Results 191 to 200 of about 36,516 (242)
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Chondrosarcoma of the Spine

Spine, 1978
Involvement of the spine by chondrosarcoma is rare. Three recent cases involving the cervical with or without extension to the thoracic spine are reported. Detailed radiologic investigations to evaluate the extent of the disease are essential to management.
M B, Camins   +3 more
openaire   +2 more sources

Mesenchymal chondrosarcoma

International Journal of Oral and Maxillofacial Surgery, 1987
2 cases of this rare tumour in Nigerian subjects is described. Clinical features indicated relatively slow but painful growth, aggravated in 1 case by dental extractions. Radical resection was followed by 6-year survival without recurrence or overt metastasis. Microscopic differential diagnosis is discussed.
H K, Williams   +2 more
openaire   +2 more sources

CHONDROSARCOMA OF THE LARYNX

The Laryngoscope, 1976
Cartilaginous tumors of the larynx are rare, and of those reported, most are chondromas. To date, approximately 157 cartilaginous tumors of the larynx have been reported, but only 37 have been chondrosarcomas. A review of the records of the past 25 years (1948-1974) of the Johns Hopkins University Hospital and the Greater Baltimore Medical Center was ...
R G, Chambers, W, Friedel
openaire   +2 more sources

Pazopanib for treatment of advanced extraskeletal myxoid chondrosarcoma: a multicentre, single-arm, phase 2 trial.

The Lancet Oncology, 2019
BACKGROUND Extraskeletal myxoid chondrosarcoma is a rare sarcoma with low sensitivity to cytotoxic chemotherapy. Retrospective evidence suggests that antiangiogenic drugs could be a treatment option.
S. Stacchiotti   +29 more
semanticscholar   +1 more source

Characterisation of isocitrate dehydrogenase 1/isocitrate dehydrogenase 2 gene mutation and the d‐2‐hydroxyglutarate oncometabolite level in dedifferentiated chondrosarcoma

Histopathology, 2020
Dedifferentiated chondrosarcoma (DDCHS) is an aggressive type of chondrosarcoma that results from high‐grade transformation of a low‐grade chondrosarcoma. Mutations in the isocitrate dehydrogenase (IDH) 1 gene and the IDH2 gene that lead to increased d‐2‐
Nissreen Mohammad   +6 more
semanticscholar   +1 more source

Radiomic analysis of multiparametric magnetic resonance imaging for differentiating skull base chordoma and chondrosarcoma.

European Journal of Radiology, 2019
PURPOSE Patients with skull base chordoma and chondrosarcoma have different prognoses and are not readily differentiated preoperatively on imaging. Multiparametric magnetic resonance imaging (MRI) is a routine diagnostic tool that can noninvasively ...
Longfei Li   +12 more
semanticscholar   +1 more source

Chondrosarcoma of the hand

The Journal of Hand Surgery, 1984
Eighteen consecutive cases with the histologic diagnosis of chondrosarcoma of the hand were reviewed and followed up from 1 to 10 years. The primary tumor originated without a preexisting lesion in 78%. Secondary tumors arose in patients who had multiple enchondromas but not in patients with a solitary enchondroma. The onset is usually in the 60- to 80-
openaire   +2 more sources

Enchondroma and Chondrosarcoma

Seminars in Musculoskeletal Radiology, 2000
Enchondroma and chondrosarcoma are two of the most commonly encountered primary bone lesions in the typical radiology practice. The purpose of this article is to review the clinical, radiological, and pathological features that distinguish conventional chondrosarcoma from enchondroma.
D J, Flemming, M D, Murphey
openaire   +2 more sources

How to Diagnose Enchondroma, Bone Infarct, and Chondrosarcoma.

Current problems in diagnostic radiology, 2019
Enchondromas are among the most common benign tumors seen in the skeleton. They are encountered frequently in routine clinical practice. The purpose of this review is to help radiologists confidently diagnose enchondroma and distinguish it from other ...
M. Mulligan
semanticscholar   +1 more source

Chondrosarcoma of the Pelvis

Clinical Orthopaedics and Related Research, 1997
Thirty-one patients with chondrosarcoma of the pelvis were reviewed. The median followup period of the surviving patients was 66 months. Thirteen of 23 tumors after surgery with inadequate margins (57%) and 1 of 8 after surgery with adequate margins (13%) relapsed locally.
T, Ozaki   +4 more
openaire   +2 more sources

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