ABSTRACT Amyloidosis is characterized by the extracellular deposition of amyloid protein fibrils in tissues, including the conjunctiva, due to their insolubility in proteolytic enzymes. Conjunctival amyloidosis, particularly involving the eyelid conjunctiva, is a rare clinical entity. We report the case of a 60-year-old Caucasian female who presented with a unilateral lesion in the inferior bulbar conjunctiva, extending to the entire inferior tarsal region and fornix. The lesion appeared as an extensive, elevated, pinkish-yellowish nodular mass with poorly defined borders. An […]

ABSTRACT Amyloidosis is a rare disease in which ocular involvement may occur as an isolated event or associated with a systemic disease. This paper describes two clinical cases of ophthalmologic manifestations of amyloidosis: a bilateral eyelid lesion similar to xanthelasma and tarsal conjunctival disease similar to follicular conjunctivitis. The anatomopathological analysis confirmed the diagnosis.

ABSTRACT Amyloidosis is characterized by extracellular deposition of protein amyloid fibrils in tissues, including conjunctiva, which are insoluble in proteolytic proteins. Conjunctival amyloidosis specifically in the palpebral conjunctiva is a rare finding in clinical practice. The authors described the case of a 71-year-old caucasian male patient, with bilateral lesions located in the lower eyelid conjunctiva, elevated, well-defined, yellowish, combined with destabilized eyelids. Surgical excision of the lesions was performed, and the histological examination confirmed conjunctival amyloidosis. There was no recurrence […]