Fruhwirth J, Koch G, Hauser H, Gutschi S, Beham A, Kainz J
Department of Surgery, Karl Franzens University of Graz, Austria.
Eur J Surg Oncol. 1996 Feb;22(1):88-92. doi: 10.1016/s0748-7983(96)91748-5.
The present study reviews in concise form the past 12 years of our clinical experience with paragangliomas of the carotid body. Every aspect of the anatomical, histological and biological and biological behaviour of paragangliomas of the carotid body has been recorded in order to be able to define better surgical management and the clinical prognosis. In addition to the conventional histological methods of investigation we also applied immunohistochemistry and made use of electron microscopy. Eighteen tumours of the carotid body in 12 female and four male patients with a mean age of 54 years (34 to 70 years) were treated surgically. Angiography of the aortic arch and supra-aortic branches was undertaken diagnostically in every case. In three patients computer tomography and magnetic resonance imaging demonstrated spreading of the tumour up to the base of the skull and pre-operative embolization of the arteries supplying the tumour was performed to decrease tumour vascularity. In four cases (22%) resection of the internal carotid artery and its reconstruction by a saphenous vein graft was required in order to achieve the therapeutic aim of a complete extirpation of tumourous tissue and preserving the vascular system of the internal carotid artery. In three cases (16%) there was histological evidence of a metastasizing process to the local lymph nodes of the neck and, due to this criterion of malignancy, 50-60 Gy of radiation was applied to the site of the tumour after surgery. Four patients experienced a transient neurological deficit in the supply area of the hypoglossal and the recurrent nerves. In one case, the vagus nerve could not be retained. In an average follow-up of 102 months we recorded one case of local recurrence 13 months after the initial resection and radiation treatment applied to a malignant paraganglioma. All the other patients were doing well without evidence of recurrent disease.
本研究以简明的形式回顾了我们过去12年中对颈动脉体副神经节瘤的临床经验。记录了颈动脉体副神经节瘤在解剖学、组织学、生物学及生物学行为等各个方面的情况,以便能更好地确定手术治疗方法和临床预后。除了传统的组织学检查方法外,我们还应用了免疫组织化学并利用了电子显微镜。对12例女性和4例男性患者的18个颈动脉体肿瘤进行了手术治疗,患者平均年龄54岁(34至70岁)。每例均进行了主动脉弓及主动脉上部分支的血管造影检查。3例患者经计算机断层扫描和磁共振成像显示肿瘤已蔓延至颅底,术前对供应肿瘤的动脉进行了栓塞以减少肿瘤血管。4例(22%)患者为了实现完全切除肿瘤组织并保留颈内动脉血管系统的治疗目标,需要切除颈内动脉并用大隐静脉移植进行重建。3例(16%)有组织学证据表明肿瘤已转移至颈部局部淋巴结,基于这种恶性标准,术后对肿瘤部位给予了50 - 60 Gy的放疗。4例患者在舌下神经和喉返神经的供应区域出现了短暂的神经功能缺损。1例患者的迷走神经未能保留。在平均102个月的随访中,我们记录到1例恶性副神经节瘤在初次切除及放疗后13个月出现局部复发。所有其他患者情况良好,无疾病复发迹象。