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神经节神经瘤:手术与否

Ganglioneuroma: to operate or not to operate.

作者信息

Sánchez-Galán Alba, Barrena Saturnino, Vilanova-Sánchez Alejandra, Martín Sara Hernández A, Lopez-Fernandez Sergio, García Purificación, Lopez-Santamaria Manuel, Martínez Leopoldo, Tovar Juan A

机构信息

Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain.

Department of Pediatric Oncology, Hospital Universitario La Paz, Madrid, Spain.

出版信息

Eur J Pediatr Surg. 2014 Feb;24(1):25-30. doi: 10.1055/s-0033-1358790. Epub 2013 Dec 10.

Abstract

INTRODUCTION

Ganglioneuroma (GN) is a benign, differentiated variety of neurogenic tumor. It is often asymptomatic and may be diagnosed by serendipity. Surgical removal is the treatment of choice. However, it has been suggested that postoperative complications and sequelae might outweigh the benefits of this approach. The purpose of the present study was to examine these issues in a large experience of neural tumors.

METHODS

Patients treated between 1992 and 2012 were retrospectively reviewed. Modern imaging, measurement of catecholamine metabolite excretion and metaiodobenzylguanidine were used for workup. Surgical treatment aimed at complete resection. Complications and sequelae were recorded. Literature was searched for regrowth or malignant transformation of GN.

RESULTS

Of 227 patients with neural tumors, 24 were GN patients (12 abdominal, 11 thoracic and 1 cervical with 8 dumbbell extensions). Six children were symptomatic (three with abdominal pain and mass, one with stridor or dysphonia, and one each with anisocoria and opsomyoclonus). However, 18 (75%) were asymptomatic and the diagnosis was incidental. Several tumors were large and involved more than one body space. There were no neurologic symptoms in eight cases with dumbbell extension. Complete resection was achieved in 20 children (83%) whereas gross residual was left in four. Postoperative complications were: Horner syndrome (3 patients), mild scoliosis (1 patient), adhesive bowel obstruction (1 patient) and acute urinary retention (1 patient). There was no evidence of either regrowth or malignant behavior in residual masses left in place after follow-up of 84 (1-194) months.

CONCLUSIONS

There were a limited number of general minor complications in this series that did not include cases of regrowth or malignant transformation. However, these unfavorable events were occasionally reported in the literature. Since diagnosis of GN cannot be ascertained before removal of the mass, this should remain the aim of the treatment, although limiting the chances of complications to a minimum even if incomplete resection is the price to pay. Nonoperative attitudes should not be recommended in all cases, but they are certainly justified in some.

摘要

引言

神经节细胞瘤(GN)是一种良性、分化型神经源性肿瘤。它通常无症状,可能偶然被诊断出来。手术切除是首选的治疗方法。然而,有人认为术后并发症和后遗症可能超过这种治疗方法的益处。本研究的目的是在大量神经肿瘤病例中探讨这些问题。

方法

对1992年至2012年期间接受治疗的患者进行回顾性分析。采用现代影像学检查、儿茶酚胺代谢产物排泄量测定和间碘苄胍检查进行诊断评估。手术治疗旨在完全切除肿瘤。记录并发症和后遗症情况。检索文献以了解神经节细胞瘤的复发或恶变情况。

结果

在227例神经肿瘤患者中,24例为神经节细胞瘤患者(12例位于腹部,11例位于胸部,1例位于颈部,其中8例有哑铃状延伸)。6例儿童有症状(3例有腹痛和肿块,1例有声嘶或发音障碍,1例有瞳孔不等大,1例有肌阵挛性斜视)。然而,18例(75%)无症状,诊断为偶然发现。几个肿瘤体积较大,累及多个身体部位。8例有哑铃状延伸的病例无神经症状。20例儿童(83%)实现了完全切除,4例有肉眼残留。术后并发症包括:霍纳综合征(3例患者)、轻度脊柱侧弯(1例患者)、粘连性肠梗阻(1例患者)和急性尿潴留(1例患者)。在随访84(1 - 194)个月后,未发现残留肿块有复发或恶变迹象。

结论

本系列中一般轻微并发症数量有限,未出现复发或恶变病例。然而,文献中偶尔也有这些不良事件的报道。由于在切除肿块前无法确诊神经节细胞瘤,尽管可能需要以不完全切除为代价将并发症几率降至最低,但手术切除仍应是治疗目标。并非所有病例都应推荐非手术治疗,但在某些情况下确实有其合理性。

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