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Sclerokeratitis and facial skin lesions: a case report of pyoderma gangrenosum and its response to dapsone therapy.

AbstractPURPOSE:
This documents the evaluation and management of a patient with an unusual destructive external ocular disorder in the context of progressively disfiguring dermatitis.
METHODS:
Observational case report including ophthalmologic examination with conjunctival and corneal scraping, radiologic studies of the sinuses and chest, skin, conjunctival, and scleral biopsies, and serologic studies.
RESULTS:
Biopsies, cultures, and serologic testing led to the conclusion that the patient had pyoderma gangrenosum. Therapy with dapsone resulted in preservation of vision and resolution of the oculocutaneous inflammation.
CONCLUSIONS:
Pyoderma gangrenosum is a rare autoimmune disorder that can affect the eye. Biopsy of affected tissue is the key to diagnosis. Immunomodulating therapy can be a useful adjunct to the traditional steroid therapy.
AuthorsLaura A Teasley, C Stephen Foster, Stefanos Baltatzis
JournalCornea (Cornea) Vol. 26 Issue 2 Pg. 215-9 (Feb 2007) ISSN: 0277-3740 [Print] United States
PMID17251816 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Dapsone
Topics
  • Adult
  • Anti-Inflammatory Agents, Non-Steroidal (therapeutic use)
  • Biopsy
  • Dapsone (therapeutic use)
  • Face
  • Female
  • Follow-Up Studies
  • Humans
  • Keratitis (drug therapy, etiology, pathology)
  • Pyoderma Gangrenosum (complications, drug therapy, pathology)
  • Scleritis (drug therapy, etiology, pathology)
  • Severity of Illness Index

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