Chejfec G, Candel A, Jansson D S, Warren W H, Koukoulis G K, Gould J E, Manderino G L, Gooch G T, Gould V E
Department of Pathology, Hines VA Hospital-Loyola University School of Medicine, Maywood, Illinois.
Ultrastruct Pathol. 1991 Mar-Apr;15(2):131-8. doi: 10.3109/01913129109016231.
Giant cell carcinoma of the lung (GCCL) is an uncommon and extremely aggressive variant of lung cancer. Characteristic microscopic findings include marked pleomorphism, aggregates of mononucleated or multinucleated giant cells (or both), a general lack of architectural cohesiveness, extensive necrosis, and endocytosis by the giant cells. Although the epithelial character of GCCL has been confirmed by a number of studies, controversy persists as to whether it represents a variant of poorly differentiated adenocarcinoma or of squamous carcinoma. Histochemical studies for mucosubstances have yielded variable and conflicting results. This report describes conventionally fixed and processed samples from 10 cases of GCCL studied with a panel of monoclonal antibodies (Mabs) recognizing different cytokeratin polypeptides (AE1, AE3, AE1/AE3 cocktail, and CAM 5.2), vimentin, and Mab A-80, the last of which binds to a mucinous glycoprotein associated with exocrine differentiation. All 10 cases of GCCL reacted with all cytokeratin Mabs; the extent and intensity of the reaction varied notably. All cases stained strongly and diffusely with Mab AE1 and AE1/AE3, the reaction was less extensive and weaker with CAM 5.2. Significantly, 2 cases reacted focally with Mab AE3. Nine cases reacted extensively and intensely with the vimentin Mab, often showing prominent paranuclear globular profiles. All cases reacted with Mab A-80; the reaction was often strong, but the extent was variable. Findings indicate that all GCCL are indeed cytokeratin positive but that most express polypeptides toward the low-molecular weight end of the spectrum; a small subset also expresses heavier polypeptides.(ABSTRACT TRUNCATED AT 250 WORDS)
肺巨细胞癌(GCCL)是一种罕见且极具侵袭性的肺癌变体。特征性的显微镜下表现包括显著的多形性、单核或多核巨细胞聚集体(或两者皆有)、普遍缺乏结构连贯性、广泛坏死以及巨细胞的内吞作用。尽管多项研究已证实GCCL的上皮特征,但对于它是低分化腺癌的变体还是鳞状细胞癌的变体仍存在争议。针对黏液物质的组织化学研究结果不一且相互矛盾。本报告描述了对10例GCCL常规固定和处理的样本,使用一组识别不同细胞角蛋白多肽(AE1、AE3、AE1/AE3混合抗体和CAM 5.2)、波形蛋白以及Mab A - 80(最后一种与外分泌分化相关的黏液糖蛋白结合)的单克隆抗体进行研究。所有10例GCCL均与所有细胞角蛋白单克隆抗体发生反应;反应的程度和强度差异显著。所有病例与Mab AE1和AE1/AE3均呈强而弥漫性染色,与CAM 5.2的反应范围较小且较弱。值得注意的是,2例与Mab AE3呈局灶性反应。9例与波形蛋白单克隆抗体呈广泛而强烈的反应,常显示明显的核旁球状轮廓。所有病例均与Mab A - 80发生反应;反应通常较强,但范围不一。研究结果表明,所有GCCL确实均为细胞角蛋白阳性,但大多数表达的是低分子量谱段的多肽;一小部分也表达分子量更大的多肽。(摘要截选至250词)