Results 21 to 30 of about 30,224 (246)
Plexiform Fibrohistiocytic Tumour at a Rare Site: Frontal Region of Head with underlying Frontal Bone Invasion [PDF]
Journal of Clinical and Diagnostic Research, 2022 Plexiform Fibrohistiocytic Tumour (PFHT) is an intermediate malignant tumour of soft tissue. It is a rarely metastasising dermal subcutaneous neoplasm. It affects children and young adults. The age range of presentation is from birth to age 77 years. The
Sarita Nibhoria +4 more
doaj +1 more source
, 2014 From 1982 to 1987, 4 cases with giant cell tumour of bone surgically treated in our clinic are presented. Tumor localizations were at talus, distal radial edge, proximal humeral edge and distal femoral metaphysis respectively. Two cases treated with curettage, and grafting and the other two received local resection and grafting.
HUNER, Hakan +3 more
+5 more sources
Use of Denosumab in Children With Osteoclast Bone Dysplasias: Report of Three Cases. [PDF]
, 2019 Denosumab has been used successfully to treat disease-associated osteoclast overactivity, including giant cell tumor of bone. Given its mechanism of action, denosumab is a potent potential treatment of other osteoclast bone dysplasias including central ...
Bernthal, Nicholas M +8 more
core +2 more sources
Trauma Case Reports, 2019 Background: Giant cell tumours are common primary long bone tumours with femoral neck locations infrequent and notorious for pathological fractures. Treatment with simple curettage often results in local recurrence.
S. Abdulrazak +4 more
doaj +1 more source
Grade 3 Giant Cell Tumour of the Distal Humeral Epiphysis Treated with Intralesional Curettage, High Speed Burring and Bone Grafting: A Case Report [PDF]
Malaysian Orthopaedic Journal, 2022 Giant cell tumours of bone are benign but locally aggressive neoplasms involving the epi- and metaphysis of long bones. Tumours of the distal humeral epiphysis with cortical disruption and invasion into the joint and the soft tissues are rare and ...
Nyffeler RW, Ziebarth K
doaj +1 more source
A chondroblastic osteosarcoma of the coronoid process mimicking a fragmented coronoid process in a dog [PDF]
, 2016 A 6-year-old Rhodesian Ridgeback was presented with a 1.5 year history of right forelimb lameness. Clinical, radiological and computed tomographic findings suggested the presence of fragmented medial coronoid process.
Cirkel, Koen +4 more
core +1 more source
Soft Tissue Giant Cell Tumour of Low Malignant Potential: A Rare Tumour at a Rare Site [PDF]
Journal of Clinical and Diagnostic Research, 2013 “Soft tissue giant cell tumour of low malignant potential” is considered as the soft tissue counterpart of osteoclastoma of the bone. It is a primary soft tissue tumour which is classified under the category of fibrohistiocytic tumours of intermediate ...
Amoolya Bhat, Geethamani V., Vijaya C.
doaj +1 more source
Molecular and cellular pathogenesis of adamantinomatous craniopharyngioma. [PDF]
, 2015 Adamantinomatous craniopharyngiomas (ACPs) are the most common pituitary tumours in children. Although histologically benign, these are clinically aggressive tumours, difficult to manage and associated with poor quality of life for the patients.
Martinez-Barbera, JP
core +1 more source
BMP2/BMPR1A is linked to tumour progression in dedifferentiated liposarcomas [PDF]
, 2016 Bone Morphogenic Protein 2 (BMP2) is a multipurpose cytokine, important in the development of bone and cartilage, and with a role in tumour initiation and progression.
Cassidy, A.P. +3 more
core +3 more sources
Acta Orthopaedica et Traumatologica Turcica, 2021 From 1982 to 1987, 4 cases with giant cell tumour of bone surgically treated in our clinic are presented. Tumor localizations were at talus, distal radial edge, proximal humeral edge and distal femoral metaphysis respectively.
Hakan Huner +3 more
doaj