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Orbital tumor revealing a systemic sarcoidosis
Samia Hannanachi Sassi1, Rim Dhouib1, Fatma Kanchal1
1Department of Pathology, Salah Azaeiz Institute, Bab Saadoun, 1006 Tunis, Tunisia. fatma.khanchel@gmail.com.
Acta Medica Iranica
|March 22, 2015
Summary
Orbital sarcoidosis, though rare, can mimic orbital tumors in older adults. Early diagnosis and treatment involving systemic corticosteroids are crucial for managing this condition and preventing vision loss.
Area of Science:
- Ophthalmology
- Rheumatology
- Pathology
Background:
- Sarcoidosis commonly affects the eyes, with uveitis being the most frequent manifestation.
- Ocular involvement occurs in about 25% of sarcoidosis patients.
- Orbital sarcoidosis is an uncommon but significant finding.
Observation:
- A 65-year-old woman presented with unilateral eyelid swelling and eye redness.
- Orbital imaging revealed a mass in the inferior right orbital soft tissue.
- Biopsy confirmed nodular, noncaseating granulomas, indicative of sarcoidosis.
Findings:
- The patient exhibited systemic sarcoidosis with hilar and mediastinal lymphadenopathy on CT scan.
- The orbital mass was surgically treated, followed by systemic prednisone.
- The patient showed a positive response to treatment.
Implications:
- Orbital sarcoidosis should be considered in the differential diagnosis of orbital tumors, especially in elderly patients.
- Comprehensive systemic evaluation is essential for diagnosing sarcoidosis.
- Prompt and appropriate therapy, including corticosteroids, can lead to favorable outcomes.
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