Mehta Christopher K, Gillespie Colin T, Lin Xiaoqi, Yeldandi Anjana, DeCamp Malcolm, Bharat Ankit
Department of Surgery, Division of Thoracic Surgery, Northwestern Memorial Hospital, Chicago, Illinois.
Department of Medicine, Division of Pulmonary & Critical Care Medicine, Northwestern Memorial Hospital, Chicago, Illinois.
Ann Thorac Surg. 2015 Aug;100(2):702-5. doi: 10.1016/j.athoracsur.2014.09.068.
Mediastinal paragangliomas are rare neural crest derived tumors that may produce symptoms of excess catecholamine production or mass effect. Paragangliomas can histologically mimic neuroendocrine tumors. Further, both can arise in similar locations. We report a patient who presented with a right upper lobe as well as middle mediastinal lesion. Preoperative biopsy as well as intraoperative frozen section of these lesions failed to distinguish between paraganlioma or neuroendocrine tumor, necessitating a right upper lobectomy and complete mediastinal lymphadenectomy. Final pathology revealed carcinoid tumorlets in the right upper lobe and a middle mediastinal paraganglioma.
纵隔副神经节瘤是一种罕见的起源于神经嵴的肿瘤,可产生儿茶酚胺分泌过多或占位效应的症状。副神经节瘤在组织学上可酷似神经内分泌肿瘤。此外,两者可发生于相似部位。我们报告一例患者,其右上叶及纵隔中部出现病变。这些病变的术前活检及术中冰冻切片均未能区分副神经节瘤或神经内分泌肿瘤,因此需要进行右上叶切除术及纵隔完全淋巴结清扫术。最终病理显示右上叶有类癌小结节,纵隔中部有副神经节瘤。