{"title":"Ganglion cell maturation in peripheral neuroblastic tumours of children.","authors":"Harvey B Sarnat, Weiming Yu","doi":"10.5414/NP301450","DOIUrl":null,"url":null,"abstract":"<p><p>Peripheral neuroblastic tumours of neural crest origin are the most frequent solid neoplasms outside the CNS in children. Neuroblastoma/ganglioneuroblastoma/ganglioneuroma have a natural evolution of histological differentiation over time. Together with mitosis-karyorrhexis index and patient age (International Neuroblastoma Pathology Classification criteria), ganglion cell maturation determines grading and prognosis. Maturation presently is usually assessed only histologically. Immunocytochemical tissue markers defining neuroblast maturation in fetal CNS were here applied to peripheral neuroblastic tumours arising in the adrenal medulla or sympathetic chain. Paraffin sections of resected tumours of 4 toddlers were examined using antibodies demonstrating neuronal identity and maturation: MAP2; synaptophysin; chromogranin-A; NeuN; keratan sulfate (KS); glutamate receptor antibody (GluR2). Synaptophysin, normally a late marker of neuroblast differentiation, was the earliest expressed in neuroblastoma. Others include: Ki67; S-100β protein; vimentin; nestin; α-B-crystallin; neuroblastoma marker PHOX2B. Various degrees of ganglion cell maturation were demonstrated by MAP2, chromogranin, synaptophysin, KS, and GluR2; NeuN was uniformly negative, consistent with sympathetic neurons. KS was sparsely distributed within the tumours in interstitial tissue, within processes of some non-neuronal cells, and adherent to somata and proximal neuritic trunks. Neoplastic ganglion cells with multiple nuclei matured similar to mono-nuclear forms. PHOX2B did not distinguish maturational stages. S-100β protein and α-B-crystallin labeled Schwann cells, especially Schwannian ganglioneuroma. Immunocytochemical markers of neuroblast maturation in fetal brain also are useful in peripheral neuroblastic tumours, providing greater precision than histology alone. The most practical are MAP2, chromogranin-A, and synaptophysin. Prognosis and choice of treatment including chemotherapy might be influenced.</p>","PeriodicalId":55251,"journal":{"name":"Clinical Neuropathology","volume":"41 3","pages":"101-113"},"PeriodicalIF":0.8000,"publicationDate":"2022-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Neuropathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5414/NP301450","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 2
Abstract
Peripheral neuroblastic tumours of neural crest origin are the most frequent solid neoplasms outside the CNS in children. Neuroblastoma/ganglioneuroblastoma/ganglioneuroma have a natural evolution of histological differentiation over time. Together with mitosis-karyorrhexis index and patient age (International Neuroblastoma Pathology Classification criteria), ganglion cell maturation determines grading and prognosis. Maturation presently is usually assessed only histologically. Immunocytochemical tissue markers defining neuroblast maturation in fetal CNS were here applied to peripheral neuroblastic tumours arising in the adrenal medulla or sympathetic chain. Paraffin sections of resected tumours of 4 toddlers were examined using antibodies demonstrating neuronal identity and maturation: MAP2; synaptophysin; chromogranin-A; NeuN; keratan sulfate (KS); glutamate receptor antibody (GluR2). Synaptophysin, normally a late marker of neuroblast differentiation, was the earliest expressed in neuroblastoma. Others include: Ki67; S-100β protein; vimentin; nestin; α-B-crystallin; neuroblastoma marker PHOX2B. Various degrees of ganglion cell maturation were demonstrated by MAP2, chromogranin, synaptophysin, KS, and GluR2; NeuN was uniformly negative, consistent with sympathetic neurons. KS was sparsely distributed within the tumours in interstitial tissue, within processes of some non-neuronal cells, and adherent to somata and proximal neuritic trunks. Neoplastic ganglion cells with multiple nuclei matured similar to mono-nuclear forms. PHOX2B did not distinguish maturational stages. S-100β protein and α-B-crystallin labeled Schwann cells, especially Schwannian ganglioneuroma. Immunocytochemical markers of neuroblast maturation in fetal brain also are useful in peripheral neuroblastic tumours, providing greater precision than histology alone. The most practical are MAP2, chromogranin-A, and synaptophysin. Prognosis and choice of treatment including chemotherapy might be influenced.
神经嵴起源的周围神经母细胞肿瘤是儿童中神经系统外最常见的实体肿瘤。神经母细胞瘤/神经节神经母细胞瘤/神经节神经瘤随着时间的推移具有组织学分化的自然进化。与有丝分裂-核裂指数和患者年龄(国际神经母细胞瘤病理分类标准)一起,神经节细胞成熟度决定了分级和预后。目前的成熟度通常仅用组织学来评估。定义胎儿中枢神经系统神经母细胞成熟的免疫细胞化学组织标记物被应用于肾上腺髓质或交感神经链中产生的周围神经母细胞肿瘤。4例幼儿切除肿瘤的石蜡切片使用显示神经元身份和成熟的抗体进行检查:MAP2;synaptophysin;chromogranin-A;NeuN;硫酸角蛋白(KS);谷氨酸受体抗体(GluR2)。突触素,通常是神经母细胞分化的晚期标志,在神经母细胞瘤中最早表达。其他包括:Ki67;s - 100β蛋白;波形蛋白;巢蛋白;α-B-crystallin;神经母细胞瘤标志物PHOX2B。MAP2、嗜铬粒蛋白、突触素、KS和GluR2显示了不同程度的神经节细胞成熟;NeuN均为阴性,与交感神经元一致。KS稀疏分布于肿瘤间质组织内、部分非神经元细胞突内、附着于躯体和近端神经鞘干上。具有多核的肿瘤神经节细胞成熟时类似于单核细胞。PHOX2B不区分成熟阶段。S-100β蛋白和α- b -晶体蛋白标记的雪旺细胞,尤其是雪旺神经节神经瘤。胎儿脑神经母细胞成熟的免疫细胞化学标记物在周围神经母细胞肿瘤中也很有用,提供比单独组织学更高的准确性。最实用的是MAP2、嗜铬粒蛋白a和突触素。预后和包括化疗在内的治疗选择可能会受到影响。
期刊介绍:
Clinical Neuropathology appears bi-monthly and publishes reviews and editorials, original papers, short communications and reports on recent advances in the entire field of clinical neuropathology. Papers on experimental neuropathologic subjects are accepted if they bear a close relationship to human diseases. Correspondence (letters to the editors) and current information including book announcements will also be published.