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Phaeochromocytoma and Paraganglioma Excision Involving the Great Vessels

机译:嗜铬细胞瘤和副神经节瘤切除涉及大血管

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Objective/background Phaeochromocytomas and paragangliomas are vascular neuroendocrine tumours distributed between the neck and the pelvis and may be associated with catecholamine secretion. The aim of the study was to describe the complex surgical management required to excise these tumours when in close proximity to the great vessels (aorta and vena cava). Methods This was a retrospective case series. Patients included those undergoing surgical excision of a phaeochromocytoma or paraganglioma involving the great vessels. Data on clinical presentation; genetic mutations; tumour location; catecholamine/metanephrine secretion; surgical strategy; pre-, intra-, and post-operative course were collated. Results Five patients (age range 16–60 years) were identified; three had thoracic paragangliomas located under the arch of the aorta, one had an abdominal paraganglioma invading the aorta, and one had a massive phaeochromocytoma invading the inferior vena cava via the adrenal vein. Three patients had predisposing germline mutations. All patients had adrenergic blockade prior to surgery. A diverse range of complex surgical techniques were employed to excise tumours, including cardiopulmonary bypass, aortic resection, grafting and venotomy of the vena cava. Early post-operative complications were limited. Conclusions Excision of phaeochromocytomas and paragangliomas involving the great vessels is high risk surgery optimally undertaken within a multidisciplinary setting in a tertiary referral centre. Comprehensive radiological and biochemical assessment, meticulous pre-operative preparation and close intra- and post-operative monitoring are essential. Radiological imaging may be unable to resolve the tumour extent and anatomy pre-operatively and direct visualisation of the tumour may be the only way to clarify the surgical strategy. Pre-operative knowledge of the genetic predisposition may influence surgical management. Highlights ? Highly vascular tumours which may be associated with catecholamine secretion. ? Comprehensive pre- and intra-operative preparation is essential. ? Final surgical strategy often requires direct tumour visualisation. ? The surgical strategy may alter for germline associated tumours. ? Management should be delivered by experienced multidisciplinary teams.
机译:目的/背景嗜铬细胞瘤和副神经节瘤是分布在颈部和骨盆之间的血管神经内分泌肿瘤,可能与儿茶酚胺的分泌有关。该研究的目的是描述在靠近大血管(主动脉和腔静脉)时切除这些肿瘤所需的复杂手术管理。方法这是一个回顾性病例系列。患者包括那些接受手术切除的巨噬细胞吞噬性嗜铬细胞瘤或神经节瘤的患者。临床表现数据;基因突变;肿瘤位置;儿茶酚胺/肾上腺素分泌;手术策略整理术前,术中和术后过程。结果确定了5例患者(年龄16至60岁)。 3例位于主动脉弓下方的胸旁神经节瘤,1例侵犯腹主动脉的腹旁神经节瘤,1例通过肾上腺静脉侵犯下腔静脉的大量嗜铬细胞瘤。三名患者有易感种系突变。所有患者在手术前均进行了肾上腺素能阻滞。多种复杂的外科手术技术被用于切除肿瘤,包括体外循环,主动脉切除,腔静脉移植和静脉切开术。术后早期并发症有限。结论涉及大血管的嗜铬细胞瘤和副神经节瘤的切除是高风险的手术,最好在三级转诊中心的多学科环境中进行。全面的放射和生化评估,精心的术前准备以及密切的术中和术后监测至关重要。放射影像学检查可能无法解决肿瘤的范围,术前的解剖结构和肿瘤的直接可视化可能是阐明手术策略的唯一方法。遗传易感性的术前知识可能会影响手术管理。强调 ?高度血管性肿瘤,可能与儿茶酚胺分泌有关。 ?全面的术前和术中准备至关重要。 ?最终手术策略通常需要直接观察肿瘤。 ?手术策略可能会因种系相关肿瘤而改变。 ?应由经验丰富的多学科团队进行管理。

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