Table 1:
Site | Description | Strengths | Limitations | References |
---|---|---|---|---|
AC | Implantation of tumor cells through a corneal defect into the AC | Reliable formation of iris melanomas in an immune-privileged space | Metastases limited and cells can seed extraocular space | In hamsters (16–20) In mice (21–32) In rabbits (33,34–39) |
Suprachoroid | Transcorneal or transconjunctival delivery of cells directly above the choroid | Reliable formation of choroidal melanoma with metastases. Transcorneal approach has minimal extraocular tumor growth. | Deep corneal stromal perforation in transcorneal approach and seeding of cells into the subconjunctival space in transconjunctival approach. | In mice (23,29,40–51) In rabbits (52–60) In rats (61,62) |
Subchoroid | Placement of cells inside an iatrogenic choroidal detachment after retinotomy | Reliable formation of choroidal melanomas within a short period of time | Complex technique with retinotomy. Complications such as vitreous hemorrhage, vitreous cell seeding, retinal detachment, and proliferative vitreoretinopathy. | In hamsters (63) In rabbits (37,64–69) |
Intravitreal | Injection of tumor cells directly into the vitreous through the sclera |
Effective primary tumor growth in the choroid | No extrapulmonary metastases. Changes in the tumor environment. Possible seeding into the anterior chamber. | In mice (70–73) |
AC, anterior chamber.