Time-lapse technic used to uncover the naturel growth of osteochondromas of the wrist in patients with Hereditary Multiple Osteochondromas [PDF]
, 2017 Background: In patients with Hereditary Multiple Osteochondromas (HMO) shortening and deformity of the long bones is a well-known sequel. Several theories could clarify the cause of shortening or deformity.
Derwall, John +7 more
core +2 more sources
Differentiation of Pediatric Osteochondroma From Trevor's Disease and Successful Surgical Management: A Case Report. [PDF]
Case Rep OrthopOsteochondroma is the most common benign bone tumor; however, its presentation in the small bones of the appendicular skeleton, particularly the talus and subtalar joint, is quite rare. Although most cases of osteochondroma are asymptomatic, symptomatic presentations can lead to joint deformity, pain, swelling, tarsal tunnel syndrome, gait alterations,
Montalbano A +3 more
europepmc +2 more sources
In Situ Hybridization of Feline Leukemia Virus in a Case of Osteochondromatosis
Veterinary Sciences, 2022 Osteochondromatosis, also known as multiple cartilaginous exostosis, polyostotic osteochondroma, and multiple osteochondromas, comprises one-fifth of all primary bone tumors in cats, with no breed or sex predisposition or hereditary pattern.
Anna Szilasi +4 more
doaj +1 more source
Proximal clavicular osteochondroma: A report of an unusual site
Journal of Pediatric Surgery Case Reports, 2022 Background: Osteochondromas are benign surface tumors that comprise a large sum of all bone tumors. They can present as solitary lesions or part of a collective such as in hereditary multiple osteochondromas (HMO).
Motaip H. Alrawili +3 more
doaj +1 more source
An unusual diagnosis for an usual test
Italian Journal of Pediatrics, 2020 Background Hereditary multiple osteochondromas (HMO) is a genetic condition characterized by the presence of multiple osteochondromas, usually at the lateral side of the most active growth plate of a long bone.
Andrea Trombetta +4 more
doaj +1 more source
Frontiers in Genetics, 2021 Hereditary multiple exostoses (HMEs) syndrome, also known as multiple osteochondromas, represents a rare and severe human skeletal disorder. The disease is characterized by multiple benign cartilage-capped bony outgrowths, termed exostoses or ...
Ewelina Bukowska-Olech +9 more
doaj +1 more source
Acute Cervical Myelopathy from Hereditary Multiple Exostoses: Case Report [PDF]
, 1989 A case of hereditary multiple exostoses with acute cervical myelopathy, tetraplegia, and apnea is reported. Neurological complications as a result of osteochondromas in hereditary multiple exostoses are rare.
Dennis Y. Wen +2 more
core +1 more source
Intraosseous Atypical Chondroid Tumor or Chondrosarcoma Grade 1 in Patients with Multiple Osteochondromas [PDF]
, 2015 Background: The autosomal dominant condition multiple osteochondromas, formerly called multiple hereditary exostoses, is associated with a risk of malignant progression of osteochondroma into secondary peripheral chondrosarcoma.
Ham, John +5 more
core +1 more source
Foramen magnum osteochondroma causing myelopathy in a patient with hereditary multiple exostoses [PDF]
Surgical Neurology International, 2020 Background: Osteochondromas are commonly occurring benign bone tumors which may be either a solitary lesion or occur due to association with hereditary multiple exostoses (HMEs). There have been several reported cases of spinal osteochondromas, but intracranial lesions are rare.
Sinha, Siddharth +2 more
openaire +2 more sources
Multiple hereditary exostoses: A pseudoaneurysm masquerading as tumor [PDF]
, 2016 Multiple hereditary exostoses is an autosomal dominant condition characterized by numerous benign osteochondromas. Complications are rare and can include deformity, growth abnormality, fracture, adventitial bursa formation, local mass effect on a nerve ...
Hari M Trivedi +9 more
core +1 more source