Osman Mostafa, Wild Andrew
Department of Neurosurgery, Dr. Soliman Fakeeh Hospital, Jeddah, Saudi Arabia.
Am J Case Rep. 2017 Aug 17;18:894-901. doi: 10.12659/ajcr.903702.
BACKGROUND Spindle cell oncocytoma (SCO) is a rare nonfunctioning neoplasm of the adenohypophysis, and was first described in 2002. SCO has been categorized as a separate entity by the 2007 World Health Organization (WHO) and is classified as a Grade 1 tumor of the central nervous system (CNS). Review of the literature has shown that 33 cases of SCO have been reported to date, and most of them presented with a mass effect or with panhypopituitarism. However, all reported cases have described the tendency of SCO to be hypervascular on imaging and histology. We detail the first reported case of SCO to present with acute symptoms (pituitary apoplexy) and intraventricular hemorrhage, and review the literature on SCO. CASE REPORT We report the case of 56-year-old man who presented suddenly with a severe headache and an altered level of consciousness. Brain magnetic resonance imaging (MRI) showed a suprasellar mass with hemorrhagic areas within the tumor and bleeding into the lateral ventricle with chiasmal and hypothalamic compression. The patient underwent urgent craniotomy, tumor resection and placement of an external ventricular drain (EVD). Histology and immunohistochemistry supported a diagnosis of SCO. CONCLUSIONS SCO of the adenohypophysis should be considered in patients who present suddenly with symptoms of pituitary apoplexy and intraventricular hemorrhage which may worsen the prognosis.
背景 梭形细胞嗜酸细胞瘤(SCO)是腺垂体一种罕见的无功能肿瘤,于2002年首次被描述。SCO在2007年世界卫生组织(WHO)分类中被归为一个独立实体,被列为中枢神经系统(CNS)1级肿瘤。文献回顾显示,迄今为止已报道33例SCO,其中大多数表现为占位效应或全垂体功能减退。然而,所有报道病例均描述了SCO在影像学和组织学上的高血供倾向。我们详细介绍首例表现为急性症状(垂体卒中)和脑室内出血的SCO病例,并回顾SCO的相关文献。病例报告 我们报告一名56岁男性患者,他突然出现严重头痛和意识水平改变。脑部磁共振成像(MRI)显示鞍上肿块,肿瘤内有出血区域,并向侧脑室出血,伴有视交叉和下丘脑受压。患者接受了紧急开颅手术、肿瘤切除及外置脑室引流管(EVD)置入。组织学和免疫组化支持SCO的诊断。结论 对于突然出现垂体卒中症状和脑室内出血且可能使预后恶化的患者,应考虑腺垂体SCO的可能。