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1.
Journal of Peking University(Health Sciences) ; (6): 521-529, 2023.
Artigo em Chinês | WPRIM | ID: wpr-986884

RESUMO

OBJECTIVE@#To analyze the clinicopathological features, molecular changes and prognostic factors in angioimmunoblastic T-cell lymphoma (AITL).@*METHODS@#Sixty-one cases AITL diagnosed by Department of Pathology of Peking University Cancer Hospital were collected with their clinical data. Morphologically, they were classified as typeⅠ[lymphoid tissue reactive hyperplasia (LRH) like]; typeⅡ[marginal zone lymphoma(MZL)like] and type Ⅲ [peripheral T-cell lymphoma, not specified (PTCL-NOS) like]. Immunohistochemical staining was used to evaluate the presence of follicular helper T-cell (TFH) phenotype, proliferation of extra germinal center (GC) follicular dendritic cells (FDCs), presence of Hodgkin and Reed-Sternberg (HRS)-like cells and large B transformation. The density of Epstein-Barr virus (EBV) + cells was counted with slides stained by Epstein-Barr virus encoded RNA (EBER) in situ hybridization on high power field (HPF). T-cell receptor / immunoglobulin gene (TCR/IG) clonality and targeted exome sequencing (TES) test were performed when necessary. SPSS 22.0 software was used for statistical analysis.@*RESULTS@#Morphological subtype (%): 11.4% (7/61) cases were classified as type Ⅰ; 50.8% (31/61) as type Ⅱ; 37.8% (23/61) as type Ⅲ. 83.6% (51/61) cases showed classical TFH immunophenotype. With variable extra-GC FDC meshwork proliferation (median 20.0%); 23.0% (14/61) had HRS-like cells; 11.5% (7/61) with large B transformation. 42.6% (26/61) of cases with high counts of EBV. 57.9% (11/19) TCR+/IG-, 26.3% (5/19) TCR+/IG+, 10.5% (2/19) were TCR-/IG-, and 5.3% (1/19) TCR-/IG+. Mutation frequencies by TES were 66.7% (20/30) for RHOA, 23.3% (7/30) for IDH2 mutation, 80.0% (24/30) for TET2 mutation, and 33.3% (10/30) DNMT3A mutation. Integrated analysis divided into four groups: (1) IDH2 and RHOA co-mutation group (7 cases): 6 cases were type Ⅱ, 1 case was type Ⅲ; all with typical TFH phenotype; HRS-like cells and large B transformation were not found; (2) RHOA single mutation group (13 cases): 1 case was type Ⅰ, 6 cases were type Ⅱ, 6 cases were type Ⅲ; 5 cases without typical TFH phenotype; 6 cases had HRS-like cells, and 2 cases with large B transformation. Atypically, 1 case showed TCR-/IG-, 1 case with TCR-/IG+, and 1 case with TCR+/IG+; (3) TET2 and/or DNMT3A mutation alone group (7 cases): 3 cases were type Ⅱ, 4 cases were type Ⅲ, all cases were found with typical TFH phenotype; 2 cases had HRS-like cells, 2 cases with large B transformation, and atypically; (4) non-mutation group (3 cases), all were type Ⅱ, with typical TFH phenotype, with significant extra-GC FDC proliferation, without HRS-like cells and large B transformation. Atypically, 1 case was TCR-/IG-. Univariate analysis confirmed that higher density of EBV positive cell was independent adverse prognostic factors for both overall survival (OS) and progression free survival(PFS), (P=0.017 and P=0.046).@*CONCLUSION@#Pathological diagnoses of ALTL cases with HRS-like cells, large B transformation or type Ⅰ are difficult. Although TCR/IG gene rearrangement test is helpful but still with limitation. TES involving RHOA, IDH2, TET2, DNMT3A can robustly assist in the differential diagnosis of those difficult cases. Higher density of EBV positive cells counts in tumor tissue might be an indicator for poor survival.


Assuntos
Humanos , Infecções por Vírus Epstein-Barr/genética , Herpesvirus Humano 4/genética , Linfócitos T Auxiliares-Indutores/patologia , Linfadenopatia Imunoblástica/patologia , Linfoma de Células T Periférico/patologia , Receptores de Antígenos de Linfócitos T
2.
IJFS-International Journal of Fertility and Sterility. 2014; 8 (1): 59-66
em Inglês | IMEMR | ID: emr-157597

RESUMO

Disorders in immune system regulation may result in pregnancy abnormalities such as recurrent spontaneous abortion [RSA]. This study aims to determine the ratio of regulatory T [Treg] and T helper [Th] 17 cells in unexplained RSA [URSA] women during proliferative and secretory phases of their menstrual cycles compared to healthy non-pregnant women. In this case control study, 25 women with URSA and 35 healthy, non-pregnant women were enrolled. The percentage of Th17 and Treg cells in participants peripheral blood were determined by flow cytometry. The percentage of Th17 cells and their related cytokines in serum [IL-17A] were higher in the proliferative and secretory phases of the menstrual cycles of URSA women compared to the control women. However, a lower percentage of Treg cells and their related cytokines in serum, transforming growth factor [TGF] beta1 and interleukin [IL]-10 were detected in the proliferative but not the secretory phase of the URSA group. The ratio of Th17/CD4+ Treg was higher in the URSA group than the control group. We observed an increased ratio of Th17/CD4+ Treg during the proliferative and secretory phases in URSA women. The imbalance between Th17 and Treg cells during the proliferative phase of menstrual cycles in the URSA group may be considered a cause for spontaneous abortion


Assuntos
Humanos , Feminino , Linfócitos T Reguladores/metabolismo , Fatores de Crescimento Transformadores , Linfócitos T Auxiliares-Indutores/metabolismo , Linfócitos T Auxiliares-Indutores/patologia , Linfócitos T Reguladores/patologia , Interleucina-17 , Ciclo Menstrual/imunologia , Estudos de Casos e Controles
3.
Arch. argent. dermatol ; 46(3): 123-7, mayo-jun. 1996. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-177415

RESUMO

Se presentan tres casos de infiltración linfocítica de la piel. Se describen las características clínicas, se realizan tomas biopsias que confirman el diagnóstico, e inmunomarcación que muestra predominio de linfocitos T. Se hacen los diagnósticos diferenciales concluyendo que esta afección dermatológica puede presentarse con diferentes aspectos clínicos, algunos totalmente atípicos. Es en estos casos donde la histopatología y la inmunomarcación confirman el diagnóstico


Assuntos
Humanos , Masculino , Adulto , Pessoa de Meia-Idade , Imuno-Histoquímica/tendências , Leucemia Linfocítica Crônica de Células B/diagnóstico , Dermatopatias Papuloescamosas/patologia , Linfócitos T Auxiliares-Indutores/patologia , Linfócitos T/imunologia , Complexo Antígeno-Anticorpo , Diagnóstico Diferencial , Hidroxicloroquina/uso terapêutico , Dermatopatias Papuloescamosas/tratamento farmacológico , Linfócitos T Auxiliares-Indutores/patologia , Talidomida/uso terapêutico
4.
An. bras. dermatol ; 61(5): 237-9, set.-out. 1986. ilus
Artigo em Português | LILACS | ID: lil-37217

RESUMO

Apresenta-se um caso de papulose linfomatóide, que é o primeiro caso observado no Serviço de Dermatologia do Hospital Central do IASERJ e a primeira comunicaçäo feita no Brasil


Assuntos
Idoso , Humanos , Feminino , Células de Langerhans/patologia , Úlcera Cutânea/patologia , Linfócitos T Auxiliares-Indutores/patologia
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