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[Clinicopathological features of angioimmunoblastic T-cell lymphoma pattern Ⅰ]
1Department of Pathology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
Diagnosing angioimmunoblastic T-cell lymphoma pattern Ⅰ (AITL Pattern Ⅰ) is challenging. Comprehensive analysis of clinical, histological, immunophenotypic, and genetic data is crucial for accurate diagnosis.
Area of Science:
- Hematopathology
- Oncology
- Immunology
Background:
- Angioimmunoblastic T-cell lymphoma (AITL) is an aggressive non-Hodgkin lymphoma.
- AITL Pattern Ⅰ presents unique diagnostic challenges.
- Accurate diagnosis is critical for appropriate patient management.
Purpose of the Study:
- To investigate the clinicopathological features of AITL Pattern Ⅰ.
- To identify key diagnostic markers for AITL Pattern Ⅰ.
- To improve diagnostic accuracy for this specific lymphoma subtype.
Main Methods:
- Retrospective analysis of 11 AITL Pattern Ⅰ cases.
- Evaluation of clinicopathological data, including immunophenotype and Epstein-Barr virus (EBV) status.
- Testing of T cell receptor (TCR) clonality and histological morphology.
Main Results:
- AITL Pattern Ⅰ cases exhibited specific histological findings, including hyperplastic follicles and atypical lymphocytes.
- Immunohistochemistry revealed characteristic expression patterns of CD3, CD4, PD-1, CXCL13, ICOS, and CD10.
- All cases showed monoclonal T cell receptor gene rearrangement and scattered EBV-encoded small RNA (EBER) positive B lymphocytes.
Conclusions:
- Diagnosing AITL Pattern Ⅰ requires a multidisciplinary approach.
- Integration of clinical, histological, immunophenotypic, and molecular data is essential.
- This study highlights the complexity and diagnostic criteria for AITL Pattern Ⅰ.
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