复发性感觉神经母细胞瘤的放射外科治疗1例

A. Tokarev, V. Rak, V. Stepanov, V. Krylov
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引用次数: 0

摘要

感觉神经母细胞瘤是一种罕见的神经外胚层肿瘤,发病率为0.4 / 100万,约占鼻窦恶性肿瘤的2-3%,无性别倾向[1,2]。ENB最早由Berger等人于1924年描述,此后约有1200例报告[3,4]。肿瘤起源于位于鼻上结构、筛板和前颅底的感觉嗅觉上皮基底干细胞[4,5]。最常见的症状是鼻塞、鼻出血、嗅觉丧失、鼻漏或流泪。由于肿瘤早期无症状表现,晚期临床表现导致颅底受累率高。因此,主要的治疗方式往往是颅面切除术,辅助外束放疗和化疗[7]。尽管联合治疗,局部复发的风险约为20-50%[4-7]。立体定向放射治疗(SRS)作为一种无创治疗方法,在ENB术后局部复发患者中,尤其是深部病变患者中,是安全有效的。在这里,我们报告了伽玛刀SRS治疗侵袭性卡迪什C期(“扩散到鼻腔和鼻副腔之外”)感觉神经母细胞瘤的经验,该瘤累及右眼眶、前颅窝和颞斜区。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiosurgical Treatment of Recurrent Esthesioneuroblastoma: Case Report
Esthesioneuroblastoma is an uncommon neuroectodermal tumor occurring with an incidence of 0.4 per 1 million and constitutes approximately 2-3% of sinonasal malignancies with no gender predilection [1,2]. ENB was first described by Berger et al. [3] in 1924 and since then approximately 1200 cases have been reported [3,4]. The tumor arises from basal stem cells of sensory olfactory epithelium locating on superior nasal structures, cribriform plate and anterior skull base [4,5]. The most common symptoms are nasal congestion and epistaxis, anosmia, rhinorrhea or lacrimation [6]. Late clinical manifestation resulting from asymptomatic behavior of the tumor on early stages leads to high rate skull base involvement. Therefore the primary treatment modality is often a craniofacial resection, adjuvant external beam radiotherapy and chemotherapy [7]. Despite combined treatment the risk of local recurrence is about 20-50% [4-7]. Appliance of stereotactic radiosurgery (SRS) as a non-invasive treatment modality can be safe and effective in group of patients with local recurrence of ENB after surgery, especially in cases of deep located lesions. Here we present our experience of Gamma Knife SRS for an aggressive Kadish stage C (‘spread beyond nasal and paranasal cavities’) esthesioneuroblastoma involving right orbit, anterior cranial fossa and sphenopetroclival region.
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