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Orbital solitary fibrous tumor.
Paganelli, B; Meney, J; Nordmann, J-P; Bennedjaï, A.
Afiliación
  • Paganelli B; Ophthalmology 2, CHNO 15-20, Sorbonne University, 55bis, boulevard du Montparnasse, 75006 Paris, France. Electronic address: bpaganelli0904@gmail.com.
  • Meney J; Ophthalmology 2, CHNO 15-20, Sorbonne University, 55bis, boulevard du Montparnasse, 75006 Paris, France.
  • Nordmann JP; Ophthalmology 2, CHNO 15-20, Sorbonne University, 55bis, boulevard du Montparnasse, 75006 Paris, France.
  • Bennedjaï A; Ophthalmology 2, CHNO 15-20, Sorbonne University, 55bis, boulevard du Montparnasse, 75006 Paris, France.
J Fr Ophtalmol ; 47(9): 104297, 2024 Sep 27.
Article en En | MEDLINE | ID: mdl-39341041
ABSTRACT

INTRODUCTION:

Solitary fibrous tumor (SFT) is a rare borderline mesenchymal tumor typically arising in the pleura and involving the orbit as its most common extra-pleural location. CASE DESCRIPTION We herein describe two cases of orbital SFT arising in both a 69-year-old woman presenting with progressive proptosis of the left eye and a 49-year-old woman presenting with binocular diplopia. The diagnoses relied on histopathological analysis of biopsy samples. Because of the poor local prognosis, we decided to perform an orbital exenteration in the first case. In the second case, a complete resection surgery was performed.

CONCLUSION:

SFT presents classics histological features and immunohistochemical markers that are essential to the diagnosis. SFT is classified as a benign tumor, but in some cases, it can show aggressive behavior with the potential for local tissue invasion and, more scarcely, distant metastasis. This is why complete resection remains the treatment of choice for SFT.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Fr Ophtalmol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Fr Ophtalmol Año: 2024 Tipo del documento: Article