Search

Your search keyword '"ZINEB ALAMI"' showing total 2 results
Start Over Author "ZINEB ALAMI" Topic malignant tumour
2 results on '"ZINEB ALAMI"'

1. Paravertebral extraskeletal myxoid chondrosarcoma: a case report and review of the literature

Author

Fatima Zahra Farhane, Zineb Alami, Touria Bouhafa, Abderrahmane Elmazghi, and Khalid Hassouni

Subjects
extraskleletal myxoid chondrosarcoma, paravertebral, malignant tumour, Medicine
Abstract

The extraskeletal myxoid chondrosarcoma (CME) is a rare malignant soft tissue tumour described as a distinct clinical, histological, immunohistochemical, genetical and evolutive entity. It represents only 2.5% of soft tissue sarcomas. Its individualization is important because it has a long and indolent clinical course, and tumour-related death often occurs after a long survival period. The diagnostic key is morphological supported by immunohistochemistry and genetics t (9; 22) that allow differentiating it from other tumours with myxoid stroma and from chordoma. This report describes a patient with paravertebral extraskeletal myxoid chondrosrcoma with a high locoregional extension.

Published
2015
Full Text
View/download PDF

2. Paravertebral extraskeletal myxoid chondrosarcoma: a case report and review of the literature

Author

Touria Bouhafa, Zineb Alami, Khalid Hassouni, Abderrahmane Elmazghi, and Fatima Zahra Farhane

Subjects
Adult, Pathology, medicine.medical_specialty, Survival period, Chondrosarcoma, Myxoid stroma, Case Report, Diagnosis, Differential, medicine, Humans, malignant tumour, lcsh:R5-920, Extraskleletal myxoid chondrosarcoma, paravertebral, business.industry, lcsh:Public aspects of medicine, Extraskleletal myxoid chondrosarcoma, paravertebral, malignant tumour, Soft tissue, lcsh:RA1-1270, General Medicine, Extraskeletal Myxoid Chondrosarcoma, medicine.disease, Immunohistochemistry, Female, Chordoma, Differential diagnosis, lcsh:Medicine (General), business, Neoplasms, Connective and Soft Tissue
Abstract

The extraskeletal myxoid chondrosarcoma (CME) is a rare malignant soft tissue tumour described as a distinct clinical, histological, immunohistochemical, genetical and evolutive entity. It represents only 2.5% of soft tissue sarcomas. Its individualization is important because it has a long and indolent clinical course, and tumour-related death often occurs after a long survival period. The diagnostic key is morphological supported by immunohistochemistry and genetics t (9; 22) that allow differentiating it from other tumours with myxoid stroma and from chordoma. This report describes a patient with paravertebral extraskeletal myxoid chondrosrcoma with a high locoregional extension.

Published
2015

Catalog

Books, media, physical & digital resources
See catalog results