Evidence map›Paper›PMID 41943429›Full record

ArticleThe American journal of case reports2026

Mycosis Fungoides With Large Cell Lymphoma Transformation: A Report of a Rare Case.

Miguel Augusto Martins Pereira, João Vitor Madureira Bronzo, Noémie Fourcroy Maillard, Luciana Pantaleão

Abstract readCase Reports
In one paragraph

Article in The American journal of case reports, 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

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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

The trial behind it

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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

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

4 authors.

Miguel Augusto Martins PereiraDepartment of Pathology, Universidade Federal Fluminense (UFF), Niterói, RJ, Brazil.ORCID 0000-0001-5646-2253
João Vitor Madureira BronzoMedical School, Universidade Federal Fluminense (UFF), Niterói, RJ, Brazil.ORCID 0009-0009-8868-0146
Noémie Fourcroy MaillardMedical School, Universidade Federal Fluminense (UFF), Niterói, RJ, Brazil.ORCID 0009-0003-7616-6031
Luciana PantaleãoDepartment of Pathology, Universidade Federal Fluminense (UFF), Niterói, RJ,, Brazil.ORCID 0000-0001-7480-2530

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Mycosis fungoides, the most common cutaneous T-cell lymphoma, can transform into large cell lymphoma in some cases, leading to worse outcomes and reduced life expectancy. CASE REPORT We report the case of a 38-year-old Brazilian man with a history of multiple skin lesions refractory to medical treatment, requiring repeated hospitalizations, procedures, chemotherapy, phototherapy, and immunotherapy. The patient was followed by the same hospital's pathology and dermatology services for 17 years, from the diagnosis of mycosis fungoides to subsequent transformation to large cell lymphoma and eventual death. CONCLUSIONS We report a rare condition with a poor prognosis, highlighting the challenges associated with disease transformation, which markedly reduces patients' life expectancy and quality of life. The histological findings and association with the clinical manifestations were vital to the diagnosis and treatment of the disease; thus, early biopsy - even in young patients - is recommended, as it may reveal a new differential diagnosis and influence prognosis. Since the evolution of mycosis fungoides to large cell lymphoma after the transformation process is extremely aggressive, we emphatically recommend initial and follow-up biopsies even in younger patients without prior comorbidities, as in the present case. Increased awareness among clinicians regarding atypical presentations, particularly in populations not typically considered at risk, such as our patient, may also contribute significantly to timely intervention and more favorable outcomes.

Indexed as

Cell Transformation, NeoplasticLymphoma, Large B-Cell, DiffuseMycosis FungoidesSkin NeoplasmsAdultBiopsyFatal OutcomeHumansMaleSkin

Identifiers

PMID41943429
PMCPMC13069906

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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.