Enchondromaof the Skull Base in a Case of Ollier’s Syndrome
محل انتشار: فصلنامه آسیب شناسی ایران، دوره: 10، شماره: 3
سال انتشار: 1394
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 589
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شناسه ملی سند علمی:
JR_IJP-10-3_010
تاریخ نمایه سازی: 13 مرداد 1394
چکیده مقاله:
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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نویسندگان
Shahram Sabeti
Dept. of Pathology, Loghman Hakim Hospital, ShahidBeheshti University of Medical Sciences, Tehran, Iran
Forough Yousefi
Dept. of Pathology, Loghman Hakim Hospital, ShahidBeheshti University of Medical Sciences, Tehran, Iran
Mihan Pourabdollah Toutkaboni
Chronic respiratory DiseasesResearch Center, NRITLD, ShahidBeheshti University of Medical Sciences, Tehran, Iran