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September 10, 2025

Monomorphic epitheliotropic intestinal T-cell lymphoma: a clinicopathological and genetic mutation characteristics analysis of forty-two cases.

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Authors

DFDage FanFujian Medical UniversityYWY Z WangBaoshan CollegeALA Q LiRuijin Hospital

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Implication

Retrospective analysis identifies genetic mutations and immunohistochemical profiles in MEITL, suggesting poor prognosis.

Key Points

  • MEITL exhibited a high mortality rate of 93.1% among follow-up cases, highlighting its aggressive nature.
  • Targeted next-generation sequencing detected mutations in genes like SETD2 and TP53 in MEITL patients, indicating genetic complexity.
  • Immunohistochemistry showed high expression of T-cell markers in MEITL specimens, aiding in diagnosis.
  • Clinical characteristics varied widely, but diagnosis relied on integrating morphological analysis, genetic testing, and EBV status.

Cite This Study

Fan et al. (2025) studied this question.

synapsesocial.com/papers/68d413f8713b0b5dfea61b04https://doi.org/10.3760/cma.j.cn112151-20250217-00105
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1[Atypical clinicopathological features of monomorphic epitheliotropic intestinal T-cell lymphoma].2025 · 1 citations
  2. 2A Lethal Case of Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma Presented as Asymptomatic Colonic Ulcer2025
  3. 3Concurrent monomorphic epitheliotropic intestinal T-cell lymphoma with aberrant CD20 expression and lung adenocarcinoma: A case report and literature review2026
  4. 4Leptomeningitis as Rare Secondary Dissemination in MEITL (Monomorphic Intestinal Epitheliotropic T-Cell Lymphoma)2025 · 1 citations
  5. 5Case-Based Insights into Enteropathy-Associated T-Cell Lymphoma—Single-Center Experience2025 · 1 citations