Baek Joo Eun, Park Dong Jun, Kim Hyun-Jin, Lee Jong Denog, Chang Se-Ho
Department of Internal Medicine, College of Medicine, Gyeongsang National University, Jinju, South Korea.
J Clin Gastroenterol. 2007 Mar;41(3):317-21. doi: 10.1097/01.mcg.0000225615.71599.74.
We have frequently seen idiopathic rhabdomyolysis developed after liver cirrhosis (LC) in our hospital. This has rarely been reported, and no studies have compared it with other cases of rhabdomyolysis.
We attempted to examine the pathologic characteristics of rhabdomyolysis development and to assess the prognosis in patients with LC.
We retrospectively reviewed the medical records of 243 patients (261 cases) with rhabdomyolysis and selected 74 patients (91 cases) for the study group, who concurrently had LC. Seventy-five patients (76 cases) with no evidence of LC were served as controls.
In 59.3% of the LC-group patients, the causes of rhabdomyolysis were not identified. In 10.5% of the control-group patients, the causes of rhabdomyolysis proved to be unknown (P=0.000). In 17.6% of the LC-group patients, 30 cases (33.0%) of the recurrent rhabdomyolysis were identified. In the control group, only one case of the recurrent rhabdomyolysis was noted (P=0.001). The mortality was significantly higher in the LC group than the control group (27.5% vs. 14.5%) (P=0.042). Of 25 LC-group patients who died, 96.0% had Child-Pugh classification C. In addition, 84.0% developed acute renal failure during the course. Coexistent infection, hepatic encephalopathy, and the elevated levels of serum lactate dehydrogenase and C-reactive protein were also important prognostic factors.
In conclusion, rhabdomyolysis is developed without specific causes in patients with LC, and it is serious and often fatal particularly in cases in which acute renal failure and severe hepatic dysfunction exist. Our results indicate that LC is the underlying disease for the development of rhabdomyolysis.
在我院,我们经常见到肝硬化(LC)后发生特发性横纹肌溶解症。这种情况鲜有报道,且尚无研究将其与其他横纹肌溶解症病例进行比较。
我们试图研究横纹肌溶解症发生的病理特征,并评估LC患者的预后。
我们回顾性分析了243例(261例次)横纹肌溶解症患者的病历,选取了74例(91例次)同时患有LC的患者作为研究组。75例(76例次)无LC证据的患者作为对照组。
在LC组患者中,59.3%的横纹肌溶解症病因不明。在对照组患者中,10.5%的横纹肌溶解症病因不明(P = 0.000)。在LC组患者中,17.6%(30例,占33.0%)出现复发性横纹肌溶解症。在对照组中,仅发现1例复发性横纹肌溶解症(P = 0.001)。LC组的死亡率显著高于对照组(27.5%对14.5%)(P = 0.042)。在25例死亡的LC组患者中,96.0%的患者Child-Pugh分级为C级。此外,84.0%的患者在病程中发生了急性肾衰竭。合并感染、肝性脑病以及血清乳酸脱氢酶和C反应蛋白水平升高也是重要的预后因素。
总之,LC患者发生横纹肌溶解症无特定病因,且病情严重,常为致命性,尤其是在存在急性肾衰竭和严重肝功能障碍的情况下。我们的结果表明,LC是横纹肌溶解症发生的基础疾病。