Intraconal Orbital Angioleiomyoma: A Case Report and Review of Literature

Message:
Article Type:
Case Report (دارای رتبه معتبر)
Abstract:
Purpose

To present a patient with interaconal orbital angioleiomyoma.

Case Report

A 22-year-old woman presented with painless slowly progressive proptosis. CT and MRI demonstrated a well-defined Interaconal globe size mass (inferomedially). It was isointense in T1 and T2 weighted and homogenously enhanced by Gadolinium. During the surgery, the tumor was excised via a lateral orbitotomy approach; significant hemorrhage and adhesions to surrounding tissues were noticeable. Histopathologic analysis of the specimen revealed smooth muscle cells with vascular components. IHC assay was positive for SMA and CD34, which confirmed the diagnosis of angioleiomyoma. The patient recovered uneventfully and one year of follow-up showed no recurrence or complications.

Conclusion

ALM is an uncommon benign smooth muscle tumor with a vascular component. Orbital involvement (especially interaconal) is extremely rare; caution about considerable intraoperative bleeding and adhesions to surrounding tissue is recommended.

Language:
Persian
Published:
Journal of Ophthalmology Bina, Volume:25 Issue: 2, 2021
Pages:
137 to 141
magiran.com/p2214557  
دانلود و مطالعه متن این مقاله با یکی از روشهای زیر امکان پذیر است:
اشتراک شخصی
با عضویت و پرداخت آنلاین حق اشتراک یک‌ساله به مبلغ 1,390,000ريال می‌توانید 70 عنوان مطلب دانلود کنید!
اشتراک سازمانی
به کتابخانه دانشگاه یا محل کار خود پیشنهاد کنید تا اشتراک سازمانی این پایگاه را برای دسترسی نامحدود همه کاربران به متن مطالب تهیه نمایند!
توجه!
  • حق عضویت دریافتی صرف حمایت از نشریات عضو و نگهداری، تکمیل و توسعه مگیران می‌شود.
  • پرداخت حق اشتراک و دانلود مقالات اجازه بازنشر آن در سایر رسانه‌های چاپی و دیجیتال را به کاربر نمی‌دهد.
In order to view content subscription is required

Personal subscription
Subscribe magiran.com for 70 € euros via PayPal and download 70 articles during a year.
Organization subscription
Please contact us to subscribe your university or library for unlimited access!