Journal of the Korean Ophthalmological Society 2004;45(9):1567-1572.
Published online September 1, 2004.
Primary Localized Amyloidosis of the Lacrimal Gland.
Hyuk Jin Choi, Ho Kyung Choung, Sang In Khwarg
1Department of Ophthalmology, Seoul National University College of Medicine, Seoul, Korea.
2Department of Ophthalmology, Seoul National University Boramae Hospital, Seoul, Korea. hokyung@brm.co.kr
3Seoul Artificial Eye Center, Seoul National University Hospital Clinical Research Institute, Seoul, Korea.
눈물샘에 발생한 일차성 국소성 아밀로이드증 1예
최혁진 ( Hyuk Jin Choi ) , 정호경 ( Ho Kyung Choung ) , 곽상인 ( Sang In Khwarg )
Abstract
PURPOSE
Amyloidosis involving the lacrimal gland is a very rare condition. We report our experience with a case of primary localized amyloidosis of the lacrimal gland. METHODS: A 36-year-old woman presented with a palpable mass on the right temporal upper eyelid of 1-month duration. The non-tender, firm, and movable mass was palpable on the area of the right lacrimal gland. There were no abnormalities on slit-lamp biomicroscopic and fundus examinations, nor was proptosis or limitation of extraocular movement seen. Excisional biopsy through Krnlein operation and histopathologic examination were followed by orbital computerized tomography (CT). RESULTS: CT scan revealed a homogeneous soft tissue mass containing focal calcification in the right lacrimal gland. Hematoxylin and eosin stained sections showed pink amorphous hyaline deposits and Congo red-stained sections demonstrated dichroism and birefringence under polarized light microscopy, consistent with the diagnosis of amyloidosis. In an additional study, no systemic involvement was noted. CONCLUSIONS: In any case presenting temporal upper eyelid swelling and homogeneous mass containing focal calcification involving the lacrimal gland on CT scan, amyloidosis should be differentiated and it is necessary to confirm the diagnosis through biopsy and systemic work-up.
Key Words: Lacrimal gland;Primary localized amyloidosis


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