Results 21 to 30 of about 1,923 (160)

Osteochondroma of rib cage in a case of HME: A rare presentation

Journal of Orthopaedic Reports, 2023
Background: Osteochondroma is the most common benign bone tumor. This aberrant developmental lesion of the bone in the rib is rare and forms part of multiple diaphyseal aclasia in some cases.
Saroj prasad Sah, Vikas Maheshwari, Aditya K.S. Gowda, Bom Bahadur, Robin Yadav, Mohit Dhingra   +5 more
doaj   +1 more source

Spinal Exostosis in a Boy with Multiple Hereditary Exostoses

Case Reports in Orthopedics, 2013
We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal.
Ali Al Kaissi, Rudolf Ganger, Klaus Klaushofer, Franz Grill   +3 more
doaj   +1 more source

Osteochondroma of Upper Dorsal Spine Causing Spastic Paraparesis in Hereditary Multiple Exostosis: A Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2015
Osteochondroma of the spine is rare. It may present in solitary or multiple form (hereditary multiple exostoses). Herein, we report a case of an 18-year-old male who was diagnosed with thoracic osteochondroma, originating from the D4 vertebra with ...
Gaurav Kumar Upadhyaya, Vijay Kumar Jain, Rajendra Kumar Arya, Skand Sinha, Ananta Kumar Naik   +4 more
doaj   +1 more source

Reconstruction of the Hip in Multiple Hereditary Exostoses

Children, 2021
The hip joint involvement in multiple hereditary exostoses (MHE) occurs in 30–90%, causing pain and limitation of motion by femoroacetabular impingement, coxa valga, acetabular dysplasia, hip joint subluxation, and osteoarthritis.
Dong Hoon Lee, Dror Paley
doaj   +1 more source

Leveraging Point-Of-Care Ultrasound to Diagnose a Rare Arterial Occlusive Thrombus in a Child: A Case Study. [PDF]

J Clin Ultrasound
This case report illustrates the successful use of ultrasound imaging of arterial thrombosis in a child following orthopedic surgery, where regular diagnosis was difficult due to the presence of metallic orthopedic frames. ABSTRACT Pediatric arterial thromboembolism is an extremely rare and serious complication, especially rare when it is noncatheter ...
Ponde VC, Singh N, Johari AN, Smeds H, Boretsky K.   +4 more
europepmc   +2 more sources

Experience with arthroscopic treatment of disorders in the sternoclavicular joint: A prospective series of 78 patients

Knee Surgery, Sports Traumatology, Arthroscopy, EarlyView.
Abstract Purpose To evaluate pain, function and patient‐reported outcomes following arthroscopically intended treatment of painful sternoclavicular joint (SCJ) conditions between 2010 and 2024 in a consecutive cohort with long‐term follow‐up including 78 patients.
Anna Hoerby Normann Rasmussen, Martin Wyman Rathcke, Michael Rindom Krogsgaard   +2 more
wiley   +1 more source

Hereditary multiple exostoses with a giant osteochondroma degenerated into chondrosarcoma

Radiology Case Reports
We present a case of hereditary multiple exostoses with malignant transformation to chondrosarcoma in a woman complaining of enlargement and pain in the right thigh.
Federica Masino, MD, Manuela Montatore, MD, Rossella Carpentiere, MD, Marina Balbino, MD, Rossella Gifuni, MD, Giacomo Fascia, MD, Giuseppe Guglielmi, MD   +6 more
doaj   +1 more source

Hereditary Multiple Exostoses of the Hip

Journal of Orthopaedic Surgery, 2009
Purpose. To assess the radiographic features of 36 hips with hereditary multiple exostoses (HME). Methods. Hip parameters of 12 males and 6 females (36 hips) aged 2 to 28 years with HME were assessed using anteroposterior radiographs.
Tarek AM El-Fiky, Wang Chow, Yun Hoi Li, Michael To   +3 more
doaj   +1 more source

Congenital multiple exostoses with congenital heart disease

Medical Journal of Dr. D.Y. Patil University, 2017
Multiple exostoses are a rare disorder. It is estimated to occur in 1; 50,000 pregnancies. It presents within the first decade of life and it has an autosomal mode of inheritance; though it has been associated with a spontaneous mutation in 10% of cases.
Ibrahim Aliyu, Teslim O Lawal
doaj   +1 more source

Skeletal Dysplasia During the Bronze Age in Northeast Thailand (3000–2500 BP)

International Journal of Osteoarchaeology, EarlyView.
ABSTRACT This study examines a case of skeletal dysplasia in an adult male (B290) from the Bronze Age at the site of Ban Non Wat, Northeast Thailand. Skeletal dysplasia, a group of genetic disorders affecting bone and cartilage growth, presents diagnostic challenges due to overlapping clinical features.
Nuttheera Kaoboriboon, Nancy Tayles, Sarah Agatha Villaluz, Pratiwi Yuwono, Kate Domett, Melandri Vlok   +5 more
wiley   +1 more source