Results 51 to 60 of about 4,389 (174)

Bilateral osteochondroma in a child: A rare case report

Journal of Bone and Joint Diseases
Osteochondroma has an incidence of 1 in 50,000 and is the most common benign bone tumor, which accounts for 30% (range 20%–50%) of all benign bone tumors. The incidence of osteochondroma is higher in males than females in both its solitary and hereditary
Abhishek Kumar, Sarthak Das, Saroj Kumar Tripathy, Archana Malik   +3 more
doaj   +1 more source

Physiotherapist's Management of Suspected Cauda Equina Syndrome in the United Kingdom: A National Survey

Physiotherapy Research International, Volume 31, Issue 2, April 2026.
ABSTRACT Background and Purpose Cauda Equina Syndrome (CES) is a rare but serious spinal condition requiring urgent diagnosis and management. Physiotherapists in UK musculoskeletal (MSK) services increasingly encounter suspected CES cases, but little is known about their clinical decision‐making and referral practices.
Rob Tyer, Nick Livadas, Robert Hogg
wiley   +1 more source

Endoscopic Resection of Bizarre Parosteal Osteochondromatous Proliferation of the Calcaneocuboid Joint

Arthroscopy Techniques, Volume 15, Issue 3, March 2026.
Abstract Bizarre parosteal osteochondromatous proliferation (BPOP), or Nora's lesion, is an unusual, benign, parosteal lesion comprising bone, fibrous tissue, and cartilage. Clinically, the lesions present as slowly growing hard protuberances that are painless in most cases unless they cause local symptoms due to mass effect, including pain, palpable ...
Tun Hing Lui, Kit Leung
wiley   +1 more source

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

Developmental Dynamics, Volume 255, Issue 3, Page 228-245, March 2026.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki, Rinna Kanai, Sayuri Tatsuta, Shinichi Kawaguchi, Masatsune Itoh, Shinsuke Ohba, Makoto Abe   +6 more
wiley   +1 more source

Primary Chest Wall Ewing Sarcoma With Diaphragmatic Invasion in an Adult: En‐Bloc Resection and Polypropylene Mesh Reconstruction

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Chest‐wall Ewing sarcoma (CWES) is uncommon in adults and often abuts vital thoracic structures, making R0 resection challenging despite gains with multimodal therapy. A 46‐year‐old Arab male presented with year‐long right‐sided chest pain, weight loss, and a firm mass over the lower right ribs.
Mohammad Alaa Aldakak, Ahmad Al‐Bitar, Raneem Ahmad, Hamza Alhallaq, Kinda Assoud, Hussain Chaban   +5 more
wiley   +1 more source

The Application of Orthopedic Surgical Robot‐Assisted Technology in Various Clinical Scenarios Involving Bone Tumors

Orthopaedic Surgery, Volume 18, Issue 1, Page 53-65, January 2026.
Robot‐assisted surgery facilitates precise path planning and osteotomy plane identification. With the combination of an orthopedic robot and intraoperative ultrasound or the da Vinci robot, it can enhance the precision and safety of bone tumor surgery. Furthermore, it can be integrated with patient‐specific cutting guides to minimize surgical duration.
Hanxiao Yin, Yiwei Fu, Xirenijiang Yikemu, Weihai Liu, Changye Zou, Xianbiao Xie, Zhiqiang Zhao, Puyi Sheng, Jingnan Shen, Junqiang Yin   +9 more
wiley   +1 more source

Suspected Calvarial Hyperostosis Syndrome Causing Different Ophthalmological Signs in Two Young Labrador Retrievers—Case Report

Veterinary Ophthalmology, Volume 29, Issue 1, January 2026.
ABSTRACT Objective To describe calvarial hyperostosis syndrome (CHS) as a potential and unusual cause of exophthalmos or epiphora in young dogs. Animals Studied A nine‐month‐old female intact (case 1) and a two‐year‐old male intact Labrador Retriever (case 2). Procedures Patient history, including previous treatments, was documented.
Andrea Steinmetz, Stefan Kohl
wiley   +1 more source

Multiple Osteochondromas: Clinicopathological and Genetic Spectrum and Suggestions for Clinical Management

Hereditary Cancer in Clinical Practice, 2004
Multiple Osteochondromas is an autosomal dominant disorder characterised by the presence of multiple osteochondromas and a variety of orthopaedic deformities.
Hameetman Liesbeth, Bovée Judith VMG, Taminiau Antonie HM, Kroon Herman M, Hogendoorn Pancras CW   +4 more
doaj   +1 more source

Spontaneous resolution of a solitary osteochondroma of humerus following trauma: A case report with a review of literature

Journal of Orthopaedics, Trauma and Rehabilitation, 2019
Osteochondroma is the most common benign bone tumor; however, the natural history of the lesion is still poorly understood. Symptomatic osteochondromas are treated with excision, but more often the indications are mainly cosmetic or fear of malignant ...
Jalan Divesh, Lam Ying Lee, Wong Joyce, Yau Ching Hin Raymond   +3 more
doaj   +1 more source

Trigger finger due to phalangeal osteochondroma of an adult: A case report

Journal of Orthopaedic Surgery, 2020
Trigger finger is stenosing tenosynovitis that occurs in A1 pulley. It usually occurs idiopathically in patients’ 40s and 50s. On the other hand, pediatric trigger finger usually occurs before 8 years old in pediatric patients.
Hoi Young Kwon, Hong Je Kang
doaj   +1 more source