[A severe unilateral corneal ectasia in children]

J Fr Ophtalmol. 2023 Dec;46(10):1244-1246. doi: 10.1016/j.jfo.2023.05.033. Epub 2023 Nov 17.
[Article in French]

Abstract

Purpose: We report a case of unilateral Terrien's marginal degeneration in a 14-year-old girl.

Clinical case: Slit-lamp examination of the affected eye revealed 360° circumferential lipid deposits with 6mm of superior limbal distension, superficial neovascularization, a zone of corneal thinning from 3:00 to 9:00 with a zone of corneomalacia at 11:00. The remainder of the cornea was clear, without fluorescein staining or anterior chamber reaction.

Discussion: Terrien's marginal degeneration (TMD) is typically known to occur bilaterally in men over the age of 40. Terrien's degeneration must be differentiated from other causes of peripheral corneal thinning; the primary differential diagnosis is Fuchs' marginal keratitis. Other causes of corneal thinning must be ruled out, including Mooren's ulcer. In Terrien's degeneration, there is no central mined edge in the thinning sulcus, the epithelium remains intact, and affected patients do not present with pain. Other differential diagnoses include pellucid marginal degeneration and sulcus degeneration, which are characterized by the absence of lipid infiltrates associated with the central region of the thinning zone, thus distinguishing them from TMD.

Conclusion: It is important to keep in mind that Terrien's marginal degeneration can occur in children.

Keywords: Cornea; Corneal transplantation; Cornée; Dystrophie de Terrien; Greffe de cornée; Pediatric; Pédiatrie; Terrien's marginal degeneration.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Adolescent
  • Child
  • Cornea
  • Corneal Diseases* / complications
  • Corneal Diseases* / diagnosis
  • Corneal Dystrophies, Hereditary* / diagnosis
  • Corneal Ulcer* / complications
  • Dilatation, Pathologic / complications
  • Dilatation, Pathologic / diagnosis
  • Female
  • Humans
  • Lipids
  • Male

Substances

  • Lipids