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一例纵隔副神经节瘤切除术病例报告:为何如此大惊小怪?

A Case Report of Resection of a Mediastinal Paraganglioma: Why All the Fuss?

作者信息

Staunton Laura Mary, Casey Laura, Young Vincent K, Fitzmaurice Gerard J

机构信息

Department of Cardiothoracic Surgery, St. James's Hospital, Dublin, Ireland.

出版信息

J Chest Surg. 2022 Apr 5;55(2):174-176. doi: 10.5090/jcs.21.115.

Abstract

Mediastinal paragangliomas are rare tumors that have only been reported in individual cases or limited case series. Surgical resection of these tumors can be challenging, as they are highly vascular and intimately related to the great vessels. Surgery is usually performed via median sternotomy with or without cardiopulmonary bypass. We present the case of a mediastinal paraganglioma that was resected via a left-sided posterolateral thoracotomy. Histopathology revealed a completely resected 38-mm paraganglioma with a positive station 5 lymph node, indicative of locally aggressive disease. Hereditary paragangliomas are associated with malignant transformation; therefore, genetic testing is important. These tumors do not respond well to chemoradiotherapy, and consequently lifelong surveillance for early detection of recurrence is recommended.

摘要

纵隔副神经节瘤是罕见肿瘤,仅在个别病例或有限的病例系列中有报道。这些肿瘤的手术切除具有挑战性,因为它们血管丰富且与大血管关系密切。手术通常通过正中胸骨切开术进行,可在有或没有体外循环的情况下进行。我们报告一例通过左侧后外侧开胸手术切除的纵隔副神经节瘤病例。组织病理学显示一个完全切除的38毫米副神经节瘤,第5组淋巴结阳性,提示局部侵袭性疾病。遗传性副神经节瘤与恶性转化有关;因此,基因检测很重要。这些肿瘤对放化疗反应不佳,因此建议进行终身监测以早期发现复发。

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