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Wilson病脾功能亢进的成功脾切除术:来自中国的单中心经验

Successful Splenectomy for Hypersplenism in Wilson's Disease: A Single Center Experience from China.

作者信息

Li Liang-Yong, Yang Wen-Ming, Chen Huai-Zhen, Wu Yun-Hu, Fang Xiang, Zhang Jing, Wang Zhen, Han Yong-Sheng, Wang Yu

机构信息

Department of Neurology, the First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei 230031, China.

Department of General Surgery, the First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hefei 230031, China.

出版信息

PLoS One. 2015 Apr 24;10(4):e0124569. doi: 10.1371/journal.pone.0124569. eCollection 2015.

Abstract

Splenomegaly and pancytopenia are common in Wilson's disease (WD) and splenectomy is one of the conventional treatments for splenomegaly and the associated pancytopenia. However, splenectomy remained controversial for hypersplenism in WD as it was reported that splenectomy leaded to serious emotional and neurological deterioration in WD patients with hypersplenism. In the current study, we present our experiences in 70 WD patients with hypersplenism who had undergone splenectomy, outlining the safety and efficacy of splenectomy in WD. The clinical database of 70 WD patients with hypersplenism who had undergone splenectomy in our hospital between 2009 and 2013 were reviewed and followed-up regularly. Before splenectomy, all the patients accepted a short period of anti-copper treatment with intravenous sodium 2, 3-dimercapto-1-propane sulfonate (DMPS). All the patients demonstrated a marked improvement in platelet and leucocyte counts after splenectomy. No severe postoperative complication was observed. In particular, none of the 37 patients with mixed neurologic and hepatic presentations experienced neurological deterioration after splenectomy, and none of the patients with only hepatic presentations newly developed neurological symptoms. During the one year follow-up period, no patient presented hepatic failure or hepatic encephalopathy, no hepatic patient newly developed neurological presentations, and only 3 patients with mixed neurologic and hepatic presentations suffered neurological deterioration and these 3 patients had poor compliance of anti-copper treatment. Quantative analysis of the neurological symptoms in the 37 patients using the Unified Wilson's Disease Rating Scale (UWDRS) showed that the neurological symptoms were not changed in a short-term of one week after splenectomy but significantly improved in a long-term of one year after splenectomy. Additionally, compared to that before splenectomy, the esophageal gastric varices in most patients significantly improved one year after splenectomy. Thus, we may conclude that splenectomy is a safe and effective therapeutic measure for hypersplenism in WD patients who had been preoperatively treated with DMPS for powerful anti-copper therapy.

摘要

脾肿大和全血细胞减少在肝豆状核变性(WD)中很常见,脾切除术是治疗脾肿大及相关全血细胞减少的传统方法之一。然而,脾切除术治疗WD脾功能亢进仍存在争议,因为有报道称,脾切除术会导致WD脾功能亢进患者出现严重的情绪和神经功能恶化。在本研究中,我们介绍了70例接受脾切除术的WD脾功能亢进患者的经验,概述了脾切除术治疗WD的安全性和有效性。回顾并定期随访了2009年至2013年期间在我院接受脾切除术的70例WD脾功能亢进患者的临床数据库。脾切除术前,所有患者均接受了短期静脉注射二巯丙磺钠(DMPS)的驱铜治疗。所有患者脾切除术后血小板和白细胞计数均有显著改善。未观察到严重的术后并发症。特别是,37例有神经和肝脏混合表现的患者在脾切除术后均未出现神经功能恶化,仅肝脏表现的患者也均未新出现神经症状。在一年的随访期内,无患者出现肝衰竭或肝性脑病,肝脏表现的患者均未新出现神经表现,仅3例有神经和肝脏混合表现的患者出现神经功能恶化,且这3例患者驱铜治疗依从性差。使用统一的肝豆状核变性评定量表(UWDRS)对37例患者的神经症状进行定量分析显示,脾切除术后一周内神经症状无短期变化,但术后一年长期显著改善。此外,与脾切除术前相比,大多数患者脾切除术后一年食管胃静脉曲张明显改善。因此,我们可以得出结论,对于术前接受DMPS强力驱铜治疗的WD患者,脾切除术是治疗脾功能亢进的一种安全有效的治疗措施。

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