Evidence map›Paper›PMID 40210741›Full record

ReviewVirchows Archiv : an international journal of pathology2026

Histiocytoses and reactive proliferations of histiocytes: current state of the art and evolving concepts-a report from the joint CSHP-EA4HP-SH workshop 2024, Hefei, China.

Falko Fend, Stefan Dirnhofer, Caoimhe Egan, Sophie Song, Zhe Wang, Xiaoqiu Li, Weiping Liu, Wenbin Xiao, Jean-Francois Emile, John Goodlad and 1 more

Abstract readReview
In one paragraph

Review in Virchows Archiv : an international journal of 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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0citing papers in PubMed
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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

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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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors.

Falko FendInstitute of Pathology and Neuropathology and Comprehensive Cancer Center, Tübingen University Hospital, Liebermeisterstrasse 8, 72076, Tübingen, Germany. falko.fend@med.uni-tuebingen.de.ORCID http://orcid.org/0000-0002-5496-293X
Stefan DirnhoferPathology, Institute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
Caoimhe EganHaematopathology & Oncology Diagnostic Service, Cambridge University Hospitals, NHS Foundation Trust, Cambridge, UK.
Sophie SongDepartment of Pathology and Laboratory Medicine, UCLA Health/David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Zhe WangDepartment of Pathology, Xijing Hospital and School of Basic Medicine, Fourth Military Medical University, Xi'an, People's Republic of China.
Xiaoqiu LiDepartment of Pathology, Shanghai Cancer Center, Fudan University, Shanghai, People's Republic of China.
Weiping LiuDepartment of Pathology, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
Wenbin XiaoDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Jean-Francois EmileParis-Saclay University, Versailles SQY University, EA4340-BECCOH, Assistance Publique-Hôpitaux de Paris (AP-HP), Ambroise-Paré Hospital, Smart Imaging, Service de Pathologie, Boulogne, France.
John GoodladDepartment of Pathology, NHS Greater Glasgow and Clyde, Glasgow, Great Britain.
Robert LorsbachDepartment of Pathology and Laboratory Medicine, Cincinnati Children'S Hospital Medical Center, University of Cincinnati, 3333 Burnett Avenue MLC 1035, Cincinnati, OH, 45229, USA. robert.lorsbach@cchmc.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reactive and clonal proliferations of histiocytes (macrophages/dendritic cells) represent a broad spectrum of disorders, which can affect virtually any organ of the body. The clinical spectrum ranges from benign, localized and self-limiting manifestations to severe multi-system disease. Hemophagocytic lymphohistiocytosis (HLH) is a frequently life-threatening, systemic hyperinflammatory process triggered by massive cytokine release by activated, reactive macrophages. Familial and secondary forms of HLH are discerned. Histiocytoses are clonal inflammatory myeloid disorders characterized by proliferations of mature histiocytes/macrophages and dendritic cells with recurrent kinase-activating mutations which result in constitutive activation of the ERK signaling pathway. Although traditionally subclassified according to the phenotype of the lesional cells, the clonal cells can show significant plasticity, and the occurrence of mixed histiocytoses is increasingly recognized. This is in part due to their derivation from a myeloid progenitor cell and explains the frequent association with clonal hematopoiesis or overt myeloid neoplasms in adults. At the joint Workshop of the Chinese Society of Hematopathology, the European Association for Haematopathology and the Society for Hematopathology on histiocytic/dendritic cell proliferations, neoplasms, and their mimics in Hefei, China, April 2024, in sessions 1 and 2 a total of 8 cases of HLH, 9 cases of reactive histiocytic proliferations and 40 cases of histiocytoses were submitted and reviewed by the panel. The latter included cases of LCH, indeterminate cell histiocytosis, Erdheim Chester disease, juvenile xanthogranuloma, Rosai Dorfman disease, multicentric reticulohistiocytosis, ALK-positive histiocytosis, and mixed histiocytoses. The present report summarizes important findings and open questions arising from discussing the workshop cases.

Indexed as

Cell ProliferationHistiocytesHistiocytosisLymphohistiocytosis, HemophagocyticChinaDendritic CellsHumansClassification of histiocytic disordersHemophagocytic lymphohistiocytosisHistiocytosisJoint workshop

Identifiers

PMID40210741
PMCPMC12916990

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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.