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       XXIX Annual Congress of the Iranian Society of Ophthalmology        بـیــست و نهمین کنــگــره سـالیـانه انـجـمـن چـشـم پـزشـکی ایـــران
مقاله Abstract

Title: Subconjunctival Myolipoma Confirmed with Immunohistochemical Analysis
Author(s): Fahimeh Asadi-Amoli 1 , Mohammad Soleimani 2, Zohreh Nozarian 1, Reza Garebaghi 3, Tooba Ghazanfari 4, Maryam Parvizi 4, Keivan Rezaei 2 , Seyed Ali Tabatabaei 2
Presentation Type: Oral
Subject: Cornea and Anterior Segment
Presenting Author:
Name: Mohammad Soleimani
Affiliation :(optional) Tehran University of Medical Sciences
E mail:
Mobile: 09121096496

To describe clinicopathological features of subconjunctival myolipoma


A 17-year-old female presented with a white-pink mass in the left upper bulbar conjunctiva. The lesion extended and finished in the forniceal conjunctiva. The patient revealed normal complete ocular examinations and underwent complete surgical excision of the mass due to cosmetic concerns. The tumor was examined with light–microscopy, following Hematoxylin and Eosin (H&E), Masson-trichrome, and Immunohistochemical (IHC) staining using the following antibodies: HMB45, actin, desmin, Estrogen Receptor (ER), S 100 protein as well as Smooth Muscle Actin (SMA).


A definite diagnosis of subconjunctival myolipoma was obtained following a detailed pathological assessment. Six months postoperatively, no tumor recurrence was noted, and ocular examinations were within normal limits.


Myolipoma of the soft tissue is an exceedingly rare tumor with less than 50 reported cases in the current literature and has female preponderance, and is commonly reported in the abdominal cavity and retroperitoneum. However, to date, only two cases of orbital myolipoma have been reported in the literature. The current report is the first case of subconjunctival myolipoma.


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