López Herrero R, Rodríguez Jiménez R P, Sánchez Quirós B
Servicio de Anestesiología y Reanimación. Hospital Clínico Universitario de Valladolid, Valladolid, España.
Servicio de Anestesiología y Reanimación. Hospital Clínico Universitario de Valladolid, Valladolid, España.
Rev Esp Anestesiol Reanim (Engl Ed). 2021 Mar 11. doi: 10.1016/j.redar.2020.12.013.
Pheochromocytomas are rare neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla. Most adrenal pheochromocytomas secrete norepinephrine and epinephrine. Dopamine secreting pheochromocytomas are extremely rare and differs from classic pheochromocytomas in clinical features, posing a significant diagnostic challenge. A 41-year-old women presented to our emergency department because of acute flank colic pain and normotension. The screening abdominal computed tomography scan revealed a left adrenal mass. The laboratory test showed significantly increase in plasma dopamine and 24-hour urine dopamine. During surgical removal the patient remained hypotensive requiring doses of norepinephrine. The patient presented significant hypertensive responde during direct laryngoscopy and intubation.
嗜铬细胞瘤是起源于肾上腺髓质嗜铬细胞的罕见神经内分泌肿瘤。大多数肾上腺嗜铬细胞瘤分泌去甲肾上腺素和肾上腺素。分泌多巴胺的嗜铬细胞瘤极为罕见,在临床特征上与经典嗜铬细胞瘤不同,构成了重大的诊断挑战。一名41岁女性因急性胁腹绞痛和血压正常就诊于我们的急诊科。腹部计算机断层扫描筛查显示左肾上腺有肿块。实验室检查显示血浆多巴胺和24小时尿多巴胺显著升高。手术切除过程中患者持续低血压,需要使用去甲肾上腺素。患者在直接喉镜检查和插管期间出现明显的高血压反应。