Jianu Dragoş Cătălin, Jianu Silviana Nina, Motoc Andrei Gheorghe Marius, Dan Traian Flavius, Poenaru Mărioara, Tăban Sorina, CreŢu Octavian Marius
Department of Anatomy and Embryology, "Victor Babes" University of Medicine and Pharmacy, Timisoara, Romania;
Rom J Morphol Embryol. 2016;57(2 Suppl):853-859.
Carotid body paragangliomas (CBPGLs) are a rare neoplasms of the neuroendocrine system that affect the carotid glomus. The aim of this study is to improve their management in our Departments. This retrospective analysis reports family history, clinical presentation, imaging diagnostics, Shamblin classification, surgical treatment, complications, and the outcome of seven patients with CBPGLs. All lesions were represented by a painless cervical mass, with no functional or bilateral neck tumors. One patient had two different localizations (the second one was a glomus tumor of the right prelachrymal sac), and a family history for CBPGL. All neck tumors were diagnosed during duplex ultrasound corroborated by magnetic resonance imaging (MRI), and by magnetic resonance angiography (MR-A). They presented a diameter between 3 and 5 cm (MRI). Complete subadventitial resection of the tumor was performed in all patients, with no preoperative embolization in any of the cases. The CBPGLs were confirmed on histopathology and immunohistochemistry. Lymph node metastasis was not found in any of the cases. Mortality and perioperative stroke rates were null. Transitory cranial nerve deficit occurred in one case without permanent palsy. After a follow-up of three years in each patient, there were no signs of tumor recurrence in any of the cases. Relatively early diagnosis of CBPGL was possible in our seven patients using multidisciplinary management. Preoperative planning of the surgical procedure by integrated diagnostic imaging was essential in our study to operate only Shamblin group II tumors, minimizing the known risk of complications associated with large CBPGL (group III).
颈动脉体副神经节瘤(CBPGLs)是一种影响颈动脉小球的神经内分泌系统罕见肿瘤。本研究的目的是改善我们科室对其的管理。这项回顾性分析报告了7例CBPGLs患者的家族史、临床表现、影像学诊断、Shamblin分类、手术治疗、并发症及预后。所有病变均表现为无痛性颈部肿块,无功能性或双侧颈部肿瘤。1例患者有两个不同的病变部位(第二个是右泪囊前的小球瘤),且有CBPGL家族史。所有颈部肿瘤均在经磁共振成像(MRI)和磁共振血管造影(MR - A)证实的双功超声检查中被诊断出来。它们在MRI上显示直径在3至5厘米之间。所有患者均进行了肿瘤的完全外膜下切除,所有病例均未进行术前栓塞。CBPGLs经组织病理学和免疫组织化学确诊。所有病例均未发现淋巴结转移。死亡率和围手术期卒中发生率为零。1例出现短暂性颅神经缺损,但无永久性麻痹。在对每位患者进行三年随访后,所有病例均无肿瘤复发迹象。在我们的7例患者中,采用多学科管理能够相对早期诊断CBPGL。在我们的研究中,通过综合诊断成像进行手术的术前规划对于仅处理Shamblin II组肿瘤至关重要,从而将与大型CBPGL(III组)相关的已知并发症风险降至最低。