血管中心性胶质瘤的分子免疫组织化学特征。

Journal of epilepsy research Pub Date : 2020-12-31 eCollection Date: 2020-12-01 DOI:10.14581/jer.20013
Lanisha D Fuller, Richard A Prayson
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引用次数: 2

摘要

背景和目的:血管中心性胶质瘤是一种罕见的世界卫生组织一级肿瘤,主要见于儿童和年轻人,通常表现为癫痫发作。组织学上表现为浸润性胶质瘤和室管膜瘤。方法:我们检查了分子免疫组织化学标记,可以帮助区分这种实体,从其鉴别诊断考虑。结果:我们回顾性回顾了血管中心性胶质瘤的临床病理特征,并对福尔马林固定石蜡包埋组织进行了异柠檬酸脱氢酶1 (IDH-1) (R132H)、p53、ATRX、BRAF V600E、Ki-67和H3 K27M的免疫组化染色。共发现7例,包括6例切除标本和1例活检。所有病例均保留ATRX染色。没有证据表明有IDH-1 (R132H)、H3 K27M或BRAF V600E抗体染色。5例肿瘤未见p53抗体染色,2例阳性低于5%。Ki-67指标5例小于1%,1例小于4-5%,1例小于9-10%。结论:ATRX、p53、IDH-1 (R132H)、BRAF V600E、H3 K27M的免疫组化标记物呈野生型染色,可能有助于避免形态学与其他低级别胶质瘤相似的病例的误诊。Ki-67标记指数在大多数肿瘤中较低。
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Molecular Immunohistochemical Profile of Angiocentric Glioma.

Background and purpose: Angiocentric glioma is a rare, World Health Organization grade I tumor that is seen predominantly in children and young adults and typically presents with seizures. Histologically, it shows features of both infiltrating glioma and ependymoma.

Methods: We examined molecular immunohistochemical markers which could help in distinguishing this entity from its differential diagnostic considerations.

Results: We retrospectively reviewed the clinicopathologic features of angiocentric gliomas and performed immunohistochemical staining for isocitrate dehydrogenase 1 (IDH-1) (R132H), p53, ATRX, BRAF V600E, Ki-67, and H3 K27M on formalin-fixed, paraffin-embedded tissue. Seven cases in total were found and included six excisional specimens and one biopsy. ATRX staining was retained in all cases. There was no evidence of staining with antibodies to IDH-1 (R132H), H3 K27M, or BRAF V600E. Five tumors showed no staining with antibody to p53 and two tumors showed less than 5% positivity. Ki-67 indices were less than 1% in five tumors, 4-5% in one tumor, and 9-10% in one tumor.

Conclusions: In conclusion, the immunohistochemical markers for ATRX, p53, IDH-1 (R132H), BRAF V600E, H3 K27M show wild-type staining, potentially aiding in avoiding misdiagnoses in cases morphologically similar to other low-grade gliomas. Ki-67 labeling indices are low in most tumors.

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