Results 41 to 50 of about 1,132 (155)

Osteochondroma of the scapula associated with a subclavian artery pseudoaneurysm: Case report

SAGE Open Medical Case Reports, 2019
Osteochondromas rarely induce vascular complications by mechanical compression. We present the case of a subclavian artery pseudoaneursym caused by an osteochondroma of the scapula in a 67-year-old male.
Ana Oljaca, Daniela Hirzberger, Marko Bergovec, Kurt Tiesenhausen, Stephan H Koter, Joerg Friesenbichler, Christian Viertler, Andreas Leithner   +7 more
doaj   +1 more source

Hip Joint Osteochondroma: Systematic Review of the Literature and Report of Three Further Cases

Advances in Orthopedics, 2014
The aim of this study is to systematically review the literature with regards to surgical treatment of patients with hip joint osteochondromas, and to report our surgical management of three paediatric patients who had femoral neck or acetabular ...
Asim M. Makhdom, Fan Jiang, Reggie C. Hamdy, Thierry E. Benaroch, Martin Lavigne, Neil Saran   +5 more
doaj   +1 more source

High‐Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient‐Reported Data

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 1989-1999, September 2026.
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George, Bamelak T. Duki, Zoe S. Katz, Aravind Viswanathan, Suzanne P. MacFarland, Evan R. Hathaway, Caitlin Monahan, John Morris, Kelly L. Trout, Shari M. Krantz, Arupa Ganguly, Jennifer M. Kalish   +11 more
wiley   +1 more source

Orthopedic preoperative evaluation and surgical strategies of hereditary multiple osteochondromas involving the spinal region

EFORT Open Reviews
Hereditary multiple osteochondromas (HMO), previously known as hereditary multiple exostoses (HME), is a congenital skeletal developmental anomaly characterized by multiple osteochondromas that commonly grow outward from the metaphyses of long bones ...
Shuzhong Liu, Jinyi Xing, An Song, Xi Zhou, Yong Liu   +4 more
doaj   +1 more source

Popliteal artery pseudoaneurysm caused by non–penetrating trauma in a patient with hereditary multiple osteochondromatosis

Radiology Case Reports, 2022
Hereditary multiple osteochondromatosis is a genetic condition characterized by the appearance of numerous osteochondromas, which can cause pseudoaneurysms in rare cases.
Oscar Andrés Parada Duarte, MD, Juan Guillermo Arámbula Neira, MD, Valeria del Castillo Herazo, MD, María Fernanda Oviedo Lara, MD, Adriana Lucía López Polanco, MD, Andrés Felipe Durán Omaña, MD, Andrés Felipe Herrera Ortiz, MD   +6 more
doaj   +1 more source

Chronic Pain as an Early Diagnostic Clue in Hereditary Multiple Exostoses: Two Pediatric Cases Highlighting Diagnostic Delay

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Hereditary multiple exostoses (HME) is a rare autosomal dominant skeletal disorder characterized by the development of multiple osteochondromas adjacent to the growth plates. Although skeletal deformities and palpable masses are common findings, chronic pain may represent an early and underappreciated diagnostic clue, particularly in pediatric
Melissa Mariti Fraga, Valesca Oliveira Paes Tanaka, Luciana Tudech Salgueiro Pedro Paulo, Maria Carolina Santos, Carolina Costa Figueiredo, Nara Michelle de Araújo Evangelista, Vânia de Fátima Tonetto Fernandes, Guido de Paula Colares Neto   +7 more
wiley   +1 more source

Hereditary Multiple Exostoses with Ulnar Hemimelia

Proceedings, 2021
Hereditary Multiple Exostoses is a skeletal dysplasia that is very rare and defined by formation of numerous cartilage capped benign tumours either pedunculated or sessile known as osteochondromas throughout skeleton especially around the growth plates ...
Syed Wasif Ali Shah, Muhammad Abdul Shakoor, Usman Amjad, Haider Ali, Waleed Imtiaz, Shafqat Raza   +5 more
doaj   +1 more source

Examining the Role of Artificial Intelligence in Assessment: A Comparative Study of ChatGPT and Educator‐Generated Multiple‐Choice Questions in a Dental Exam

European Journal of Dental Education, Volume 30, Issue 3, Page 881-895, August 2026.
ABSTRACT Aim To compare the item difficulty and discriminative index of multiple‐choice questions (MCQs) generated by ChatGPT with those created by dental educators, based on the performance of dental students in a real exam setting. Materials and Methods A total of 40 MCQs—20 generated by ChatGPT 4.0 and 20 by dental educators—were developed based on ...
Nezaket Ezgi Özer, Yusuf Balcı, Gaye Bölükbaşı, Betul İlhan, Pelin Güneri   +4 more
wiley   +1 more source

Rapidly acquired valgus deformity of the knee after osteochondroma resection in multiple hereditary exostoses pediatric patients: A report of two cases

Radiology Case Reports, 2022
Patients with multiple hereditary exostoses (MHE) often develop leg length discrepancies and limb alignment deformity around the knee as part of the natural course of the disease. Limb alignment deformity occurring post-resection of an osteochondroma has
Alexandra H. Aitchison, BS, David Alcoloumbre, MD, Ana C. Belzarena, MD, John S. Blanco, MD   +3 more
doaj   +1 more source

A Dialogic Participatory Model Between Professionals and Patients for the Co‐Creation of Transitioning Care Management Programmes in Rare Bone Diseases

Health Expectations, Volume 29, Issue 4, August 2026.
ABSTRACT Introduction Rare diseases are a group of heterogeneous conditions affecting fewer than 5 per 10,000 individuals in Europe, with rare bone diseases representing a clinically significant subgroup. Multiple osteochondromas, Ollier disease and Maffucci syndrome are multifocal benign rare disorders, characterised by bone deformities, functional ...
Marina Mordenti, Silvia Forni, Eleonora Grippa, Maria Cecilia la Forgia, Davide Scognamiglio, Manila Boarini, Gabriella Massa, Andrea Romeo, Alessandro Sergi, Luca Sangiorgi, Transitioning Care Management Working Group (TCM WG), Giovanni Beltrami, Domenico Campanacci, Nunzio Catena, Mauro Celli, Marta Cervo, Leonardo D'Agruma, Gian Luigi Federico, Giovanni Gallone, Michela Veronika Gonfiantini, Laura Masi, Maria Beatrice Michelis, Osvaldo Palmacci, Annabruna Ronchetti, Paolo Trezza   +24 more
wiley   +1 more source