Epari Sridhar, Bhatkar Rohini, Moyaidi Aliasgar, Shetty Prakash, Gupta Tejpal, Kane Subhada, Jalali Rakesh
Department of Pathology, Tata Memorial Hospital and ACTREC, Mumbai, Maharashtra, India.
Indian J Pathol Microbiol. 2014 Oct-Dec;57(4):542-8. doi: 10.4103/0377-4929.142645.
Hemangioblastomas (HBs) are rare WHO grade I neoplasms of uncertain histogenesis. Most are sporadic and association with von Hippel-Lindau disease (VHL) is uncommon.
Histomorphological and immunohistochemical evaluation of 24 cases of HBs was done.
Age range was 15-68 yrs (median: 30 yrs) with male:Female of 1.2:1 (M-13; F-11). Cerebellum was commonest location (n = 20), one each was seen in brain stem, cervical spinal cord, fourth ventricle and frontal lobe, respectively. VHL association was noted in 5 cases. Four cases were recurrent in nature of which 3 were in association with vHL. Histologically, reticular variant was the predominant subtype (n = 15), 5 were of cellular variant and 4 were mixed. Nuclear pleomorphism, nuclear cytoplasmic inclusions, cytoplasmic vacuolation were noted in the stromal cells in varying proportions. Immunohistochemical evaluation was successful in only 11 cases and of which 8 showed stromal cell positivity for alpha-inhibin. CD56 (NCAM), Nestin and synaptophysin positivity was seen in 6, 7 and 4 cases, respectively. Nestin positivity was noted in stromal cells only and no reactivity with the endothelial cells seen. S-100 protein and NSE positivity was seen in 8 and 10 cases, respectively. Glial fibrillary acidic protein (GFAP) showed two distinct patterns of immunoreactivity - scattered stromal cell positivity (n:5) and pattern of reactive astrogliosis positivity (n:10). CD44 positivity was noted in 5 cases. VEGF and EGFR positivity was seen in 5 cases each. None of the cases showed positivity for epithelial membrane antigen and no stromal cells in any of the cases showed positivity for CD34 and CD31.
HBs can occur in throughout the neuroaxis. Cerebellum is the commonest site of occurrence for HBs and uncommonly can occur in the supratentorial compartment and spinal cord. Its association with vHL is uncommon and no histological or immunohistochemical correlation was identified with the same.
血管母细胞瘤(HBs)是世界卫生组织(WHO)I级的罕见肿瘤,其组织发生尚不明确。大多数为散发性,与冯·希佩尔-林道病(VHL)相关的情况并不常见。
对24例血管母细胞瘤进行了组织形态学和免疫组织化学评估。
年龄范围为15至68岁(中位数:30岁),男女比例为1.2:1(男性13例;女性11例)小脑是最常见的发病部位(n = 20);脑干、颈髓、第四脑室和额叶各有1例。发现5例与VHL相关。4例为复发性,其中3例与VHL相关。组织学上,网状亚型是主要亚型(n = 15),5例为细胞型亚型且4例为混合型。在基质细胞中可见不同比例存在核多形性、核内胞质包涵体及胞质空泡化。免疫组织化学评估仅在11例中成功,其中8例显示基质细胞α-抑制素阳性。分别在6、7和4例中观察到CD56(神经细胞黏附分子,NCAM)、巢蛋白和突触素阳性。仅在基质细胞中观察到巢蛋白阳性,未见其与内皮细胞有反应性变化。分别在8例和10例中观察到S-100蛋白和神经元特异性烯醇化酶(NSE)阳性。胶质纤维酸性蛋白(GFAP)显示出两种不同的免疫反应模式——散在的基质细胞阳性(n:5)和反应性星形胶质细胞增生阳性模式(n:10);5例中观察到CD44阳性。各有5例观察到血管内皮生长因子(VEGF)和表皮生长因子受体(EGFR)阳性。所有病例均未显示上皮膜抗原阳性,且所有病例中的基质细胞均未显示CD34和CD31阳性。
血管母细胞瘤可发生于整个神经轴。小脑是血管母细胞瘤最常见的发病部位,罕见发生于幕上腔和脊髓。其与VHL相关的情况并不常见,且未发现与之相关的组织学或免疫组织化学关联。