Evidence map›Paper›PMID 42517041›Full record

ArticleFrontiers in medicine2026

Imaging features, diagnosis, and clinical management of hepatic involvement in hereditary hemorrhagic telangiectasia: a case series report and literature review.

Qiubo Feng, Qinpan Rao, Jiaqi Duan, Shufeng Fan, Linying Ma

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In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Qiubo FengDepartment of Radiology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Qinpan RaoDepartment of Radiology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Jiaqi DuanDepartment of Radiology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Shufeng Fan *Department of Radiology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Linying Ma *Department of Radiology, The Second Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To explore the clinical characteristics, imaging features, key diagnostic and therapeutic points, and risks of interventional therapy in hereditary hemorrhagic telangiectasia (HHT) with hepatic involvement, so as to improve the ability of clinicians and radiologists in the identification, diagnosis and treatment of this disease. A retrospective analysis was performed on the clinical data of 3 patients with HHT who were admitted to our hospital in the past 5 years and presented with predominant hepatic involvement. Their clinical symptoms, laboratory test results, imaging findings, and treatment outcomes were summarized, and a literature review was conducted for comprehensive analysis. All 3 patients met the Curacao diagnostic criteria for HHT and were found to have diffuse hepatic arteriovenous malformations, mainly presenting as mixed shunts. Computed tomography (CT) and magnetic resonance imaging (MRI) revealed dilated hepatic arteries, early visualization of the portal vein and hepatic vein, diffuse intrahepatic telangiectasias, and abnormal perfusion. One patient was complicated with biloma, and another was associated with portal hypertension and esophagogastric varices. Patient 3 underwent transcatheter hepatic arterial embolization (TAE) due to abdominal pain, and extensive thrombosis of the main portal vein and superior mesenteric vein occurred after the operation. Hepatic involvement in HHT is characterized by diffuse hepatic vascular malformations, with insidious clinical manifestations that are prone to misdiagnosis. Doppler ultrasound is the preferred screening method, while CT/MRI can comprehensively evaluate vascular malformations and related complications. Hepatic arterial embolization has a high risk of inducing portal vein thrombosis, and its routine application should be avoided in strict accordance with international guidelines. Clinicians need to strengthen medical history collection and multimodal imaging evaluation to reduce misdiagnosis and mistreatment.

Indexed as

computed tomographyhepatic arteriovenous malformationshepatic artery embolizationhereditary hemorrhagic telangiectasiamagnetic resonance imagingportal vein thrombosis

Identifiers

PMID42517041
PMCPMC13404187

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