Evidence map›Paper›PMID 37924345›Full record

ArticleVirchows Archiv : an international journal of pathology2024

Erythrophagocytosis is not a reproducible finding in liver biopsies, and is not associated with clinical diagnosis of hemophagocytic lymphohistiocytosis.

Niyati Desai, Satoru Kudose, Helen E Remotti, Armando Del Portillo, Ladan Fazlollahi, Michael J Lee, Yuqing Xiong, Roger K Moreira, Marcela Salomao, Maria Isabel Fiel and 8 more

Abstract read
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Article in Virchows Archiv : an international journal of pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 34% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 11 institutions in 2 countries.

Niyati DesaiDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, 622 W 168th St.VC14-209A, New York, NY, 10032, USA.
Satoru KudoseDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, 622 W 168th St.VC14-209A, New York, NY, 10032, USA.
Helen E RemottiDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, 622 W 168th St.VC14-209A, New York, NY, 10032, USA.
Armando Del PortilloDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, 622 W 168th St.VC14-209A, New York, NY, 10032, USA.
Ladan FazlollahiDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, 622 W 168th St.VC14-209A, New York, NY, 10032, USA.
Michael J LeeDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, 622 W 168th St.VC14-209A, New York, NY, 10032, USA.
Yuqing XiongDepartment of Pathology, Mass General Brigham, Boston, MA, USA.
Roger K MoreiraDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Marcela SalomaoDepartment of Pathology, Mayo Clinic, Scottsdale, AZ, USA.
Maria Isabel FielDepartment of Pathology, Mount Sinai School of Medicine, New York, NY, USA.
Raul S GonzalezDepartment of Pathology and Laboratory Medicine, Emory University Hospital, Atlanta, USA.
Joseph MisdrajiDepartment of Pathology, Yale University, New Haven, USA.
Ryan M GillDepartment of Pathology, University of California, San Francisco, San Francisco, USA.
John HartDepartment of Pathology, University of Chicago, Chicago, USA.
David E KleinerLaboratory of Pathology, National Cancer Institute, Bethesda, USA.
Uta DrebberInstitute of Pathology, University Hospital of Cologne, Cologne, Germany.
Andrew M BellizziDepartment of Pathology, University of Iowa, Iowa City, USA.
Stephen M LaganaDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, 622 W 168th St.VC14-209A, New York, NY, 10032, USA. SML2179@cumc.columbia.edu.ORCID http://orcid.org/0000-0002-1533-368X
Columbia University Irving Medical Center · USMayo Clinic in Arizona · USEmory University Hospital · USIcahn School of Medicine at Mount Sinai · USMass General Brigham · USNational Cancer Institute · USUniversity Hospital Cologne · DEUniversity of California, San Francisco · USUniversity of Chicago · USUniversity of Iowa · USYale University · US

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Mark E Burkard · 2000 to 2026
$70.0M
Postmortem PathologyZICBC010685 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KLEINER, DAVID ERWIN · 2009 to 2025
$14.3M
NCI NIH HHS P30 CA086862
6 · The paper itself

Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a rare disease with high mortality. Liver involvement is common (based on elevated liver function tests) with most patients demonstrating acute hepatitis. Liver biopsies are frequently obtained in the setting of suspected HLH for the purpose of identification of erythrophagocytosis, and if present, this finding is thought to suggest or support the diagnosis of HLH. However, there are problems with this approach; in particular, we do not know whether this finding is reproducible or whether it is specific to HLH. Therefore, we conducted a multi-institutional study in which experienced liver pathologists reviewed images taken from liver biopsies from patients with normal liver, acute hepatitis, possible HLH, and clinical HLH to determine if there was agreement about the presence or absence of erythrophagocytosis, and to ascertain whether the finding corresponds to a clinical diagnosis of HLH. Twelve liver pathologists reviewed 141 images in isolation (i.e., no clinical information or diagnosis provided). These came from 32 patients (five normal, 17 acute hepatitis, six HLH, four possible HLH). The pathologists classified each image as negative, equivocal, or positive for erythrophagocytosis. Kappa was .08 (no agreement) for case-level and 0.1 for image-level (1.4% agreement, based on two images which were universally considered negative). There was no difference in the proportion of pathologists who diagnosed erythrophagocytosis among those with different diagnoses at case or image-level (p = 0.82 and p = 0.82, respectively). Thus, erythrophagocytosis is an entirely unreliable histologic parameter in liver, as it is irreproducible and not demonstrably associated with a clinical disease (namely, HLH). Unless and until more reliable guidelines can be established, pathologists should refrain from commenting on the presence or absence of erythrophagocytosis in liver biopsy.

Indexed as

HepatitisLymphohistiocytosis, HemophagocyticAcute DiseaseBiopsyHumansErythrophagocytosisHemophagocytic lymphohistiocytosisInterobserver variabilityLiver pathology

Identifiers

PMID37924345
OpenAlexW4388342872

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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.