# Oxaliplatin-induced porto-sinusoidal vascular disease manifesting as recurrent gastroesophageal variceal hemorrhage: a case report

**Authors:** Ruiqi Zhao, Chang Liang, Zhuoqing Zhuang, Yuan Xia, Junzhu Lu, Yan Zhang

PMC · DOI: 10.3389/fmed.2026.1772653 · Frontiers in Medicine · 2026-02-19

## TL;DR

A woman developed liver blood vessel disease after chemotherapy, causing severe bleeding and highlighting the need to consider this condition in similar cases.

## Contribution

This case report identifies oxaliplatin as a potential cause of porto-sinusoidal vascular disease in non-cirrhotic portal hypertension.

## Key findings

- A 44-year-old woman with colon cancer developed PSVD after oxaliplatin chemotherapy.
- Liver biopsy showed no cirrhosis, but portal hypertension and thrombosis were present.
- The case emphasizes the importance of recognizing PSVD in patients with non-cirrhotic portal hypertension.

## Abstract

Porto-sinusoidal vascular disease (PSVD) is an increasingly recognized cause of non-cirrhotic portal hypertension, characterized by structural abnormalities of the portal microvasculature and hepatic sinusoids in the absence of cirrhosis. Recognized predisposing factors include immune-mediated conditions, infections and exposure to hepatic sinusoid-toxic agents, among others. We report a 44-year-old woman with a history of oxaliplatin-based chemotherapy for colon cancer who presented with recurrent hematochezia, hematemesis, and transient encephalopathy. Evaluation demonstrated portal hypertension and portal vein thrombosis; however, liver biopsy showed no cirrhosis and the hepatic venous pressure gradient (HVPG) was within normal limits. Her medication history, combined with these findings, confirmed the diagnosis of oxaliplatin-induced PSVD. This case highlights the importance of considering PSVD in patients with non-cirrhotic portal hypertension, particularly when there is a history of exposure to agents toxic to the hepatic sinusoids, such as oxaliplatin.

## Linked entities

- **Chemicals:** oxaliplatin (PubChem CID 9887053)
- **Diseases:** colon cancer (MONDO:0002032), porto-sinusoidal vascular disease (MONDO:0035357), portal hypertension (MONDO:0005080), portal vein thrombosis (MONDO:0001339)

## Full-text entities

- **Genes:** PROC (protein C, inactivator of coagulation factors Va and VIIIa) [NCBI Gene 5624] {aka APC, PC, PROC1, THPH3, THPH4}, MPL (MPL proto-oncogene, thrombopoietin receptor) [NCBI Gene 4352] {aka C-MPL, CD110, MPLV, THCYT2, THPOR, TPOR}, BTG3 (BTG anti-proliferation factor 3) [NCBI Gene 10950] {aka ANA, ANA/BTG3, APRO4, TOB5, TOB55, TOFA}, SERPINC1 (serpin family C member 1) [NCBI Gene 462] {aka AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2}, CALR (calreticulin) [NCBI Gene 811] {aka CALR1, CRT, HEL-S-99n, RO, SSA, cC1qR}
- **Diseases:** chronic liver disease (MESH:D008107), gastroesophageal variceal bleeding (MESH:D014648), cirrhosis (MESH:D005355), autoimmune encephalitis (MESH:D020274), dysplasia (MESH:D015792), PSVD (MESH:D000094724), malignancy (MESH:D009369), pancytopenia (MESH:D010198), blood loss (MESH:D016063), hematemesis (MESH:D006396), splenomegaly (MESH:D013163), bleeding (MESH:D006470), esophageal variceal bleeding (MESH:D004932), Autoimmune disorders (MESH:D001327), fatigued (MESH:D005221), Thrombophilia (MESH:D019851), hypotension (MESH:D007022), hepatic sinusoidal endothelial injury (MESH:D006504), paraneoplastic (MESH:D010257), hypofibrinogenemia (MESH:D000347), hypoxia (MESH:D000860), portal hypertension (MESH:D006975), metabolic encephalopathy (MESH:D001928), palmar erythema (MESH:C565041), portal vein thrombosis (MESH:D012170), thrombosis (MESH:D013927), encephalopathy (MESH:D001927), CL (MESH:D002971), melena (MESH:D008551), hepatic parenchymal injury (MESH:D002543), colon cancer (MESH:D015179), hypersplenism (MESH:D006971), infections (MESH:D007239), immune disorders (MESH:D007154), thrombocytopenia (MESH:D013921), vascular injury (MESH:D057772), abdominal colic (MESH:D000007), Protein C deficiency (MESH:D020151), hepatitis (MESH:D056486), vascular liver disorder (MESH:D017093), immune dysregulation (OMIM:614878), spider angiomas (MESH:D006391), hyperplasia (MESH:D006965), autoimmune hepatitis (MESH:D019693), hypochromic anemia (MESH:D000747), gastrointestinal bleeding (MESH:D006471), memory loss (MESH:D008569), nodular regenerative hyperplasia (MESH:D020518)
- **Chemicals:** ammonia (MESH:D000641), bilirubin (MESH:D001663), carvedilol (MESH:D000077261), azathioprine (MESH:D001379), Oxaliplatin (MESH:D000077150), FEU (-), Hematoxylin (MESH:D006416), Rivaroxaban (MESH:D000069552), glutathione (MESH:D005978), Eosin (MESH:D004801)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** JAK2 V617F

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960632/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960632/full.md

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Source: https://tomesphere.com/paper/PMC12960632