Results 1 to 10 of about 1,261 (184)

A rare case of hereditary multiple osteochondromas [PDF]

The Pan African Medical Journal, 2020
Five (5) years old male patient came to outpatient department with complain of multiple swelling over chest region with upper extremities. The clinical examination revealed that there is chest multiple mass growth of about 3-4 cm bilaterally each over ...
Rakesh Khatana, Renu Rathi
doaj   +5 more sources

Osteosarcoma Arising from Iliac Bone Lesions of Hereditary Multiple Osteochondromas: A Case Report [PDF]

Case Reports in Oncology
Introduction: Osteochondromas are benign tumors that arise primarily in the metaphyseal region of long bones. The malignant transformation rate is estimated to be less than 1% and 1–3% in solitary and multiple osteochondromas, respectively ...
Tadamasa Handa, Kunihiro Asanuma, Hiroto Yuasa, Tomoki Nakamura, Tomohito Hagi, Katsunori Uchida, Akihiro Sudo   +6 more
doaj   +4 more sources

Spinal cord stimulation for treatment of the pain associated with hereditary multiple osteochondromas [PDF]

Journal of Pain Research, 2015
Ravi G Mirpuri,1 Jereme Brammeier,2 Hamilton Chen,2 Frank PK Hsu,1,3 Vi K Chiu,4 Eric Y Chang1,2,5 1Department of Physical Medicine and Rehabilitaiton, 2Department of Anesthesiology and Perioperative Care, 3Department of Neurological Surgery, 4Department
Mirpuri RG, Brammeier J, Chen H, Hsu FP, Chiu VK, Chang EY   +5 more
doaj   +9 more sources

Hereditary multiple osteochondromas

Portuguese Journal of Pediatrics
A three-year-old boy’s mother reports the appearance of painless swelling at the right tibia’s proximal end, with one year of evolution, without previous trauma or local/systemic inflammatory signs, namely fever or lymphadenopathy.
João R. Nunes-Pires, Violeta Florova, Teresa Alves-da Silva   +2 more
doaj   +4 more sources

Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas. [PDF]

Turk Arch Pediatr, 2023
Hereditary multiple osteochondromas is an autosomal dominant disorder caused by heterozygous pathogenic variants in EXT1 or EXT2. We aimed to evaluate the clinical and molecular findings of a Turkish cohort with hereditary multiple osteochondroma.Thirty-two patients aged 1.3-49.6 years from 22 families were enrolled.
Güneş N, Uludağ Alkaya D, Toylu A, Özüdoğru P, Çifçi Sunamak E, Şeker A, Demir B, Kuruğoğlu S, Mıhçı E, Tüysüz B.   +9 more
europepmc   +4 more sources

Modified osteotomy for treatment of forearm deformities (Masada IIb) in hereditary multiple osteochondromas: a retrospective review [PDF]

BMC Musculoskeletal Disorders, 2021
Purpose Approximately 30% of patients with hereditary multiple osteochondromas (HMO) have forearm deformity and dysfunction. The aim of this retrospective study was to review our experience with the surgical treatment of children with HMO and Masada IIb ...
Ge Yan, Guoxin Nan
doaj   +2 more sources

Biplanar EOS screening in children with hereditary multiple osteochondromas: a feasible screening method? [PDF]

Frontiers in Pediatrics
BackgroundChildren with Hereditary Multiple Ostechondromas (HMO) require regular screening to identify gradual dysplasia or osteochondromas that need surgery.
Henrik Hedelin, Henrik Hedelin, Jenny Ahlin, Jenny Ahlin, Aina Danielsson, Aina Danielsson, Helena Brisby, Helena Brisby, Kerstin Lagerstrand, Kerstin Lagerstrand   +9 more
doaj   +2 more sources

Arthroscopic Anterior Cruciate Ligament Reconstruction in a 17-Year-Old Female Athlete with Multiple Hereditary Exostoses Using a Peroneus Longus Autograft: A Rare Case Report [PDF]

Journal of Orthopaedic Case Reports
Introduction: Hereditary multiple exostoses, also known as multiple osteochondromas, is a rare genetic disorder marked by the formation of osteocartilaginous outgrowths predominantly near the metaphysis of long bones.
Sanjay Singh Chauhan, Harshita Udiwal, Narendra Singh Butola   +2 more
doaj   +2 more sources

Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas. [PDF]

Ther Clin Risk Manag, 2017
Hereditary multiple osteochondromas (HMO), previously named hereditary multiple exostoses (HME), is an autosomal dominant skeletal disorder characterized by the growth of multiple osteochondromas and is associated with bony deformity, skeletal growth reduction, nerve compression, restriction of joint motion, and premature osteoarthrosis.
Akbaroghli S, Balali M, Kamalidehghan B, Saber S, Aryani O, Meng GY, Houshmand M.   +6 more
europepmc   +6 more sources

Treatment of multiple hereditary osteochondromas of the forearm in children [PDF]

Journal of Bone and Joint Surgery: British Volume, 2006
We have evaluated the clinical outcomes of simple excision, ulnar lengthening and the Sauvé-Kapandji procedure in the treatment of deformities of the forearm in patients with multiple hereditary osteochondromas. The medical records of 29 patients (33 forearms) were reviewed; 22 patients (22 forearms) underwent simple excision (four with ulnar ...
E K, Shin, N F, Jones, J F, Lawrence
exaly   +3 more sources