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复发性家族性恶性颈动脉体瘤伴淋巴结转移:病例报告及家族性颈动脉体瘤的诊断与治疗综述

Recurrent familial malignant carotid body tumour presenting with lymph node metastasis: case report, and review of diagnosis and management of familial carotid body tumours.

作者信息

Hall T C, Renwick P, Stafford N D

机构信息

Department of ENT, Castle Hill Hospital, Cottingham, UK.

出版信息

J Laryngol Otol. 2010 Dec;124(12):1344-6. doi: 10.1017/S0022215110001489. Epub 2010 Jun 24.

Abstract

OBJECTIVE

We report the case of a recurrent familial malignant carotid body tumour presenting with metastasis to local ipsilateral lymph nodes; the rarity of both recurrence combined with nodal spread is emphasised in this article.

METHOD

We present a case report, and a review of the world literature concerning the diagnosis and management of carotid body tumours in the familial setting.

CASE REPORT

A woman with a family history of succinate dehydrogenase complex subunit B gene mutation presented with right vocal fold palsy. A causative carotid body tumour was excised. Fifteen years later, the patient developed a right-sided swelling in the jugulo-digastric region, together with shooting pains towards her right ear. Imaging revealed right posterior triangle lymphadenopathy. Fine needle aspiration cytology of the node was equivocal. Computed tomography of her neck revealed, in addition, a mass within the right side of the larynx. Excision biopsy of the lymph node demonstrated metastatic paraganglioma. A carotid angiogram revealed a right-sided carotid body tumour. This was embolised prior to neck exploration and excision of the carotid body tumour with en bloc resection of adjacent nodes. Histological analysis confirmed the presence of lymph nodes containing metastatic paraganglioma.

CONCLUSION

This case report demonstrates the need for extra vigilance to enable early disease detection in the familial setting of carotid body tumour, in order to reduce the surgical morbidity associated with disease progression. In addition, our report highlights the atypical aspects of presentation in the familial setting, together with the difficulty and lack of standardisation regarding monitoring of the disease.

摘要

目的

我们报告一例复发性家族性恶性颈动脉体瘤伴同侧局部淋巴结转移的病例;本文强调了复发与淋巴结转移同时出现的罕见性。

方法

我们呈现一例病例报告,并对有关家族性颈动脉体瘤诊断和管理的世界文献进行综述。

病例报告

一名有琥珀酸脱氢酶复合物亚基B基因突变家族史的女性出现右侧声带麻痹。切除了病因性颈动脉体瘤。15年后,患者在颈静脉二腹肌区域出现右侧肿胀,并伴有向右耳的放射性疼痛。影像学检查显示右后三角淋巴结病。对该淋巴结进行细针穿刺细胞学检查结果不明确。她颈部的计算机断层扫描还显示右侧喉内有一个肿块。淋巴结切除活检显示为转移性副神经节瘤。颈动脉血管造影显示右侧颈动脉体瘤。在颈部探查和切除颈动脉体瘤并整块切除相邻淋巴结之前,对其进行了栓塞。组织学分析证实存在含有转移性副神经节瘤的淋巴结。

结论

本病例报告表明,在家族性颈动脉体瘤患者中需要格外警惕,以便早期发现疾病,从而降低与疾病进展相关的手术发病率。此外,我们的报告突出了家族性病例表现的非典型方面,以及疾病监测的困难和缺乏标准化。

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