Department of Pathology, G B Pant Institute of Postgraduate Medical Education and Research, New Delhi, India.
Department of Neurosurgery, G B Pant Institute of Postgraduate Medical Education and Research, New Delhi, India.
Neurol India. 2018 Sep-Oct;66(5):1413-1418. doi: 10.4103/0028-3886.241353.
Spindle cell oncocytoma (SCO) is a newly described rare entity simulating clinicoradiological features of a nonfunctional pituitary adenoma and is corresponding to the category of World Health Organization grade I tumor. However, because of the reported incidence of recurrence and invasive presentation in some cases, its categorization as a low grade tumor is questionable. Earlier, it was thought to arise from the folliculostellate cells of adenohypophysis. Recently, few reports have described expression of thyroid transcription factor-1 [TTF-1], which is a specific marker for pituicytes of neurohypophysis, suggesting this tumor to be a variant of pituicytoma. We describe a case of SCO in a 28-year-old young female patient with TTF-1 immunopositivity, and ultra-structurally showing abundant mitochondria along with few neurosecretory granules.
纺锤形细胞嗜酸细胞瘤(SCO)是一种新描述的罕见实体,其临床和影像学特征类似于无功能垂体腺瘤,对应于世界卫生组织(WHO)I 级肿瘤类别。然而,由于一些病例中复发和侵袭性表现的报道,其作为低级别肿瘤的分类存在疑问。早期,它被认为起源于腺垂体的滤泡星形细胞。最近,有少数报道描述了甲状腺转录因子-1(TTF-1)的表达,TTF-1 是神经垂体垂体细胞的特异性标志物,提示该肿瘤是垂体细胞瘤的一种变体。我们描述了一例 28 岁年轻女性患者的 SCO,该患者 TTF-1 免疫阳性,超微结构显示大量线粒体,伴有少量神经分泌颗粒。