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International Journal of Innovation and Applied Studies
ISSN: 2028-9324     CODEN: IJIABO     OCLC Number: 828807274     ZDB-ID: 2703985-7
 
 
Saturday 26 November 2022

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Malignant solitary fibrous tumor: A case report


[ Tumeur fibreuse solitaire maligne: A propos d’un cas ]

Volume 34, Issue 2, November 2021, Pages 136–140

 Malignant solitary fibrous tumor: A case report

Karima Idrissi Serhrouchni1, I. Elihiai2, M. Eljiar3, Jinane Kharmoum4, and Mariame Chraibi5

1 Department of Pathology, University Hospital of Tangier, Faculty of Medecine, Abdelmalek Essaadi University, Tangier, Morocco
2 Service d’Anatomie Pathologique, Centre Hospitalier Universitaire de Tanger, Faculté de Médecine de Tanger, Université Abdelmalek Essadi, Morocco
3 Service d’Anatomie Pathologique, Centre Hospitalier Universitaire de Tanger, Faculté de Médecine de Tanger, Université Abdelmalek Essadi, Morocco
4 Department of Pathology, University Hospital of Tangier, Faculty of Medecine, Abdelmalek Essaadi University, Tangier, Morocco
5 Department of Pathology, University Hospital of Tangier, Faculty of Medecine, Abdelmalek Essaadi University, Tangier, Morocco

Original language: French

Copyright © 2021 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


Solitary fibrous tumor is a rare mesenchymal tumor. It located preferentially at pleural, rarely seen in extrathoracic sides. This tumor shows a high risk of local recurrence and a poor prognosis within an incomplete resection. The authors present a case of malignant solitary fibrous tumor in a 39-year-old woman, diagnosed at the antero-medial part of the left thigh. In trying to recall the clinical and pathological features and treatment of this rare entity.

Author Keywords: Solitary fibrous tumor, mesenchyme, malignant, soft tissue.


Abstract: (french)


La tumeur fibreuse solitaire est une tumeur rare du mésenchyme. Elle se développe préférentiellement au niveau pleural, rarement en extrathoracique. C’est une tumeur qui présente un risque élevé de récidives locales et dont le pronostic dépend de la qualité d’exérèse. Les auteurs présentent un cas d’une tumeur fibreuse solitaire maligne chez une patiente de 39 ans, diagnostiquée au niveau de la partie antéro-interne de la cuisse gauche. En essayons de rappeler des caractéristiques cliniques, pathologiques et thérapeutique de cette rare entité.

Author Keywords: Tumeur fibreuse solitaire, mésenchyme, malin, parties molles.


How to Cite this Article


Karima Idrissi Serhrouchni, I. Elihiai, M. Eljiar, Jinane Kharmoum, and Mariame Chraibi, “Malignant solitary fibrous tumor: A case report,” International Journal of Innovation and Applied Studies, vol. 34, no. 2, pp. 136–140, November 2021.