Results 91 to 100 of about 9,014 (240)

Cervical Myelopathy Due to an Osteochondroma in Multiple Hereditary Exostosis

open access: yesCase Reports in Orthopedics, Volume 2026, Issue 1, 2026.
Hereditary multiple exostosis is a rare genetic condition characterized by the development of multiple exostoses. Vertebral localization is rare, less than 7%. Spinal cord compression in hereditary multiple exostosis is a rare condition. We report the case of a 22‐year‐old man with cervical spinal cord compression due to an osteochondroma with ...
Géraud Garcia Segbedji   +4 more
wiley   +1 more source

Identification of a rare case of intra-articular osteochondroma manifesting as three loose bodies in a patient with hereditary multiple osteochondromas: A case report.

open access: yesOncology Letters, 2015
Hereditary multiple osteochondromas (HMO) is an autosomal dominant bone disorder characterised by the presence of multiple benign cartilage-capped tumours.
Mingxiang Kong   +9 more
semanticscholar   +1 more source

[Osteochondromas: introducing the subungual osteochondroma].

open access: yesActa ortopedica mexicana, 2019
Subungual osteochondromas are benign tumors of the sub- or periungual region, causing lifting, ulceration and deformity at that level.To research the incidence of subungual osteochondromas in a specific pediatric population.Retrospective, transversal, descriptive and observational study based on the review of records with a histopathological result of ...
F, Tamayo-Pacho   +4 more
openaire   +1 more source

Uncommon Presentation of a Rib Osteochondroma Misdiagnosed as a Breast Lesion: A Case Report

open access: yesCase Reports in Orthopedics, Volume 2026, Issue 1, 2026.
Case Osteochondromas are common benign bone tumors. Rarely, these lesions present on the ribs and can be concerning for a breast mass. This case discusses a healthy 21‐year‐old female with a firm, fixed, painful breast mass. Her initial ultrasound and 6‐month follow‐up ultrasound were both benign.
Bailey R. Abernathy   +5 more
wiley   +1 more source

Solitary Osteochondroma of the Skull Base: A Case Report and Literature Review

open access: yesJournal of Neurological Surgery Reports, 2015
We report a case of an osteochondroma in the posterior clinoid process that occurred in a 43-year-old man with trochlear nerve palsy. Although the potential preoperative diagnoses based on computed tomography and magnetic resonance imaging included other
Hiroki Hongo   +3 more
doaj   +1 more source

Radiological conference. Enchondroma [PDF]

open access: yes, 1998
published_or_final_versio
Peh, WCG, Wong, LLS
core  

Regression of a solitary osteochondroma of the distal humerus in a toddler following trauma

open access: yesRadiology Case Reports, 2019
Osteochondromas are bone exostoses, with the vast majority extending from the metaphyseal region of long bones and are capped by cartilage. A review of the current literature reveals spontaneous regression of osteochondromas is a rarely documented event,
Paul B. Heyworth, MBBS   +1 more
doaj   +1 more source

Osteocondroma de apófisis coronoides [PDF]

open access: yes, 2006
El osteocondroma es la neoplasia benigna más común del esqueleto. En la cabeza se ha descrito su localización en base de cráneo, cara posterior del maxilar, senos maxilares, y en diferentes áreas de la mandíbula, como cóndilo, rama, cuerpo y región ...
Cornejo, Marco   +4 more
core   +1 more source

Multiple exophytic osteomas of craniofacial bones not associated with Gardner s Syndrome: a case report [PDF]

open access: yes, 2004
Exophytic osteomas are mature bone protuberances required to be carefully differentiated from other lesions. The authors present a male, 44 year-old patient s report presenting multiple exophytic osteomas located in both sides of the vestibulomaxillary ...
Mazzoni, Alessandra   +3 more
core   +4 more sources

Haplotype Construction Using Embryos as Probands of the Pathogenic Variations in EXT1, CUL3, and HBA

open access: yesHuman Mutation, Volume 2026, Issue 1, 2026.
Preimplantation genetic testing (PGT) represents a crucial strategy in the prevention of monogenic disorders, ensuring that only embryos free from these genetic conditions are implanted during assisted reproductive technologies. By analyzing the type of haplotypes of the variation of the probands or the carriers, we can significantly enhance the ...
Defeng Shu   +5 more
wiley   +1 more source

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