# A rare case of vision loss caused by leptomeningeal metastasis of lung adenocarcinoma: a case report and literature review

**Authors:** Zhihua Li, Jian Chu, Wennan Shen, Junnan Chen, Yuemei Dong, Manze Zhang, Nan Zhao, Wei Zhao, Haoran Zha, Ning Wang, Yalin Han, Zhaoxia Li

PMC · DOI: 10.3389/fonc.2025.1484383 · 2025-02-10

## TL;DR

A rare case of lung cancer causing vision loss through brain metastasis was successfully treated with a targeted drug after detecting a specific mutation.

## Contribution

This case highlights the survival benefit of trametinib in treating leptomeningeal metastasis with BRAF non-V600E mutations.

## Key findings

- A patient with LM from lung cancer experienced vision loss and responded to trametinib treatment.
- BRAF non-V600E mutation detection in CSF guided effective targeted therapy.
- Literature review suggests improved survival with CSF chemotherapy and MEK inhibitors in similar cases.

## Abstract

Leptomeningeal metastasis (LM) is a fatal complication with increasing incidence in patients with non-small cell lung cancer. Herein, we present the case of a patient who presented with complete vision loss due to LM and achieved a survival benefit from treatment with trametinib. The treatment was prescribed based on the detection of a BRAF non-V600E mutation in the cerebrospinal fluid (CSF). We reviewed the literature and evaluated survival benefits in patients with LM harboring BRAF non-V600E mutations treated with CSF chemotherapy and mitogen-activated extracellular signal-regulated kinase inhibitors.

## Linked entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673]
- **Chemicals:** trametinib (PubChem CID 11707110)
- **Diseases:** lung adenocarcinoma (MONDO:0005061), leptomeningeal metastasis (MONDO:0700219)

## Full-text entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}
- **Diseases:** non-small cell lung cancer (MESH:D002289), lung adenocarcinoma (MESH:D000077192), vision loss (MESH:D014786), LM (MESH:D009362)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** V600E

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11847661/full.md

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Source: https://tomesphere.com/paper/PMC11847661