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Information Journal Paper

Title

CASE REPORT; ENCHONDROMAOF THE SKULL BASE IN A CASE OF OLLIER’S SYNDROME

Pages

  237-242

Abstract

 Ollier’s syndrome, a variant of multiple ENCHONDROMAtosis, is a rare disease with an estimated prevalence of 1/100,000, characterized by multiple ENCHONDROMAs, asymmetrically involving small bones of the hands and feet, especially the proximal phalanges. INTRACRANIAL ENCHONDROMAs, such as those arising from the SKULL BASE are extremely rare. Herein, we report a 25-year-old female, known case of OLLIER’S DISEASE, presenting with right eyelid ptosis and visual disturbance. Brain MRI revealed a SKULL BASE tumour suspicious to ENCHONDROMA followed by trans-sphenoidal resection. Histologic examination of the excisional biopsy sample confirmed the diagnosis of ENCHONDROMA.

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  • Cite

    APA: Copy

    SABETI, SHAHRAM, YOUSEFI, FOROUGH, & POURABDOLLAH TOUTKABONI, MIHAN. (2015). CASE REPORT; ENCHONDROMAOF THE SKULL BASE IN A CASE OF OLLIER’S SYNDROME. IRANIAN JOURNAL OF PATHOLOGY (IJP), 10(3), 237-242. SID. https://sid.ir/paper/665986/en

    Vancouver: Copy

    SABETI SHAHRAM, YOUSEFI FOROUGH, POURABDOLLAH TOUTKABONI MIHAN. CASE REPORT; ENCHONDROMAOF THE SKULL BASE IN A CASE OF OLLIER’S SYNDROME. IRANIAN JOURNAL OF PATHOLOGY (IJP)[Internet]. 2015;10(3):237-242. Available from: https://sid.ir/paper/665986/en

    IEEE: Copy

    SHAHRAM SABETI, FOROUGH YOUSEFI, and MIHAN POURABDOLLAH TOUTKABONI, “CASE REPORT; ENCHONDROMAOF THE SKULL BASE IN A CASE OF OLLIER’S SYNDROME,” IRANIAN JOURNAL OF PATHOLOGY (IJP), vol. 10, no. 3, pp. 237–242, 2015, [Online]. Available: https://sid.ir/paper/665986/en

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