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[Angioimmunoblastic T-cell lymphoma: histopathological grading and prognosis].
Guo, Y M; Liu, X F; Jiao, L J; Yin, S Y; Wang, Z; Li, X X; Ma, Z P; Yang, J M; He, M X.
Afiliação
  • Guo YM; Department of Pathology, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China; Department of Pathology, Shanghai Baoshan District Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai 201900, China.
  • Liu XF; Department of Pathology, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China.
  • Jiao LJ; Department of Pathology, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China.
  • Yin SY; Department of Pathology, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China.
  • Wang Z; Department of Pathology, Xijing Hospital, Air Force Military Medical University, Xi'an, 710032, China.
  • Li XX; Department of Pathology, the First Affiliated Hospital, Xinjiang Medical University, Urumqi 830054, China.
  • Ma ZP; Department of Pathology, the First Affiliated Hospital, Xinjiang Medical University, Urumqi 830054, China.
  • Yang JM; Department of Hematology, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China.
  • He MX; Department of Pathology, Changhai Hospital, Naval Military Medical University, Shanghai 200433, China.
Zhonghua Bing Li Xue Za Zhi ; 48(10): 784-790, 2019 Oct 08.
Article em Zh | MEDLINE | ID: mdl-31594043
ABSTRACT

Objective:

To investigate the histological features and prognostic factors of angioimmunoblastic T-cell lymphoma (AITL).

Methods:

The pathological data of 62 patients with AITL with complete follow-up information were retrospectively collected and analyzed from Changhai Hospital during September 2012 and September 2017. Histological and immunohistochemical (IHC) examination, in situ hybridization (ISH), and single nucleotide polymorphisms (SNP) gene mutation analysis were done. Subgroup evaluation with histology, IHC, ISH, SNP gene mutation, and association with clinical progression were performed.

Results:

The cohort included 62 cases of AITL, including 46 males and 16 females patients, with a median age of 64 years. Follicular dendritic cells (FDC) area showed significantly expansion (≥30%) in 40 cases; increased plasma cells (≥10%) was seen in 37 cases; B cells were distributed around blood vessels in 37 cases; and increased p53 mutation positive cells (≥40%) were seen in 39 cases; high Ki-67 index (≥40%) was seen in 39 cases; RHOA mutation was seen in 19 cases; TET2 mutation was seen in 9 cases. Overall survival analysis showed these factors were significantly correlated with tumor prognosis (P<0.05). Multivariate analysis showed that CD38 positive cells<10%, Ki-67≥40%, RHOA and TET2 mutations were risk factors associated with overall survival.

Conclusions:

AITL could be divided into two different prognostic groups, low-grade and high-grade, with statistically significance outcome, based on the FDC area expansion, degree of plasma cell proliferation, B cells distribution pattern combined with gene mutations and clinical progression. Low-grade malignant group progresses slowly, and high-grade malignant group is highly invasive.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Células T / Linfadenopatia Imunoblástica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Células T / Linfadenopatia Imunoblástica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: Zh Ano de publicação: 2019 Tipo de documento: Article