AI Article Synopsis

  • Amyloidosis involves abnormal protein deposits in tissues, leading to various clinical presentations, from localized issues to widespread systemic disease.
  • Ocular amyloidosis can manifest as localized conjunctival conditions, which are usually not linked to systemic diseases, and might sometimes be associated with immunologic disorders.
  • A case report highlights a patient with bilateral conjunctival amyloidosis, diagnosed through biopsy after initial concerns of a malignant lesion, emphasizing the need for proper histopathologic evaluation to confirm such rare conditions.

Article Abstract

Amyloidosis is a group of disorders characterized by deposition of an extracellular protein, known as amyloid, in an abnormal fibrillar form with highly characteristic histopathologic staining properties. The clinical presentation can vary from a focal, localized lesion where amyloidosis has minor clinical consequences to extensive systemic disease that can involve any organ system of the body. Ocular amyloidosis can occur as a localized lesion or as a part of a systemic disorder. Conjunctival amyloidosis is an uncommon condition that is rarely associated with systemic disease. It may be a manifestation of an immunologic disorder. We report the case of a patient with bilateral conjunctival amyloidosis who was referred to us with the suspicion of a malignant conjunctival lesion. Examination of both eyes showed a yellow-pink mass with prominent intrinsic vessels, subconjunctival hemorrhage, and ectropion of the left lower eyelid. Diagnosis of primary localized conjunctival amyloidosis was made based on histopathologic evaluation of incisional biopsy and negative systemic work-up. Ocular amyloidosis is a rare disease that is slowly progressive and has a wide variety of clinical presentations. Consequently, the clinical diagnosis is often overlooked or delayed. Definitive diagnosis is achieved through histopathologic evaluation of biopsy specimen.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5126439PMC
http://dx.doi.org/10.1155/2016/5610753DOI Listing

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