首页> 美国卫生研究院文献>International Journal of Clinical and Experimental Pathology >Primary mucosal CD30-positive T-cell lymphoproliferative disorders of the head and neck rarely involving epiglottis: clinicopathological immunohistomchemical and genetic features of a case
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Primary mucosal CD30-positive T-cell lymphoproliferative disorders of the head and neck rarely involving epiglottis: clinicopathological immunohistomchemical and genetic features of a case

机译:头颈部很少见到会厌的原发性黏膜CD30阳性T细胞淋巴组织增生性疾病:一例的临床病理免疫组织化学和遗传学特征

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摘要

A case of primary mucosal CD30-positive T-cell lymphoproliferative disorder of the head and neck rarely involving epiglottis in a 59-year-old male was reported. Histologically, the ulcerative mucosa was affected by sheets of mixed inflammatory infiltration, with scattered large atypical lymphoid cells arranging in an individual or small clusters with focal epidermotropism. Immunohistochemically, tumor cells were uniformly immunoreactive to antibodies against CD2, CD3, CD7, CD43, CD4, TIA-1, with a heterogeneous expression of CD30, but negative for CD20, CD79a, CD21, CD8, CD56, ALK, EMA, granzyme B. Epstein-Barr virus encoded RNA (EBER) were detected. Genetically, T-cell receptor (TCR) γ gene showed an oligoclonal rearrangement. This first case developing in epiglottis demonstrates mucosal CD30-positive T-cell lymphoproliferative disorders are characteristic of a broad clinicopathologic spectrum similar to the counterpart in the skin with a favorable prognosis.
机译:据报道,一例59岁男性的头颈部原发性粘膜CD30阳性T细胞淋巴组织增生性疾病很少涉及会厌。从组织学上看,溃疡性黏膜受混合的炎性浸润影响,散在的大的非典型淋巴样细胞排列成单个或小的簇,具有局灶性表皮生长。免疫组织化学分析,肿瘤细胞对CD2,CD3,CD7,CD43,CD4,TIA-1抗体具有均一的免疫反应性,但CD30异质表达,但CD20,CD79a,CD21,CD8,CD56,ALK,EMA,粒酶B阴性检测到爱泼斯坦-巴尔病毒编码的RNA(EBER)。遗传上,T细胞受体(TCR)γ基因表现出寡克隆重排。在会厌中发展的第一例病例表明,粘膜CD30阳性T细胞淋巴增生性疾病具有广泛的临床病理特征,与皮肤对应物相似,预后良好。

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