[ Angiosarcome mammaire: A propos d’un cas ]
Volume 20, Issue 2, May 2017, Pages 589–593
I. Rachidi1, Aida Abida2, M.A. Benyahyia3, M. El Yousefi4, and Samir Bargach5
1 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
2 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
3 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
4 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
5 Department of Gynecology-Obstetrics-Oncology and High-Risk Pregnancy, Souissi Maternity Hospital, Ibn Sina University Hospital Center, Rabat, Morocco
Original language: French
Copyright © 2017 ISSR Journals. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Angiosarcoma of the breast is a very rare conjunctive tumor. It is a primitive malignant proliferation of the endothelial cells of the vascular tissue of the gland. It occurs in both a primary form without a known precursor, and a secondary form that has been associated to a history of irradiated breast tissue. Both forms have a malignant behavior and a poor prognosis. We report a case of breast angiosarcoma diagnosed by histology and treatment consisting of a mastectomy supplemented by chemotherapy and radiotherapy.
Author Keywords: cancer, breast, Radiology, Histology, Mastectomy.
Volume 20, Issue 2, May 2017, Pages 589–593
I. Rachidi1, Aida Abida2, M.A. Benyahyia3, M. El Yousefi4, and Samir Bargach5
1 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
2 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
3 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
4 Service de gynécologie obstétrique cancérologie et grossesse à haut risque, Maternité Souissi, Université Mohamed V, Rabat, Morocco
5 Department of Gynecology-Obstetrics-Oncology and High-Risk Pregnancy, Souissi Maternity Hospital, Ibn Sina University Hospital Center, Rabat, Morocco
Original language: French
Copyright © 2017 ISSR Journals. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Angiosarcoma of the breast is a very rare conjunctive tumor. It is a primitive malignant proliferation of the endothelial cells of the vascular tissue of the gland. It occurs in both a primary form without a known precursor, and a secondary form that has been associated to a history of irradiated breast tissue. Both forms have a malignant behavior and a poor prognosis. We report a case of breast angiosarcoma diagnosed by histology and treatment consisting of a mastectomy supplemented by chemotherapy and radiotherapy.
Author Keywords: cancer, breast, Radiology, Histology, Mastectomy.
Abstract: (french)
L'angiosarcome du sein est une tumeur conjonctivale très rare. Il s'agit d'une prolifération maligne primitive des cellules endothéliales du tissu vasculaire de la glande. Présente 2 formes primaire sans précurseur connu, et une forme secondaire après irradiation du sein. Les deux formes ont un comportement malin et un mauvais pronostic. Nous rapportons un cas d'angiosarcome du sein diagnostiqué par l’histologie et le traitement a consisté en une mastectomie complétée par chimiothérapie et radiothérapie.
Author Keywords: cancer, Sein, Radiologie, Histologie, Mastectomie.
How to Cite this Article
I. Rachidi, Aida Abida, M.A. Benyahyia, M. El Yousefi, and Samir Bargach, “Mammary angiosarcoma: About one case,” International Journal of Innovation and Applied Studies, vol. 20, no. 2, pp. 589–593, May 2017.
