Evidence map›Paper›PMID 41957927›Full record

ArticleThe American journal of surgical pathology2026

Segmental Atrophy of the Liver: An Increasingly Recognized Pseudotumor With Distinct Clinicopathologic and Imaging Features.

Lakhdar Khellaf, Aude Trinquet, Olivia Sgarbura, François Quénet, Stéphanie Nougaret

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Article in The American journal of surgical pathology, 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

What it found

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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

5 authors.

Lakhdar KhellafDepartment of Pathology.ORCID 0000-0001-7107-3280
Aude TrinquetDepartment of Pathology, University Hospital of Montpellier, Montpellier, Cedex, France.
Olivia SgarburaDepartment of Oncological Surgery.
François QuénetDepartment of Oncological Surgery.
Stéphanie NougaretDepartment of Radiology, Montpellier Cancer Institute, Montpellier, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Segmental atrophy of the liver (SAL) is a recently described vascular-related pseudotumor. We report a series of 26 SAL cases in cancer patients, highlighting clinical, pathologic, and imaging features, with insights into pathogenesis. Cases were prospectively collected between 2017 and 2023 at the Montpellier Cancer Institute. Lesion staging, vascular lesions, and extralesional changes were systematically assessed, with immunohistochemical analysis. All patients (mean age 68 y; female-to-male ratio 1.7) were under oncologic follow-up; 46% had cardiovascular disease and/or diabetes. The median lesion size was 14 mm. Obliterative thrombosis was identified in 14 of 16 evaluable surgical specimens (88%), involving arteries, veins, or both, with intralesional and/or perilesional distribution. Arteriolar hyperplasia was present in 50% of cases, predominantly in advanced lesions, and showed a nonsignificant trend toward higher prevalence in bevacizumab-treated patients. Sinusoidal obstruction syndrome was observed in 31% of cases. Local contributing factors included prior liver-directed therapy (12% of patients) and concurrent tumor involvement (37% of patients), occasionally suggesting tumor-related vascular compression. We identified SMA-positive stromal cells clustered around small- and medium-sized vessels, supporting a perivascular origin and implicating thrombotic vascular injury in fibroelastotic remodeling. These findings highlight the contribution of both local and systemic factors to vascular injury underlying SAL. Recognition of this pseudotumor is essential to avoid misinterpretation and inappropriate clinical management.

Indexed as

Granuloma, Plasma CellLiverLiver DiseasesLiver NeoplasmsAdultAgedAged, 80 and overAtrophyFemaleHumansMaleMiddle AgedProspective Studieshepatic pseudotumormyofibroblastspathogenesissegmental atrophy of the liversinusoidal obstruction syndromesynchronous liver tumorsthrombosis

Identifiers

PMID41957927
PMCPMC13263046

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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.