Evidence map›Paper›PMID 41660154›Full record

ArticlePathology oncology research : POR2026

Assessment of the prevalence and consistency of microvascular flow imaging patterns in focal nodular hyperplasia.

Boglárka Zsély, Aladár Dávid Rónaszéki, Marco Himsel, Zita Zsombor, Gabriella Győri, Anikó Folhoffer, Dorottya Mühl, Viktor Bérczi, Byung-So Park, Damján Pekli and 4 more

Abstract read
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Article in Pathology oncology research : POR, 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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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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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

14 authors.

Boglárka ZsélyMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Aladár Dávid RónaszékiMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Marco HimselMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Zita ZsomborMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Gabriella GyőriMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Anikó FolhofferDepartment of Internal Medicine and Oncology, Semmelweis University, Budapest, Hungary.
Dorottya MühlDepartment of Internal Medicine and Oncology, Semmelweis University, Budapest, Hungary.
Viktor BércziMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Byung-So ParkSamsung Medison Co Ltd., Gangnam-gu, Republic of Korea.
Damján PekliDepartment of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.
Oszkár HahnDepartment of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.
András KissDepartment of Pathology, Forensic and Insurance Medicine, Semmelweis University, Budapest, Hungary.
Pál Maurovich-HorvatMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Pál Novák KaposiMedical Imaging Centre, Semmelweis University, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To identify characteristic vascular features of focal nodular hyperplasia (FNH) on microvascular flow imaging (MVFI) and assess the utility of MVFI in FNH diagnosis. Methods: This retrospective study included B-mode ultrasound (US) and MVFI scans of 41 FNHs, 21 hepatocellular carcinomas (HCCs), 20 metastases (METs), 10 hepatocellular adenomas (HCAs), and eight hemangiomas (HEMs) from 80 patients. Diagnoses were confirmed by contrast-enhanced imaging or histology. Two independent observers evaluated vascular patterns on MVFI. Interobserver agreement was calculated, and logistic regression models using either B-mode or MVFI features were developed to differentiate FNH from other focal liver lesions (FLLs). Results: Interobserver agreement for MVFI patterns was substantial (κ = 0.641, p < 0.001). The spoke-wheel pattern (OR = 51.53 and 35.28) and central artery (OR = 4.96 and 1.95) were strongly associated with FNH. However, the spoke-wheel pattern also appeared in subsets of HCAs (20%-30%), HCCs (14%-19%), and METs (5%-15%). Rim vascularity was common but nonspecific. The MVFI-based model (AUC = 0.891, p < 0.001) outperformed the B-mode model (AUC = 0.814) in distinguishing FNH. For lesions ≥3 cm, MVFI accuracy was even higher (AUC = 0.944, p < 0.001). Conclusion: MVFI enhances the diagnostic confidence of US for FNH, particularly in asymptomatic patients at low risk for malignancy. However, given the potential overlap with certain malignant FLLs, MVFI findings should be interpreted with caution.

Indexed as

Carcinoma, HepatocellularFocal Nodular HyperplasiaHemangiomaLiver NeoplasmsMicrovesselsAdultAgedFemaleHumansMaleMiddle AgedPrevalencePrognosisRetrospective StudiesUltrasonographydoppler ultrasonographyfocal nodular hyperplasialivermicrovascular imagingultrasound

Identifiers

PMID41660154
PMCPMC12875999

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.