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Progressive Hemifacial Atrophy With Contralateral Uveitis: A Case Report.

Onder Ayyildiz1, Simel Ayyildiz2, Ali Hakan Durukan1

  • 1Department of Ophthalmology, Gulhane Military Medical Academy, Ankara, Turkey.

Iranian Red Crescent Medical Journal
|October 17, 2015
PubMed
Summary

Parry-Romberg syndrome (PRS) involves facial tissue atrophy and common ophthalmic issues. Steroid therapy effectively treated a patient with PRS who developed granulomatous uveitis and retinal vasculitis.

Keywords:
Parry Romberg SyndromeProgressive Hemifacial AtrophyUveitis

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Area of Science:

  • Ophthalmology
  • Dermatology
  • Genetics

Background:

  • Parry-Romberg syndrome (PRS) is a rare disorder characterized by progressive atrophy of facial tissues.
  • Ophthalmic complications are frequently observed in PRS patients, including uveitis and retinal vasculitis.

Observation:

  • A patient with right-sided PRS presented with left-sided granulomatous uveitis and peripheral retinal vasculitis.
  • The patient's condition was managed with topical and systemic corticosteroid therapy.

Findings:

  • Corticosteroid treatment led to significant regression of the uveitic reaction within three months.
  • This case highlights the potential for PRS to manifest with complex ocular inflammatory conditions.

Implications:

  • A multidisciplinary approach is crucial for managing the diverse manifestations of PRS.
  • Prompt and appropriate treatment, including immunosuppression, can effectively manage ocular complications in PRS.