Kinjo Takanori, Oida Takeshi, Yoneda Suguru, Takezawa Kentaro, Nomura Hironori, Tei Norihide, Takada Shingo, Matsumiya Kiyomi
The Department of Urology, Osaka Police Hospital.
Hinyokika Kiyo. 2013 Dec;59(12):775-9.
A 46-year-old man had sudden onset of severe left hypochondrial pain and went into shock following hospitalization. Computed tomography, echocardiography, and endocrinological tests revealed spontaneous rupture of a pheochromocytoma associated with catecholamine cardiomyopathy. After he underwent conservative management with fluid replacement, his blood pressure stabilized and cardiac function improved. Twenty-two days later, he was referred to our hospital. After admission, as his circulatory dynamics was stable, we performed elective laparoscopic left adrenalectomy. He was discharged on the tenth postoperative day. Spontaneous rupture of a pheochromocytoma is very rare : laparoscopic surgery for this condition has been reported only on 2 previous occasions worldwide.
一名46岁男性突然出现严重的左季肋部疼痛,住院后陷入休克。计算机断层扫描、超声心动图和内分泌检查显示,嗜铬细胞瘤自发破裂并伴有儿茶酚胺心肌病。在接受补液保守治疗后,他的血压稳定,心脏功能改善。22天后,他被转诊至我院。入院后,由于其循环动力学稳定,我们为他进行了择期腹腔镜左肾上腺切除术。他于术后第十天出院。嗜铬细胞瘤自发破裂非常罕见:全球此前仅报道过2例针对这种情况的腹腔镜手术。