嗜铬细胞瘤/副神经节瘤与Takotsubo综合征研究进展

Pheochromocytoma/Paraganglioma Associated with Takotsubo Syndrome

近年来Takotsubo综合征(TTS)在全世界范围内逐渐受到关注。嗜铬细胞瘤/副神经节瘤作为一种少见的神经内分泌肿瘤,也是此病的诱因之一。随着TTS病例报道的增多和临床研究的开展,嗜铬细胞瘤与TTS的密切关系近年来已逐渐引起学者的重视。但嗜铬细胞瘤诱发的TTS缺乏统一的诊断指征,所以该类疾病的诊断常被延误。现就嗜铬细胞瘤诱发的TTS在临床表现、电生理、解剖类型、代谢、复发率等方面与其他类型的TTS存在的差异特点进行论述。

Takotsubo syndrome(TTS)has attracted more and more worldwide attention in recent years.Pheochromocytoma/paraganglioma,as a rare neuroendocrine neoplasm,is also one of the causes of this disease.With the increase of reports of TTS cases and the development of clinical research,the close relationship between pheochromocytoma and TTS has gradually attracted attention in recent years.However,the diagnosis of pheochromocytoma-induced TTS is often delayed due to the lack of unified diagnostic indicators.The differences between pheochromocytoma-induced TTS and other types of TTS in clinical manifestations,electrophysiology,anatomical types,metabolism and recurrence rate are discussed in this article.