AN EXTREMELY RARE ORBITAL TUMOR

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SALOUR S.H.; REZAEE KANAVI M.; KARIMI S.

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Journal: BINA Year:2011 | Volume:16 | Issue:2 (63) Page(s): 169-172

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Information Journal Paper

Title

AN EXTREMELY RARE ORBITAL TUMOR

Author(s)

SALOUR S.H. | REZAEE KANAVI M. | KARIMI S. | Issue Writer Certificate

Keywords

ORBITA TUMORQ3

GRANULAR CELL TUMORQ3

Abstract

Purpose: To present a case of orbital GRANULAR CELL TUMOR, a rare orbital tumor. Case Report: A 55-year-old woman presented with binocular diplopia and right ocular displacement. The problem had initiated 3 years ago. A firm nontender mass at the region of the right lower lid was visible. Orbital CT-scan disclosed a well-defined mass in the inferior right orbit with involvement of the inferior muscles. Subtotal excision of the mass, and histopathological and immunohistochemical studies revealed GRANULAR CELL TUMOR. Postoperatively, there was improvement in patient's signs and symptoms. Because of residual tumor, she was referred for radiotherapy. Conclusion: Immunohistochemical and histopathological studies are beneficial in diagnosis of rare orbital tumors.

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APA: Copy

SALOUR, S.H., REZAEE KANAVI, M., & KARIMI, S.. (2011). AN EXTREMELY RARE ORBITAL TUMOR. BINA, 16(2 (63)), 169-172. SID. https://sid.ir/paper/42531/en

Vancouver: Copy

SALOUR S.H., REZAEE KANAVI M., KARIMI S.. AN EXTREMELY RARE ORBITAL TUMOR. BINA[Internet]. 2011;16(2 (63)):169-172. Available from: https://sid.ir/paper/42531/en

IEEE: Copy

S.H. SALOUR, M. REZAEE KANAVI, and S. KARIMI, “AN EXTREMELY RARE ORBITAL TUMOR,” BINA, vol. 16, no. 2 (63), pp. 169–172, 2011, [Online]. Available: https://sid.ir/paper/42531/en

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