Lee Jong Ha, Kim Eunkuk, Chon Suk
Department of Physical Medicine and Rehabilitation, Kyung Hee University School of Medicine, Seoul, Korea.
Department of Physical Education, Korea National Sport University, Seoul, Korea.
Ann Rehabil Med. 2015 Oct;39(5):826-32. doi: 10.5535/arm.2015.39.5.826. Epub 2015 Oct 26.
We describes a patient with hypokalemia-induced rhabdomyolysis due to primary aldosteronism (PA), who suffered from slowly progressive muscle weakness after laparoscopic adrenalectomy, and was later diagnosed with coexisting sporadic inclusion body myositis (sIBM). A 54-year-old Asian male presented with severe muscle weakness of both lower extremities. Laboratory findings showed profound hypokalemia, and extreme elevation of the serum creatine phosphokinase levels, suggestive of hypokalemia-induced rhabdomyolysis. Further evaluation strongly suggested PA by an aldosterone-producing adenoma, which was successfully removed surgically. However, muscle weakness slowly progressed one year after the operation and a muscle biopsy demonstrated findings consistent with sIBM. This case is the first report of hypokalemia-induced rhabdomyolysis by PA coexistent with sIBM, to the best of our knowledge.
我们描述了一名因原发性醛固酮增多症(PA)导致低钾血症性横纹肌溶解的患者,该患者在腹腔镜肾上腺切除术后出现缓慢进展的肌肉无力,后来被诊断为合并散发性包涵体肌炎(sIBM)。一名54岁的亚洲男性出现双下肢严重肌肉无力。实验室检查发现严重低钾血症,血清肌酸磷酸激酶水平极度升高,提示低钾血症性横纹肌溶解。进一步评估强烈提示为醛固酮瘤所致的PA,通过手术成功切除。然而,术后一年肌肉无力仍缓慢进展,肌肉活检显示的结果与sIBM一致。据我们所知,该病例是PA导致的低钾血症性横纹肌溶解与sIBM并存的首例报告。