# Trastuzumab Emtansine (T-DM1)-Induced Porto-Sinusoidal Vascular Disorder: A Case Report

**Authors:** Catarina L Fernandes, Orlando Pedro, Filipe Andrade, Monica Pinho

PMC · DOI: 10.7759/cureus.86333 · 2025-06-19

## TL;DR

A patient with HER2-positive breast cancer developed a rare liver condition called PSVD after treatment with T-DM1, highlighting the need for awareness and early diagnosis.

## Contribution

This case report documents a rare complication of T-DM1 treatment and emphasizes the importance of clinical suspicion for diagnosis.

## Key findings

- PSVD is a rare but possible complication of T-DM1 treatment in HER2-positive breast cancer patients.
- Clinical suspicion and liver biopsy are essential for diagnosing PSVD.
- Discontinuation of T-DM1 is the only known treatment for PSVD.

## Abstract

T-DM1 is used to treat early and advanced HER2-positive breast cancer and has a favorable toxicity profile. Porto-sinusoidal vascular disorder (PSVD) is a rare complication of this treatment, and its pathophysiology is not fully understood. A 43-year-old female patient was diagnosed with locally advanced HER2-overexpressing breast cancer, treated with primary chemotherapy, followed by surgery and adjuvant radiotherapy and trastuzumab. Distant relapse was identified four years later, and T-DM1 was started, leading to a complete response. Given the alterations in liver enzymes and signs of portal hypertension observed in a CT scan, a liver biopsy was performed, revealing lesions compatible with PSVD. PSVD related to T-DM1 was assumed, T-DM1 was suspended, and the patient remained under surveillance. She remained asymptomatic and with no evidence of disease for seven months. T-DM1-related PSVD is a rare complication of T-DM1 treatment that should not be overlooked. Clinical suspicion is essential for diagnosis, and T-DM1 suspension is the only known treatment.

## Linked entities

- **Proteins:** ERBB2 (erb-b2 receptor tyrosine kinase 2)
- **Diseases:** breast cancer (MONDO:0004989), portal hypertension (MONDO:0005080)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** toxicity (MESH:D064420), T-DM1 (MESH:D009223), PSVD (MESH:D000094724), portal hypertension (MESH:D006975), breast cancer (MESH:D001943), positive (MESH:D000377)
- **Chemicals:** trastuzumab (MESH:D000068878), T-DM1 (MESH:D000080044)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12274956/full.md

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Source: https://tomesphere.com/paper/PMC12274956