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Intraocular lacrimal gland choristoma involving iris and ciliary body

J A Shields1, R N Hogan, C L Shields

  • 1Oncology Service, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

American Journal of Ophthalmology
|June 14, 2000
PubMed

Insights

This case report details an intraocular lacrimal gland choristoma in a 12-month-old male. The study highlights unique clinical features aiding in the diagnosis of this rare iris mass.

Area of Science:

  • Ophthalmology
  • Pathology
  • Histopathology

Background:

  • Lacrimal gland choristomas are rare congenital tumors.
  • Diagnosis often relies on characteristic clinical and histopathological findings.

Observation:

  • A 12-month-old male presented with a large iris mass present since birth.
  • Clinical examination suggested a lacrimal gland choristoma.
  • Ultrasound biomicroscopy and histopathology were utilized for diagnosis.

Findings:

  • The iris mass was surgically removed via iridocyclectomy.
  • Histopathological examination confirmed the diagnosis of lacrimal gland choristoma.
  • The lesion exhibited unique clinical features.

Implications:

  • Recognition of unique clinical features can aid in the early diagnosis of intraocular lacrimal gland choristoma.
  • This case contributes to understanding the clinical presentation and diagnosis of this rare condition.
Abstract

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