Evidence map›Paper›PMID 40900230›Full record

ArticleVirchows Archiv : an international journal of pathology2026

Skin manifestations uncover underlying Follicular helper T-cell lymphoma, angioimmunoblastic-type in an immunosuppressed patient.

Marie-Laure García, Rebeca Manso, Juan Torre Castro, Lucía Pavía Pascual, Sergio Ramos Cillán, Daniel Morillo, Juan Carlos Caballero Hernaez, Fina Climent, Luis Requena, Socorro María Rodríguez Pinilla and 1 more

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In one paragraph

Article 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. 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. Article
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

11 authors.

Marie-Laure GarcíaPathology Department, Hospital Universitario de Cáceres, 10004, Cáceres, Spain.
Rebeca MansoPathology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Juan Torre CastroDermatology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Lucía Pavía PascualHematology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Sergio Ramos CillánHematology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Daniel MorilloHematology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Juan Carlos Caballero HernaezHematology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Fina ClimentPathology Department, Bellvitge University Hospital, Barcelona, Spain.
Luis RequenaDermatology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Socorro María Rodríguez PinillaPathology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain.
Francisco Javier Díaz de la PintaPathology Department, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), 28040, Madrid, Spain. fjavier.diazp@quironsalud.es.ORCID http://orcid.org/0000-0002-7070-0550

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the context of immunosuppression, most lymphoproliferative disorders are of B-cell origin and associated with Epstein-Barr virus (EBV). Follicular Helper T-cell Lymphoma, Angioimmunoblastic type (AITL) is the most frequently encountered T-cell lymphoma subtype. We present a challenging AITL case, initially misinterpreted as a polymorphic EBV + B-cell lymphoma, in a 62-year-old woman with a history of rheumatoid arthritis treated with multiple immunosuppressive agents. Over several years, she developed varied cutaneous manifestations with distinct histopathological infiltration patterns, prompting a diagnostic reassessment. Molecular studies demonstrated T-cell clonality, and RHOA and TET2 mutations, supporting the diagnosis of AITL with associated EBV + B-cell expansion. Notably, the presence of epidermotropic EBV + B-cell infiltrates masked the underlying T-cell neoplasm. This case underscores the importance of integrating histopathological, clinical, and molecular data, and highlights the diagnostic and biological complexity of AITL, particularly when it arises in the setting of immune dysregulation and exhibits features overlapping with EBV-driven B-cell proliferations.

Indexed as

Immunoblastic LymphadenopathyImmunocompromised HostLymphoma, FollicularLymphoma, T-CellLymphoma, T-Cell, CutaneousSkin NeoplasmsT Follicular Helper CellsT-Lymphocytes, Helper-InducerArthritis, RheumatoidFemaleHumansImmunosuppressive AgentsMiddle AgedImmunosuppressive AgentsAngioimmunoblastic T-cell lymphomaCutaneous T-cell lymphomaImmunosupresionNext-generation sequencing

Identifiers

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Registered trials

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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.