nk细胞淋巴瘤讲义PPT文档

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1、包括:1.结外NK/T细胞淋巴瘤,鼻型2.侵袭性NK细胞白血病3.慢性NK细胞淋巴增生性疾病NK细胞的免疫表型特点No single marker unequivocally identifies all NK cellsCD2 70-90%s-CD3 0%c-CD3 95%CD4 0%CD5 0%CD7 80-90%CD8 30-40%CD11b* 80-90%CD16* 80-90%CD56* 95%CD57* 50-60%CD25 95%* Commonly used NK markers,but expressed in both NK cellsand NK-like T cells

2、Discrepancy of CD3 expressionin NK cellsCD3 is a TCR-associated complexFormed by 6 chains: , , 2, 2NK cells have cytoplasmic or , but cannot assemble intact CD3 complexConventional CD3 antibody detects chain “cytoplasmic CD3”Surface CD3 (as detected by Leu4/OKT3) by flow cytometry or on frozen tissu

3、e is NEGATIVETCRLeu4, OKT3结外NK/T细胞淋巴瘤,鼻型a鼻腔、鼻咽部、鼻窦及腭部最常见,皮肤、软组织、胃肠道和睾丸亦常见。b鼻腔者表现为鼻塞、鼻衄,粘膜坏死及溃疡。皮肤病变表现为结节并多伴有溃疡。发生在肠道者常发生穿孔。c肿瘤常有噬血管性,多伴有血管破坏和坏死。 d常坏死明显,活检取材要取及非坏死瘤组织,常需多次取材才能确诊。 大多数病例为EBV(+)、CD56(+)的NK细胞表型,而少数病例具有EBV(+)、CD56(-)的细胞毒性T细胞表型。SmallMedium-sizedLargeBroad cytologic spectrumMorphologic feat

4、uresSurface squamous epithelium can show florid pseudoepitheliomatous hyperplasiaEntrapped nasal mucosal glands often show clear cell changeSkin: infiltrate often perivascular and periadnexal, but sometimes diffuse dermal; subcutis can be involvedIntestine: Ulceration and perforation commonSkinIntes

5、tineTestisMuscle结外NK/T细胞淋巴瘤的免疫表型CD2 +表面 CD3 -;胞浆 CD3 + (polyclonal CD3; PS1)CD56 +, CD57和CD16常-CD4, CD5, CD7, CD8: 常-CD43, CD45RO: 常+细胞毒颗粒 + Ki67 : 高CD25和 CD30偶尔+TCR-; CD3CD5CD56Granzyme BExtranodal NK/T cell lymphoma: GenotypeTCR genes: germline in most cases studiedEBVPresent in clonal episomal fo

6、rmNasal: 95% positive, irrespective ofethnic originExtra-nasal: 90% positive in Asians,but lower % in CaucasiansExtranodal NK/T cell lymphoma: Main problems in diagnosisBiopsies may show extensive coagulative necrosis, rendering it impossible to make a definitive diagnosis. Repeat biopsy is required

7、.Some examples comprise small cells with minimal cytologic atypia: distinction from reactive lymphoid infiltrate very difficultBEWARE:Mucosal small lymphoidcells often appear slightlylarger than small lymphocytes,and can show irregular nucleiHistologic features favoring a neoplastic processAbnormal

8、architecture:Dense expansile infiltrate with wide separation and loss of mucosal glandsTissue ulceration and necrosisEvidence of invasion:Angiocentric growthCytologic atypia:Clear cytoplasmMedium-sized; nuclear irregularities; granular chromatinReadily found mitotic figures in a small cell lesionImm

9、unohistochemical analysis:First-tier panelCD20, CD3, CD56, (Ki67)Nodular aggregates of B cells separated by T cells; few CD56+ cellsReactive lymphoidinfiltrateDense sheets of B cellsB celllymphomaDense sheets of CD3+ CD56+ cellsNK/T celllymphomaDense sheets of CD3+ CD56- cellsReactive orCD56- NK/Tly

10、mphoma orT cell lymphomaHow to confirm a suspicion ofNK/T cell lymphoma?Immunostain for CD56: large clusters or sheets of positive cells strongly support diagnosis of lymphoma Pitfall: herpes infectionIn-situ hybridization for EBER: large groups of positive cells support diagnosis of lymphomaImmunostain for Ki67: High index (80%) for a small cell-predominant lesion suggests lymphomaDiagnosis more difficult for CD56- subset:Besides EBV+, need to demonstrate cytotoxic markers谢谢

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