Cheaito R, Tritar A, Benamer H, Saighi Bouaouina M, Masri A, Bouzid M A, Younes M, Mansour H, Jessen P
Service de cardiologie, hôpital européen de Paris, La Roseraie, 120, avenue de la République, 93300 Aubervilliers, France; Hôpital privé Jacques-Cartier, 6, avenue du Noyer-Lambert, 91300 Massy, France; Service de cardiologie, Beirut cardiac institute, airport St, Beirut, Liban.
Service de cardiologie, hôpital européen de Paris, La Roseraie, 120, avenue de la République, 93300 Aubervilliers, France.
Ann Cardiol Angeiol (Paris). 2017 Dec;66(6):411-414. doi: 10.1016/j.ancard.2017.10.013. Epub 2017 Nov 2.
The pheochromocytome is a localized tumor at the level of the medullosurrenale in 85% of the cases. The clinical presentation is very variable. Severe Heart failure presentation can be the mode of revelation in 2% of the cases. We present the case of a patient admitted for refractory cardiogenic shock correlated to pheochromocytome tumor. The difficulty of this rare clinical presentation was to confirm rapidly and in emergency this diagnosis in the same time when the patient presents a persistante and severe cardiogenic chock after finding a sub-occluded and thrombotic LAD coronary artery and which was treated by thrombectomy and coronary revascularization. The surgical treatment of this tumor is considered to be a quickly saving treatment. It allows a fast recovery of the cardiac function.
嗜铬细胞瘤在85%的病例中是肾上腺髓质水平的局限性肿瘤。临床表现差异很大。严重心力衰竭表现可在2%的病例中作为首发症状。我们报告一例因与嗜铬细胞瘤相关的难治性心源性休克入院的患者。这种罕见临床表现的难点在于,在患者发现左前降支冠状动脉次全闭塞并血栓形成且已接受血栓切除术和冠状动脉血运重建后仍出现持续性严重心源性休克的情况下,要在紧急情况下迅速确诊。该肿瘤的手术治疗被认为是一种能迅速挽救生命的治疗方法。它能使心功能快速恢复。