Tarant Nicki S, Dacanay Rhodel G, Mecklenburg Brian W, Birmingham Sean D, Lujan Eugenio, Green Richard
Department of Anesthesiology, Naval Medical Center San Diego, San Diego, California 92134-1005, USA.
Anesth Analg. 2006 Feb;102(2):642-3. doi: 10.1213/01.ane.0000184827.79120.43.
Pheochromocytoma is a rare catecholamine-producing tumor that can cause severe hypertension and other systemic disturbances. A clinical challenge arises when a patient with a previously undiagnosed and untreated pheochromocytoma presents with a surgical emergency. We describe a patient presenting with acute appendicitis in whom surgery was cancelled because of suspected pheochromocytoma. The possibility of mortality associated with surgery in a patient with an undiagnosed pheochromocytoma outweighed the risk of nonoperative management for appendicitis. This case resulted in a nonoperative resolution of appendicitis and an unremarkable recovery once appropriate hypertension treatment was administered.
嗜铬细胞瘤是一种罕见的分泌儿茶酚胺的肿瘤,可导致严重高血压和其他全身紊乱。当一名先前未诊断和未治疗的嗜铬细胞瘤患者出现外科急症时,就会出现临床挑战。我们描述了一名表现为急性阑尾炎的患者,其手术因疑似嗜铬细胞瘤而取消。未诊断出嗜铬细胞瘤的患者手术相关的死亡可能性超过了阑尾炎非手术治疗的风险。该病例导致阑尾炎非手术治愈,在给予适当的高血压治疗后恢复良好。