A, Slitlamp examination before topical rebamipide treatment shows a pinkish tumor located in the nasal bulbar conjunctiva with abnormal vessels. B, Indocyanine green angiography of the anterior segment before topical rebamipide treatment displays a markedly stained lesion corresponding to the tumor. Abnormal dilated vessels associated with the tumor extend to the cornea (arrowheads). C, Slitlamp examination 3 months after starting topical rebamipide treatment demonstrates mild hyperemia without tumor formation in the left eye. D, Indocyanine green angiography 3 months after starting topical rebamipide treatment shows no staining in the conjunctiva.
A, Before rebamipide treatment, the initial lesion shows acanthosis with mild nuclear atypia (asterisk) as well as conjunctival dysplasia. Noncancerous epithelium is noted in the surgical margin (arrowhead) (hematoxylin-eosin, original magnification ×200). B, Goblet cells (arrowheads) are hardly noted in the adjacent normal conjunctiva (2/high-power field) before rebamipide treatment (hematoxylin-eosin, original magnification ×400). C, After topical rebamipide treatment, the conjunctival epithelium shows a smooth surface with an increased number of goblet cells (25/high-power field) (hematoxylin-eosin, original magnification ×400).
Kase S, Shinohara T, Kase M. Effect of Topical Rebamipide on Human Conjunctival Goblet Cells. JAMA Ophthalmol. 2014;132(8):1021-1022. doi:10.1001/jamaophthalmol.2014.431
The conjunctival epithelium contains mucin-secreting goblet cells, which are essential for maintenance of a healthy ocular surface.1 It has been demonstrated that topical administration of rebamipide, an antiulcer agent, increases the mucin level of the tear film and improves the ocular surface in dry eye syndrome.2 Indeed, rebamipide increased the number of goblet cells in rabbit and murine conjunctivas in vivo.3,4 Ríos et al demonstrated that rebamipide led to proliferation of cultured rat conjunctival goblet cells,5 subsequently stimulating secretion from the cells.6 However, there has been no evidence that rebamipide exerts a strong action on human goblet cell behavior. This is the first report, to our knowledge, showing markedly increased goblet cells after administration of topical rebamipide in a patient with conjunctival dysplasia.
A man in his late 70s had conjunctival hyperemia in the left eye. He was referred to our hospital because a conjunctival tumor was initially observed at a clinic. His visual acuity was 20/25 OS and his intraocular pressure was normal. Slitlamp examination revealed a pinkish tumor located in the nasal bulbar conjunctiva (Figure 1A). Indocyanine green angiography of the anterior segment demonstrated a markedly stained lesion corresponding to the tumor (Figure 1B). Dilated vessels associated with the tumor extended to the cornea (Figure 1B). The right eye was healthy. Because carcinoma in situ was initially suspected, the conjunctival tumor and the associated corneal epithelial lesion were excised with a 3-mm surgical margin after obtaining written informed consent. The conjunctival deficit was completely reconstructed using a rotation flap. Histologically, the conjunctival tumor showed mild dysplasia (Figure 2A). The lesion of the dysplasia was located at the site 2 mm nasal to the corneal limbus. The adjacent noncancerous conjunctiva contained a few goblet cells (2/high-power field) (Figure 2B). Surgical margins were free of dysplasia cells. The patient used topical rebamipide eyedrops 4 times a day for 3 months without other topical agents to support healing of the postoperative corneal erosion. Slitlamp examination demonstrated smooth bulbar conjunctiva of the left eye (Figure 1C) 3 months after starting treatment with rebamipide. Indocyanine green angiography showed no staining or dilated vessels in the conjunctiva (Figure 1D). After oral informed consent was obtained, a biopsy was performed at the bulbar conjunctiva 2 mm nasal to the corneal limbus to evaluate how the epithelial atypia changed. Histologically, the conjunctival epithelium contained an increased number of goblet cells (25/high-power field) without cellular atypia (Figure 2C). After 6 months’ follow-up, the patient is well without recurrence of the tumor.
Rebamipide is considered to increase the number of goblet cells of the tissues in rabbit and mouse models.3,4 For the first time, to our knowledge, our study has demonstrated that use of rebamipide alone for 3 months resulted in a markedly increased number of goblet cells in the conjunctival epithelium of a human. The results also verify in vitro evidence that rebamipide led to an increased number of goblet cells of the rat conjunctiva.5,6
A limitation of this study is its short follow-up time. A previous article demonstrated that topical rebamipide could be safely used for 4 weeks in patients with dry eye syndrome and that its effectiveness would last for at least 2 weeks after the end of treatment.2 Careful observation is mandatory to ensure the safety of topical rebamipide. Also, the conjunctiva of the fellow eye was not available in this study. Further studies are needed to verify the goblet cells in the conjunctival tissues of human eyes that have not undergone surgery.
Corresponding Author: Satoru Kase, MD, Department of Ophthalmology, Teine Keijinkai Hospital, Maeda 1-12, Teine-ku, Sapporo 006-0811, Japan (email@example.com).
Author Contributions: Dr S. Kase had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Study concept and design: S. Kase, M. Kase.
Acquisition, analysis, or interpretation of data: Shinohara.
Drafting of the manuscript: S. Kase.
Critical revision of the manuscript for important intellectual content: Shinohara, M. Kase.
Statistical analysis: S. Kase.
Obtained funding: S. Kase, Shinohara.
Administrative, technical, or material support: S. Kase.
Study supervision: Shinohara, M. Kase.
Conflict of Interest Disclosures: None reported.