Results 11 to 20 of about 6,506 (215)

Truncated FOS impairs osteogenic differentiation and induces prostaglandin and NFκB signalling in an in vitro cell-of-origin model for osteoid osteoma and osteoblastoma. [PDF]

open access: yesJ Pathol
Abstract Osteoid osteoma and osteoblastoma are non‐malignant bone‐forming tumours of the skeleton, characterised by the presence of irregular trabeculae of woven bone. Rearrangements in FOS, and less frequently FOSB, have recently been identified in osteoid osteoma and osteoblastoma.
Lam SW   +10 more
europepmc   +2 more sources

Arthroscopic Excision of the Juxta-Articular Osteoid Osteoma From the Calcaneus at the Sinus Tarsi. [PDF]

open access: yesArthrosc Tech
Abstract Osteoid osteoma (OO) is a benign bone tumor that can rarely occur in the sinus tarsi, where its nonspecific symptoms may lead to delayed or incorrect diagnosis. When identified in this location, arthroscopic excision offers a minimally invasive and precise approach for management, although reports of its use remain limited.
Wróbel M   +3 more
europepmc   +2 more sources

A Case of Chronic Myeloid Leukemia Presenting with Osteoid Osteoma: A Diagnostic Dilemma

open access: yesAsian Pacific Journal of Cancer Care, 2021
Chronic myeloid leukemia is a hematological malignancy resulting from a clonal proliferation of hematopoietic stem cells of the myeloid series. It is developed by chromosomal translocation.
Mannavi Suman   +4 more
doaj   +1 more source

Osteoid osteoma.

open access: yesActa orthopaedica Belgica, 2006
Osteoid osteoma is a relatively frequent benign bone tumour, consisting of osteoid and woven bone, and surrounded by a halo of reactive sclerotic bone, with an average size of the nidus less than 1.5 cm. It is a condition of late childhood, adolescence and young adult age.
Kitsoulis, P.   +2 more
  +8 more sources

Intra cortical osteoid osteoma in distal radial metaphysis: A rare case report

open access: yesJournal of Orthopaedic Reports, 2023
Background: Osteoid osteoma of the lower end radius is a rare tumour with six reports available in the literature. Case report: A 18-year-old male presented with unexplained dorsal wrist pain.
V.K. Gautam   +3 more
doaj   +1 more source

Bone: Osteoblastoma [PDF]

open access: yes, 2010
Review on Bone: Osteoblastoma, with data on clinics, and the genes ...
de, Andrea CE, Hogendoorn, PCW
core   +1 more source

Osteoid osteoma near the intervertebral foramen may induce radiculopathy through tumorous inflammation

open access: yesDiagnostic Pathology, 2011
Osteoid osteoma of the spine is a relatively rare bone-forming tumor. Pain that is worse at night and relieved by aspirin and muscle contracture are the most characteristic symptoms of spinal osteoid osteoma.
Komiya Setsuro   +4 more
doaj   +1 more source

Osteoid Osteoma of the Occipital Condyle in Adolescents: Surgical Resection Under Navigation. [PDF]

open access: yesClin Case Rep
ABSTRACT This article reports a 12‐year‐old male with occipital condyle osteoid osteoma, presenting with neck pain and limited motion, unresponsive to conservative treatment. CT revealed a right condylar lesion. Surgical excision via a right paramedian suboccipital incision achieved complete recovery, confirmed by pathology and 3‐month follow‐up.
Li Y   +8 more
europepmc   +2 more sources

Osteoid osteoma—osteoblastoma [PDF]

open access: yesCancer, 1974
In view of the clinical and pathological similarities, osteoid osteoma and osteoblastoma can be considered variants of one benign osteoblastic process. We suggest classifying these lesions according to their location in the bone, for that location determines the nature of reaction evoked.
L, De Souza Diaz, H M, Frost
openaire   +2 more sources

A case of a femoral neck tumor: painless osteoid osteoma? [PDF]

open access: yes, 2005
We report herein a unique, previously unreported, successful outcome for a patient untreated for a tumor affecting a femoral neck considered as painless osteoid osteoma. The lesion was detected by chance at examination for groin injury.
Matovinovic, Damir   +2 more
core   +1 more source

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