首页> 外文期刊>Pathology International >SHP-1 expression in primary central nervous system B-cell lymphomas in immunocompetent patients reflects maturation stage of normal B cell counterparts.
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SHP-1 expression in primary central nervous system B-cell lymphomas in immunocompetent patients reflects maturation stage of normal B cell counterparts.

机译:SHP-1在免疫功能正常的原发性中枢神经系统B细胞淋巴瘤中的表达反映了正常B细胞​​对应物的成熟阶段。

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摘要

SHP-1 is an important negative regulator involved in signaling through receptors for cytokine/growth factors, and differential patterns of SHP-1 expression in several types of B-cell lymphomas closely resemble the patterns seen in their normal B cell counterparts. In an effort to elucidate the origin of primary central nervous system lymphomas (PCNSL), the present study assessed 32 cases of PCNSL. Tumors were subclassified according to WHO classification and were evaluated by immunohistochemistry for expression of antigens associated with germinal center (GC) (CD10, Bcl-6) and non-GC stages (SHP-1, CD138). Twenty-nine cases showed diffuse large-cell centroblastic morphology, whereas three cases showed diffuse large-cell immunoblastic morphology. The immunophenotypes of PCNSL were as follows: SHP-1+/Bcl-6-/CD10-/CD138- (12 of 32 cases); SHP-1+/Bcl-6+/CD10-/CD138- (15 of 32 cases); SHP-1+/Bcl-6+/CD10+/CD138- (two of 32 cases); SHP-1+/Bcl-6-/CD10+/CD138- (one of 32 cases); and SHP-1-/Bcl-6-/CD10-/CD138- (two of 32 cases). These results indicate that PCNSL might be distinct lymphomas that originate from a late germinal center to an early postgerminal center.
机译:SHP-1是一种重要的负调节剂,参与通过细胞因子/生长因子受体的信号传导,并且在几种类型的B细胞淋巴瘤中SHP-1表达的差异模式与在其正常B细胞​​对应物中所见的模式非常相似。为了阐明原发性中枢神经系统淋巴瘤(PCNSL)的起源,本研究评估了32例PCNSL。根据WHO分类对肿瘤进行亚分类,并通过免疫组织化学评估与生发中心(GC)(CD10,Bcl-6)和非GC分期(SHP-1,CD138)相关的抗原的表达。 29例表现出弥散性大细胞中心粒形态,而3例表现出弥散性大细胞免疫母细胞形态。 PCNSL的免疫表型如下:SHP-1 + / Bcl-6- / CD10- / CD138-(32例中的12例)。 SHP-1 + / Bcl-6 + / CD10- / CD138-(32例中的15例); SHP-1 + / Bcl-6 + / CD10 + / CD138-(32例中的2例); SHP-1 + / Bcl-6- / CD10 + / CD138-(32例)和SHP-1- / Bcl-6- / CD10- / CD138-(32例中的2例)。这些结果表明PCNSL可能是不同的淋巴瘤,起源于生发后期至生殖后早期。

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