Wen Zhang, Chuanwei Li, Chunyu Zeng, Hui Huang, Weimin Li
Department of Respiratory, West China Hospital, Sichuan University, Chengdu, PR China.
BMC Res Notes. 2013 Apr 17;6:155. doi: 10.1186/1756-0500-6-155.
Rhabdomyolysis presenting with severe hypokalemia as the first manifestation of primary hyperaldosteronism is extremely rare.
Two middle-aged Chinese females were admitted to our emergency department for muscular weakness and limb pain, and both have the history of early onset hypertension. Laboratory test showed elevated creatinine phosphokinase (4, 907 and 8, 531 IU/L) and extremely low serum potassium (1.38 mmol/L and 1.98 mmol/L). Rhabdomyolysis and severe hypokalemia were established as first diagnosis. Hypokalemic rhabdomyolysis was confirmed after nervous system disorders, autoimmune diseases and trauma were excluded. Adrenal computerized tomography scan and postural stimulation test revealed aldosterone-producing adenomas. They both received laparoscopic adrenalectomy and were stable at the 2-year follow-up visit.
The two cases remind physicians to bear in mind the risk of hypokalemia-induced rhabdomyolysis among patients with primary hyperaldosteronism.
以严重低钾血症为原发性醛固酮增多症首发表现的横纹肌溶解症极为罕见。
两名中国中年女性因肌无力和肢体疼痛入住我院急诊科,两人均有早发性高血压病史。实验室检查显示肌酸磷酸激酶升高(4907和8531 IU/L),血清钾极低(1.38 mmol/L和1.98 mmol/L)。横纹肌溶解症和严重低钾血症被确立为初步诊断。在排除神经系统疾病、自身免疫性疾病和创伤后,低钾性横纹肌溶解症得到确诊。肾上腺计算机断层扫描和体位刺激试验显示醛固酮瘤。她们均接受了腹腔镜肾上腺切除术,在2年随访时情况稳定。
这两例病例提醒医生应牢记原发性醛固酮增多症患者发生低钾血症诱发横纹肌溶解症的风险。