone disease, idiopathic massive osteolysis, is a rare entity of unknown etiopathology. This disease is characterized by destruction of osseous matrix and proliferation of lymphatic vascular ...
Chuanxi Zheng +6 more
doaj +1 more source
Biological response to prosthetic debris. [PDF]
, 2015 Joint arthroplasty had revolutionized the outcome of orthopaedic surgery. Extensive and collaborative work of many innovator surgeons had led to the development of durable bearing surfaces, yet no single material is considered absolutely perfect ...
Bitar, Diana, Parvizi, Javad
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Journal of Experimental Orthopaedics, Volume 12, Issue 4, October 2025.Abstract Purpose The combined use of reconstruction rings and modular trabecular metal (TM) augments can be a viable individual treatment in selected patients with large severe acetabular bone defects. However, clinical data on the outcome of this surgical technique is limited.
David Spranz +6 more
wiley +1 more source
Gorham disease involving the maxillofacial bones: A perplexing entity
Radiology Case Reports, 2018 Gorham disease is a rare disorder with progressive osteolysis which leads to the vanishing of bones. Its etiology and ideal management strategy are still an enigma. A case of Gorham disease involving the maxillofacial region in a 25-year-old male with an
Festi Lova, BDS, MHA +5 more
doaj +1 more source
Multicentric Disappearing Bone Disease treated with Arthroplasty [PDF]
Malaysian Orthopaedic Journal, 2016 Multicentric disappearing bone disease, or Gorham disease, is a rare entity. A middle age woman, presented to us with left sided antalgic gait and severe bony deformity of her left knee.
Chan CK +3 more
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Gorham's disappearing bone disease: a rare cause of extensive bone destruction [PDF]
, 2016 Osteolytic disease of the bones have a myriad range of aetiology. One rare cause is Gorham’s disease or disappearing bone disease. This disease is a diagnosis by exclusion using correlation made with clinical presentation, radiological findings and ...
Muridan, Roziah, Suppiah, Subapriya
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