Borota O Casar, Scheithauer B W, Fougner S Lyngvi, Hald J K, Ramm-Pettersen J, Bollerslev J
Pathology Clinic, Rikshospitalet University Hospital, Oslo, Norway.
Clin Neuropathol. 2009 Mar-Apr;28(2):91-5. doi: 10.5414/npp28091.
Spindle cell oncocytoma (SCO) of the adenohypophysis is a recently defined pituitary tumor mimicking a non-functioning macroadenoma and composed of mitochondrion rich tumor cells, positive for S-100, vimentin, epithelial membrane antigen and galectin-3 but lacking cytokeratins, pituitary hormones, and neuroendocrine markers. Derivation from pituitary folliculostellate cells (FSCs) has been suggested based upon immunohistochemical and ultrastructural characteristics shared by SCO and FSCs. 10 cases of SCO have been reported to date; of these, 8 underwent a benign clinical course and 2 recurred. We report a case of SCO with typical histologic and immunohistochemical features in addition to marked cellular pleomorphism and nuclear atypia. It showed slow regrowth over a 30-month period of follow-up despite combined surgical and radiotherapy. Despite the benign course of most reported cases, additional experience with longer follow-up are needed to assess clinical, histopathologic, and proliferative indices and their relevance to optimal therapy for this rare pituitary tumor.
腺垂体的梭形细胞嗜酸细胞瘤(SCO)是一种最近定义的垂体肿瘤,它类似无功能大腺瘤,由富含线粒体的肿瘤细胞组成,S-100、波形蛋白、上皮膜抗原和半乳糖凝集素-3呈阳性,但缺乏细胞角蛋白、垂体激素和神经内分泌标志物。基于SCO和垂体滤泡星状细胞(FSC)共有的免疫组织化学和超微结构特征,提示其起源于垂体滤泡星状细胞。迄今为止,已报道10例SCO;其中8例临床病程呈良性,2例复发。我们报告1例SCO,除具有典型的组织学和免疫组织化学特征外,还具有明显的细胞多形性和核异型性。尽管接受了手术和放疗联合治疗,但在30个月的随访期间它仍缓慢再生长。尽管大多数报道病例的病程呈良性,但仍需要更多长期随访的经验来评估临床、组织病理学和增殖指数,以及它们与这种罕见垂体肿瘤最佳治疗方法的相关性。