Zern Nicole K, Eaton Keith D, Roth Mara Y
Division of General Surgery, Department of Surgery, University of Washington, Seattle, Washington.
Division of Medical Oncology, Department of Medicine, University of Washington, Seattle, Washington.
J Endocr Soc. 2019 Jun 12;3(9):1678-1681. doi: 10.1210/js.2019-00092. eCollection 2019 Sep 1.
Adrenocortical carcinoma (ACC) is a rare malignancy that usually is detected as a result of symptoms of hormone excess or mass effect. We describe a rare presentation of ACC with primary aldosterone production leading to profound hypokalemia and cardiac arrest. The patient was previously asymptomatic with low-grade, untreated hypertension and no documented electrolyte abnormalities. She had sudden cardiac arrest, and potassium levels were undetectable. After successful resuscitation, imaging showed a 6-cm left adrenal mass highly suspicious for malignancy. Biochemical workup revealed aldosterone excess as well as cortisol excess, despite the absence of Cushingoid symptoms. Histopathological examination after surgical resection demonstrated high-grade ACC. This case illustrates that the workup of cardiac arrest as a result of electrolyte abnormalities should include evaluation for adrenal pathology.
肾上腺皮质癌(ACC)是一种罕见的恶性肿瘤,通常因激素过多症状或占位效应而被发现。我们描述了一例罕见的ACC病例,其主要分泌醛固酮,导致严重低钾血症和心脏骤停。该患者之前无症状,患有轻度、未经治疗的高血压,且无电解质异常记录。她突然发生心脏骤停,血钾水平无法检测到。成功复苏后,影像学检查显示左侧肾上腺有一个6厘米的肿块,高度怀疑为恶性肿瘤。生化检查显示醛固酮和皮质醇均过量,尽管没有库欣综合征症状。手术切除后的组织病理学检查显示为高级别ACC。该病例表明,对因电解质异常导致的心脏骤停进行检查时,应包括对肾上腺病变的评估。