Department of Thoracic Surgery, Kaplan Medical Center, Rehovot and The Hebrew University School of Medicine, Jerusalem, Israel; Institute of Oncology, Tel Aviv Sourasky Medical Center and The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Surgery, Kaplan Medical Center, Rehovot and The Hebrew University School of Medicine, Jerusalem, Israel.
Ann Thorac Surg. 2019 Dec;108(6):e349-e351. doi: 10.1016/j.athoracsur.2019.03.106. Epub 2019 May 8.
Paragangliomas are rare neuroendocrine tumors derived from extraadrenal autonomic paraganglia, which may secrete catecholamines. They are potentially metastatic and require very long-term follow-up. Esophageal paragangliomas are extremely rare and present a diagnostic challenge. Lack of clinical suspicion and unrecognized catecholamine hypersecretion may lead to hemodynamic instabilities during surgery. Two patients with esophageal paragangliomas were previously reported. We report a 39-year-old man with a giant high-risk esophageal paraganglioma who underwent a hybrid minimally invasive 3-hole esophagectomy.
副神经节瘤是一种罕见的神经内分泌肿瘤,来源于肾上腺外自主副神经节,可能分泌儿茶酚胺。它们具有潜在的转移性,需要进行非常长期的随访。食管副神经节瘤极为罕见,诊断具有挑战性。缺乏临床怀疑和未被识别的儿茶酚胺分泌过多可能导致手术期间血流动力学不稳定。此前曾报道过两例食管副神经节瘤患者。我们报告了一例 39 岁男性患有巨大高危食管副神经节瘤,行杂交微创 3 孔食管切除术。