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作 者:王健伟 王超 WANG Jian-wei;WANG Chao(Zun Yi Medical University,Zunyi 563000,China)
机构地区:[1]遵义医科大学,563000
出 处:《中国实用医药》2023年第6期144-147,共4页China Practical Medicine
摘 要:神经内分泌瘤是一种起源于肽能神经元和神经内分泌细胞、能产生生物活性胺和(或)多肽激素的异质性肿瘤,可发生于全身多种器官和组织。本文报告1例68岁女性患者,因“左眼肿胀并伴视物缺损”就诊,术前影像学诊断前颅窝嗅神经母细胞瘤可能,术后病理诊断为左侧前颅窝神经内分泌肿瘤G2期。术后因自身原因未进行放化疗,6个月后复查头颅磁共振成像(MRI)示无肿瘤复发迹象。Neuroendocrine tumors are heterogeneous tumors originating from peptidergic neurons and neuroendocrine cells that produce bioactive amines and/or peptide hormones and can occur in a variety of organs and tissues throughout the body.This article reports a case of a 68-year-old female patient who presented with"swelling of the left eye with visual deficit",and diagnosed with a possible anterior cranial fossa olfactory neuroblastoma on preoperative imaging and a stage G2 anterior cranial fossa neuroendocrine tumor on postoperative pathology.No radiotherapy or chemotherapy is performed for self-related reasons after surgery,and the brain magnetic resonance imaging(MRI)showed no sign of tumor recurrence after 6 months.
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