Abstract
Amyloidosis is a spectrum of disorders characterized by the deposition of amyloid , an extracellular protein in an abnormal fibrillar form, with highly characteristic histopathologic staining properties. Eyelid involvement can be associated with both immunologic (primary) and reactive (secondary) amyloidosis. We present a case of unilateral localized conjunctival and tarsal plate amyloidosis, presenting as ptosis.
Discussion
Localized amyloidosis involving the tarsal conjunctiva and tarsus is a rare cause of chronic eyelid thickening and ptosis.[1] There are various predisposing conditions and systemic involvement can affect various organs. Hence, localized disease warrants a thorough clinical evaluation and laboratory investigation.[2] Absence of any skin changes on the eyelid or symptoms of ocular irritation, in our case, led us to an unsuspecting diagnosis of aponeurotic ptosis. Published literature mention recurrent haemorrhage, ocular irritation, multiple site involvement of conjunctiva, lid thickening and Levator muscle involvement as associated findings with ptosis.[3] Our case had no signs and symptoms other than Ptosis at presentation highlighting the vast spectrum of presentation of amyloidosis .
Source of Funding
No financial support was received for the work within this manuscript.
Conflict of Interest
The authors declare they have no conflict of interest.
References
- Hill V, Brownstein S, Jordan D. Ptosis Secondary to Amyloidosis of the Tarsal Conjunctiva and Tarsus. Am J Ophthalmol. 1997;123(6):852-4. [Google Scholar] [Crossref]
- Kamal S, Goel R, Bodh S. Primary localized amyloidosis presenting as a tarsal mass: Report of two cases. Middle East Afr J Ophthalmol. 2012;19(4):426-8. [Google Scholar] [Crossref]
- Demirci H, Shields C, Eagle R, Shields J. Conjunctival Amyloidosis: Report of Six Cases and Review of the Literature. Surv Ophthalmol. 2006;51(4):419-33. [Google Scholar] [Crossref]