# Two distinctly located primary orbital melanomas following evisceration for congenital corneal staphyloma: a case report and brief literature review

**Authors:** Chaona Zhou, Pengsen Wu, Fangwei Ying, Jing Rao, Yanlin Wen, Guiqin Liu

PMC · DOI: 10.3389/fmed.2025.1662161 · Frontiers in Medicine · 2026-01-05

## TL;DR

A 14-year-old girl developed two orbital melanomas nine years after an eye procedure for a congenital eye condition, suggesting a possible link between pigmented nevi and tumor formation.

## Contribution

The paper presents a rare case of two primary orbital melanomas following evisceration and discusses potential risk factors like blue nevi and surgical choices.

## Key findings

- Two distinct primary orbital melanomas were identified nine years after evisceration and implantation of a MEDPOR® prosthesis.
- Histopathology confirmed malignant melanoma with specific marker positivity (S-100, Melan-A, HMB-45) and no pathogenic variants detected via NGS.
- Blue nevi may be an underrecognized risk factor for orbital melanoma, suggesting enucleation could be preferable to evisceration in certain cases.

## Abstract

To report an unusual case of two distinct primary orbital melanomas emerged 9 years following evisceration for congenital corneal staphyloma and implantation of a MEDPOR® prosthesis.

A 14-year-old female with congenital blindness and progressive right globe enlargement since birth, accompanied by multiple cutaneous blue nevi, initially underwent right eye evisceration with MEDPOR® implant placement in 2012, revealing congenital corneal staphyloma and proliferative vitreoretinopathy on histopathology. Nine years later, she presented with chronic right eye tearing and intermittent bloody discharge. Examination revealed a prominent scalp blue nevus with satellite lesions, mild orbital implant protrusion, conjunctival congestion, and a subconjunctival black mass. MRI identified a 1.9 cm T1-slight hyperintense, T2-hypointense mass superior to the implant, with inferior rectus thickening. Surgical excision yielded two masses: a 41 mm inferonasal lesion (partially pigmented, unencapsulated) and a 20 mm superior–posterior black, spherical mass. Histopathology confirmed orbital malignant melanoma, with tumor cells positive for S-100 (3+), Melan-A (3+), and HMB-45 (2+). NGS revealed no pathogenic variants, and PET/CT showed no metastasis. She subsequently underwent postoperative radiotherapy and maintains good overall health until June 2025.

This article reports a case of primary orbital melanoma presenting as two tumors within a single orbit following evisceration, with a focus on elucidating the origin of tumor cells and their relationship with pigmented nevi and orbital implants.

Blue nevi may represent an underrecognized risk factor for primary orbital melanoma, and enucleation may be preferable to evisceration for idiopathic corneal staphyloma to reduce melanoma risk.

## Linked entities

- **Proteins:** S100A1 (S100 calcium binding protein A1), PMEL (premelanosome protein)
- **Diseases:** proliferative vitreoretinopathy (MONDO:0100450)

## Full-text entities

- **Genes:** MLANA (melan-A) [NCBI Gene 2315] {aka MART-1, MART1}, S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}
- **Diseases:** tumor (MESH:D009369), melanoma (MESH:D008545), Blue nevi (MESH:D018329), congenital (MESH:D008209), congenital corneal staphyloma (MESH:D003316), proliferative vitreoretinopathy (MESH:D018630), blindness (MESH:D001766), metastasis (MESH:D009362), pigmented nevi (MESH:D009508)
- **Chemicals:** MEDPOR (MESH:C084562)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12813066/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12813066/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12813066/full.md

---
Source: https://tomesphere.com/paper/PMC12813066