Vision Pan-America (Mar 2012)

Melkersson-Rosenthal Syndrome: A forgotten diagnosis

  • Michael D. Karon,
  • Alejandra A. Valenzuela

DOI
https://doi.org/10.15324/vpa.v11i1.4
Journal volume & issue
Vol. 11, no. 1
pp. 21 – 22

Abstract

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The rare, non-caseating, granulomatous disease known as Melkersson-Rosenthal syndrome (MRS) can be diagnostically difficult especially when not presenting as the characteristic triad of facial palsy, facial edema, and fissured tongue.1 We present a case of a 65-year-old female with a 15-year history of recurrent bilateral upper eyelid swelling previously unsuccessfully treated for a presumed lid allergy and rosacea. Following imaging and histopathology results, she has now been diagnosed with Melkersson-Rosenthal syndrome. Since this disease is typically refractory to treatment, she is being followed and treated with cosmetic eyelid skin reduction if necessary during inactive stages of the disease.

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