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Management of corneal opacification associated with epibulbar choristomata
  1. RICHARD NEWSOM
  1. Sussex Eye Hospital, Brighton
  2. Croydon Eye Unit, Mayday Hospital
  3. Royal Sussex County Hospital, Brighton
  4. Sussex Eye Hospital, Brighton
  1. WILLIAM AYLIFFE,
  2. SUSHMA DHAR-MUNSHI
  1. Sussex Eye Hospital, Brighton
  2. Croydon Eye Unit, Mayday Hospital
  3. Royal Sussex County Hospital, Brighton
  4. Sussex Eye Hospital, Brighton
  1. NIGEL KIRKHAM
  1. Sussex Eye Hospital, Brighton
  2. Croydon Eye Unit, Mayday Hospital
  3. Royal Sussex County Hospital, Brighton
  4. Sussex Eye Hospital, Brighton
  1. CHRISTOPHER LIU
  1. Sussex Eye Hospital, Brighton
  2. Croydon Eye Unit, Mayday Hospital
  3. Royal Sussex County Hospital, Brighton
  4. Sussex Eye Hospital, Brighton
  1. Mr C Liu, Sussex Eye Hospital, Eastern Road, Brighton BN2 5BF

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Editor,—Choristomas are the commonest limbal tumours in children.1 Four types are recognised—dermoid, dermolipoma, single tissue, and complex choristoma. They arise from metaplastic transformation in the mesoblast lying between the optic nerve and the surface ectoderm. Epithelial and dermal, neural, cartilagenous, smooth muscle, lacrimal, sweat, or sebaceous gland tissue may be present.2-4 They are well circumscribed, white or pale yellow, and may be single or multiple, unilateral, or bilateral5 or form a ring.3 Occasionally, epibulbar choristomata are associated with superficial corneal involvement characterised by a vascularised pannus particularly in those containing lacrimal tissue.6

CASE 1

A 7 year old Malaysian Chinese boy was referred to one of us (CL) with cloudy corneas since birth. His vision had always been poor but no strabismus developed. The pregnancy and developmental history were otherwise normal. There was no family history of ocular disease.

Examination revealed 6/18 part vision right …

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