Case Reports in Ophthalmology (Jul 2011)

Bilateral Crystalline Corneal Deposits as First Clinical Manifestation of Monoclonal Gammopathy: A Case Report

  • Johannes Steinberg,
  • Mau-Thek Eddy,
  • Toam Katz,
  • Eike Matthiessen,
  • Otto H. Fricke,
  • Gisbert Richard,
  • Stephan J. Linke

DOI
https://doi.org/10.1159/000330334
Journal volume & issue
Vol. 2, no. 2
pp. 222 – 227

Abstract

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Aims: To report the clinical and diagnostic findings of a patient with bilateral corneal deposits caused by an underlying monoclonal gammopathy. Methods: Slit-lamp biomicroscopy, confocal microscopy and additional serological tests were performed on a 35-year-old man presenting with bilateral crystalline corneal deposits. Results: The patient was diagnosed as having monoclonal gammopathy based on elevated levels of serum immunoglobulin G. Confocal microscopy showed highly reflective (protein) deposits throughout the entire cornea, with the highest density in the epithelium and anterior stromal keratocytes. Conclusions: Monoclonal gammopathy, a potential sign of a life-threatening disease, can lead to dense, bilateral corneal deposits. As such changes can occur long before ocular or systemic discomforts appear, an early diagnosis is crucial. Ophthalmologists should be aware of corneal deposits as potential warning signs of monoclonal gammopathy.

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