Results 11 to 20 of about 4,597 (202)

Pseudomyogenic Hemangioendothelioma of the Femur Treated by Intercalary Resection and Massive Allograft Reconstruction: A Case Report. [PDF]

Case Rep Orthop
Pseudomyogenic hemangioendothelioma (PHME) is a very rare vascular tumor that usually arises in the extremities, mainly cutaneous or subcutaneous, but also occurs in deeper locations, such as muscles and bone. Less than 200 cases have been reported so far, and primary intraosseous PHMEs are further infrequent.
Martín Cocilova FN, Neri E, Nozzoli F, Tatti T, Palomba A, Roselli G, Campanacci DA.   +6 more
europepmc   +2 more sources

Early mobilisation versus delayed protocols after reverse total shoulder arthroplasty for nonfracture indications: A systematic review and meta-analysis. [PDF]

J Exp Orthop
Abstract Purpose This study aimed to compare clinical outcomes, range of motion, pain scores and complication rates between early and delayed mobilisation following reverse total shoulder arthroplasty (RTSA). Methods A systematic review and meta‐analysis were conducted according to 2020 Preferred Reporting Items for Systematic Reviews and Meta‐Analyses
Thamrongskulsiri N, Itthipanichpong T, Kongmalai T, Kongmalai P.   +3 more
europepmc   +2 more sources

Pelvic pseudotumor following total hip arthroplasty. Case report

Journal of the Bulgarian Orthopaedics and Trauma Association, 2023
According to the literature, the development of metallosis after hip arthroplasty occurs in approximately 5% of patients. Metallic debris in the joint results in massive local and systemic release of cytokines. Excision of the pelvic pseudotumor, as well
Luben Stokov, Elka Angelova, Asen Todorov, Georgi Georgiev   +3 more
doaj   +3 more sources

Surgical treatment of severe thoracic kyphosis and neurological deficit in a patient with Gorham–Stout syndrome: A case report and literature review

Frontiers in Surgery, 2022
BackgroundGorham–Stout syndrome is an uncommon condition with a varied clinical presentation and unclear cause that is characterised by a proliferation of lymphatic capillaries and severe regional osteolysis. Spinal and visceral involvement increases the
Hanwen Zhang, Chaofan Han, Daming Pang, Hai Yong, Jincai Yang, Peng Yin, Lijin Zhou   +6 more
doaj   +1 more source

Gorham-Stout Disease with Multiple Bone Involvement—Challenging Diagnosis of a Rare Disease and Literature Review

Medicina, 2021
Gorham-Stout disease is a rare disorder, which may result in a poor prognosis. This disease, a rare lymphangiomatosis, is defined by progressive bone disappearance due to massive unicentric and multicentric osteolysis. Osteolytic lesions of the spine and
Alina Momanu, Lavinia Caba, Nicoleta Carmen Gorduza, Oana Elena Arhire, Alina Delia Popa, Victor Ianole, Eusebiu Vlad Gorduza   +6 more
doaj   +1 more source

Radiotherapy in langerhans cell histiocytosis : a rare indication in a rare disease [PDF]

, 2013
Introduction: Langerhans Cell Histiocytosis (LCH) represents a rare benign disorder, previously designated as "Histiocytosis X", "Type II Histiocytosis" or "Langerhans Cell Granulomatosis".
Bruns, Frank, Büntzel, Jens, Eich, Hans Theodor, Haverkamp, Uwe, Heyd, Reinhard, Kriz, Jan, Micke, Oliver, Schäfer, Ulrich, Seegenschmiedt, Heinrich   +8 more
core   +3 more sources

Lymphangiomatosis of the arm with massive osteolysis. A case report. [PDF]

, 1987
A case of massive osteolysis of the arm is described where the typical bony lesions were associated with soft tissue ...
Ceciliani L., Mora R, Pazzaglia UE
core   +1 more source

Molecular dissection of the mechanism by which EWS/FLI expression compromises actin cytoskeletal integrity and cell adhesion in Ewing sarcoma. [PDF]

, 2014
Ewing sarcoma is the second-most-common bone cancer in children. Driven by an oncogenic chromosomal translocation that results in the expression of an aberrant transcription factor, EWS/FLI, the disease is typically aggressive and micrometastatic upon ...
Beckerle, Mary C, Chaturvedi, Aashi, Grossmann, Allie H, Hoffman, Laura M, Jensen, Christopher C, Lessnick, Stephen L, Lin, Yi-Chun, Randall, R Lor, Welm, Alana L   +8 more
core   +1 more source

Massive osteolysis in an infant [PDF]

American Journal of Roentgenology, 1980
Idiopathic dissolution of bone may occur in association with hemangiomatosis [1 , 2] or nephropathy [3]. It may be localized to a specific region of the body as in hereditary tarsal and carpal osteolysis [4]. When dissolution occurs without associated findings, it is called Gorhams osteolysis or massive osteolysis.
J, Abrahams, D, Ganick, E, Gilbert, J, Wolfson   +3 more
openaire   +2 more sources

Vanishing (Disappearing) Bone Disease in children: a review [PDF]

, 2011
Vanishing bone disease is a very rare, peculiar destructive condition of the skeletal system resulting in spontaneous and progressive resorption and disappearance of osseous structures with replacement by vascular, fibrous connective tissue.
Nagaveni, N.B., Radhika, N.B., Satisha, T.S., Umashankara, K.V.   +3 more
core   +1 more source