Subconjunctival Myolipoma Confirmed with Immunohistochemical Analysis
Publish place: xxix annual congress of the iranian society of ophthalmology
Publish Year: 1398
نوع سند: مقاله کنفرانسی
زبان: English
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شناسه ملی سند علمی:
ACSOMED29_107
تاریخ نمایه سازی: 30 آذر 1398
Abstract:
Purpose: To describe clinicopathological features of subconjunctival myolipoma Methods: 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).Results: 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. Conclusion: Myolipoma of the soft tissue is an exceedingly rare tumor with less than 50 reported cases in thecurrent 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.
Authors
Fahimeh Asadi-Amoli
Tehran University of Medical Sciences
Mohammad Soleimani
Tehran University of Medical Sciences
Zohreh Nozarian
Tehran University of Medical Sciences
Reza Garebaghi
Tehran University of Medical Sciences
Tooba Ghazanfari
Tehran University of Medical Sciences
Maryam Parvizi
Tehran University of Medical Sciences