Evidence map›Paper›PMID 41664979›Full record

ReviewJournal of cellular and molecular medicine2026

Snapshot Look at Castleman Disease.

Ciprian Jitaru, Natalia Zlampa, Delia Dima, Anca Bojan, Mihnea Zdrenghea, Laura Urian, David Kegyes, Anamaria Bancos, Maria Santa, Andrei Ivancuta and 8 more

Abstract readReview
In one paragraph

Review in Journal of cellular and molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Snapshot Look at Castleman Disease.Journal of cellular and molecular medicine · 2026
    Review
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.

Ciprian JitaruDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Natalia ZlampaDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Delia DimaDepartment of Hematology, Ion Chiricuta Oncology Institute, Cluj-Napoca, Romania.
Anca BojanDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.ORCID https://orcid.org/0000-0003-1523-3133
Mihnea ZdrengheaDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Laura UrianDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
David KegyesDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Anamaria BancosDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Maria SantaDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Andrei IvancutaDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Bobe PetrushevDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Madalina NistorDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Bogdan TiguDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Catalin ConstantinescuDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Bogdan FeticaDepartment of Hematology, Ion Chiricuta Oncology Institute, Cluj-Napoca, Romania.
Maria PuiuThe Genomics Research and Development Institute, Bucharest, Romania.
Mihai-Stefan MuresanDepartment of Surgery, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Ciprian TomuleasaDepartment of Personalized Medicine and Rare Diseases, Medfuture Institute for Biomedical Research, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.ORCID https://orcid.org/0000-0001-5500-1519

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Castleman disease (CD) is a rare and heterogeneous group of lymphoproliferative disorders characterised by abnormal proliferation of lymphoid tissue. First described in the 1950s, it has since been classified into two major clinical forms: unicentric CD (UCD), involving a single lymph node region and multicentric CD (MCD), which affects multiple regions and is often systemic. Further subclassification of MCD includes HHV8-associated MCD, POEMS-associated MCD and idiopathic MCD (iMCD), each with distinct pathophysiologic mechanisms and clinical implications. This review summarises current understanding of the epidemiology, clinical presentation, histopathology, pathogenesis and diagnostic challenges of CD. It also explores recent advances in molecular biology, including the role of interleukin-6 (IL-6), human herpesvirus-8 (HHV8) and aberrant immune signalling in disease progression. Therapeutic strategies vary significantly depending on the subtype and range from surgical resection in UCD to immunotherapy, siltuximab and cytotoxic chemotherapy in MCD. Despite progress, CD remains underdiagnosed and poorly understood, especially in its idiopathic forms. Continued research into its molecular underpinnings and targeted treatments is critical to improving patient outcomes and establishing evidence- based guidelines.

Indexed as

Castleman DiseaseAnimalsHerpesvirus 8, HumanHumansInterleukin-6Lymph NodesInterleukin-6Castleman diseaseneed‐to‐know information for the cliniciansnapshot look

Identifiers

PMID41664979
PMCPMC12887673

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.