Successful Management of Infective Endocarditis Complicated by Pheochromocytoma: A Case Report.

IF 1.3 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2025-03-08 eCollection Date: 2025-03-01 DOI:10.7759/cureus.80269
Koki Ikemoto, Akiyuki Takahashi, Kazunari Ohkawa, Keisuke Shuntoh, Katsuhiko Oka
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Abstract

Pheochromocytomas present with paroxysmal hypertension due to a sudden release of catecholamines stimulated by radiological contrast media, surgery, or anesthetic agents. This often complicates the maintenance of patient hemodynamics during surgery. A 55-year-old man with a high fever was admitted to a hospital. Laboratory blood tests revealed elevated white blood cell and C-reactive protein levels. Transthoracic and transesophageal echocardiography revealed moderate aortic regurgitation, along with aortic valve vegetation. Magnetic resonance imaging revealed multiple cerebral embolisms, whereas computed tomography showed a left adrenal incidentaloma. Further examinations showed high levels of plasma-free metanephrine, adrenaline, and noradrenaline in the blood and metanephrines in the urine. 123I-metaiodobenzylguanidine scintigraphy revealed ligand accumulation in the tumor at 6 and 24 h after injection. Based on these results, the diagnosis of pheochromocytoma was confirmed. Doxazosin was promptly administered, and its dosage was escalated. Despite ongoing antimicrobial therapy, transesophageal echocardiography did not reveal any reduction in the size of the vegetation. Hence, the patient underwent surgical treatment. A laparoscopic left adrenalectomy was initially performed. The patient's blood pressure increased with insufflation and manipulation around the tumor but dropped immediately after the adrenal tumor was resected. Following the adrenalectomy, a cardiopulmonary bypass was established. The bicuspid aortic valve leaflets along with the vegetation were completely resected. Subsequently, a mechanical aortic valve was implanted. Inotropic agents were completely weaned off within two days after surgery. A pathological examination confirmed the adrenal incidentaloma to be pheochromocytoma. One-stage surgery with adrenalectomy before cardiac surgery using cardiopulmonary bypass may be an effective strategy for patients with pheochromocytomas diagnosed with infective endocarditis. In addition, it can reduce the risk of complications with pheochromocytoma by managing the patient's systemic condition as much as possible before cardiac surgery.

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嗜铬细胞瘤并发感染性心内膜炎的成功治疗:病例报告。
由于放射造影剂、手术或麻醉剂刺激儿茶酚胺的突然释放,嗜铬细胞瘤表现为阵发性高血压。这往往使手术期间患者血流动力学的维持复杂化。一名55岁男子因发高烧被送进医院。实验室血液检查显示白细胞和c反应蛋白水平升高。经胸和经食管超声心动图显示中度主动脉反流,并伴有主动脉瓣植被。磁共振成像显示多发性脑栓塞,而计算机断层扫描显示左侧肾上腺偶发瘤。进一步的检查显示血浆中无肾上腺素、肾上腺素和去甲肾上腺素含量高,尿液中有肾上腺素。注射后6和24小时,123i -甲氧苄基胍荧光显像显示肿瘤内的配体积累。根据这些结果,确诊为嗜铬细胞瘤。立即给予多沙唑嗪,并增加剂量。尽管正在进行抗菌治疗,经食管超声心动图未显示任何减少的植被的大小。因此,患者接受了手术治疗。最初进行腹腔镜左肾上腺切除术。患者的血压随着肿瘤周围的充气和操作而升高,但在肾上腺肿瘤切除后立即下降。肾上腺切除术后,建立了体外循环。二尖瓣主动脉瓣小叶连同植被全部切除。随后,植入了一个机械主动脉瓣。手术后两天内,肌力药物完全停用。病理检查证实肾上腺偶发瘤为嗜铬细胞瘤。对于诊断为感染性心内膜炎的嗜铬细胞瘤患者,心脏手术前一期肾上腺切除术联合体外循环可能是一种有效的策略。此外,通过在心脏手术前尽可能多地控制患者的全身状况,它可以降低嗜铬细胞瘤并发症的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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