Walker W P, Landas S K, Bromley C M, Sturm M T
Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City.
Mod Pathol. 1991 Sep;4(5):661-6.
Chondroid chordomas are cartilage-rich neoplasms, most often located in the spheno-occipital region, that have a better prognosis than classic chordomas. The immunohistochemical features of 19 classic and chondroid chordomas were studied retrospectively using avidin-biotin-complex (ABC) immunoperoxidase histochemistry on formalin-fixed, paraffin-embedded tissue. Of the 19 tumors, all located in the spheno-occipital region, 5 exhibited predominantly chondroid morphologic features. The 14 classic chordomas showed the following pattern of antigen expression (percent of tumors positive): epithelial membrane antigen (EMA) 100%, AE 1/3 (a "cocktail" of monoclonal antibodies directed against low and high molecular weight epidermal cytokeratins) 100%, DP keratin (DPK) 100%, vimentin 100%, S100 86%, neuron specific enolase (NSE) 100%, carcinoembryonic antigen (CEA) 57%, and HMB-45 (an anti-melanoma-associated antibody) 57%. The five chondroid chordomas exhibited the following pattern: EMA 0%, AE 1/3 0%, DPK 0%, vimentin 100%, S100 100%, NSE 100%, CEA 0%, and HMB-45 0%. The focal, weak HMB-45 positivity (performed on the index case because of a clinical concern of metastatic melanoma) seen in 57% of the classic chordomas is a previously unreported finding. This finding suggests either that classic chordomas are capable of HMB-45 expression or that this antibody has broader reactivity than previously recognized. The lack of cytokeratin, EMA, and CEA expression by the chondroid chordomas is similar to chondrosarcomas as reported in the literature and dissimilar to the classic chordoma group. These immunohistochemical findings suggest that chondroid chordomas may more validly be classified as low grade chondrosarcomas.
软骨样脊索瘤是富含软骨的肿瘤,最常位于蝶枕区域,其预后比经典型脊索瘤更好。对19例经典型和软骨样脊索瘤的免疫组化特征进行了回顾性研究,采用抗生物素蛋白-生物素复合物(ABC)免疫过氧化物酶组织化学方法,对福尔马林固定、石蜡包埋的组织进行检测。19例肿瘤均位于蝶枕区域,其中5例主要表现为软骨样形态特征。14例经典型脊索瘤呈现出以下抗原表达模式(阳性肿瘤的百分比):上皮膜抗原(EMA)100%,AE 1/3(针对低分子量和高分子量表皮细胞角蛋白的单克隆抗体“混合物”)100%,DP角蛋白(DPK)100%,波形蛋白100%,S100 86%,神经元特异性烯醇化酶(NSE)100%,癌胚抗原(CEA)57%,以及HMB-45(一种抗黑色素瘤相关抗体)57%。5例软骨样脊索瘤呈现出以下模式:EMA 0%,AE 1/3 0%,DPK 0%,波形蛋白100%,S100 100%,NSE 100%,CEA 0%,以及HMB-45 0%。在57%的经典型脊索瘤中出现的局灶性、弱阳性HMB-45阳性(因临床怀疑转移性黑色素瘤而对索引病例进行检测)是一项此前未报道的发现。这一发现表明,要么经典型脊索瘤能够表达HMB-45,要么该抗体的反应性比之前认为的更广泛。软骨样脊索瘤缺乏细胞角蛋白、EMA和CEA表达,这与文献报道的软骨肉瘤相似,与经典型脊索瘤组不同。这些免疫组化结果表明,软骨样脊索瘤可能更合理地被归类为低级别软骨肉瘤。