J Korean Ophthalmol Soc.  2010 Aug;51(8):1142-1145.

A Case of an Orbital Myxoma

Affiliations
  • 1Department of Ophthalmology, Pusan National University School of Medicine, Busan, Korea. hychoi@pusan.ac.kr

Abstract

PURPOSE
Orbital myxoma is an extremely rare tumor. To date, only a few cases have been reported in the literature. The present study reports a case of an orbital myxoma and demonstrates the clinical and histological features.
CASE SUMMARY
A 37-year-old woman presented with a painless movable mass in the orbital margin of the left eye. Computed tomography of the orbit revealed a sharply outlined solid mass, and an excisional biopsy was performed. The excised specimen consisted of a 17x9x10 mm3 brownish mass of scattered spindle cells and small vascular spaces in a fibromyxoid background. Immunohistochemically, the tumor cells were not immunoreactive for SMA, S-100 protein or CD34. Histopathologic examination revealed the tumor to be a myxoma. There was no mass lesion in computed tomography of the orbit, and no recurrence or complications were found one month after removal.
CONCLUSIONS
When a patient presents with a painless and movable mass in the orbital area, orbital myxoma should be considered as a possible diagnosis. The orbital myxoma with bone invasion should be completely removed to prevent the lesion from recurring.

Keyword

Orbital myxoma

MeSH Terms

Adult
Biopsy
Eye
Female
Humans
Myxoma
Orbit
Recurrence
S100 Proteins
S100 Proteins

Figure

  • Figure 1. Preoperative and postoperative CT findings of the myxoma. There is sharply outlined solid mass with abutment of the left inferior orbital rim.

  • Figure 2. Surgically excised specimen consisted of a 17×9×10 mm3 solid and brownish mass.

  • Figure 3. Scattered spindle cells and small vascular spaces in a fibromyxoid background (H&E; (A) ×100, (B) ×400).


Reference

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