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Updated: Aug 13, 2026

Induction of Ocular Surface Inflammation and Collection of Involved Tissues
Published on: August 4, 2022
[Intracorneal granulomatous inflammation]
W Meyer-Riemann1, C D Quentin, M Vogel
1Universitäts-Augenklinik, Robert-Koch-Strasse 40, 37075 Göttingen.
A rare corneal granuloma developed months after phototherapeutic keratectomy (PTK) in a patient with lattice corneal dystrophy. Histology revealed inflammatory cells, but a link to PTK was deemed unlikely.
Area of Science:
- Ophthalmology
- Corneal Surgery
- Pathology
Background:
- Lattice corneal dystrophy is a hereditary condition affecting the cornea.
- Phototherapeutic keratectomy (PTK) is a surgical procedure used to treat corneal irregularities.
Observation:
- A 33-year-old man with lattice corneal dystrophy developed an intracorneal tumor 8 months after PTK.
- No history of foreign body injury or clear cause for the tumor was identified.
Findings:
- Histological examination of the excised tumor revealed a dense inflammatory infiltrate.
- The infiltrate included epithelioid cells, histiocytes, lymphocytes, eosinophilic leukocytes, and Touton giant cells.
- No signs of generalized granulomatous inflammation were present.
Implications:
- This case presents a rare monosymptomatic intracorneal granulomatous infiltration.
- The granuloma's occurrence months after PTK, without a clear link, is unusual.
- Potential diagnoses include xanthogranuloma or sarcoidosis, though a pathogenetic connection to PTK is unlikely.
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