首页> 美国卫生研究院文献>Oxford Medical Case Reports >Spontaneous hepatic artery dissection—a rare presentation of fibromuscular dysplasia
【2h】

Spontaneous hepatic artery dissection—a rare presentation of fibromuscular dysplasia

机译:自发性肝动脉夹层—罕见的纤维肌增生异常表现

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Fibromuscular dysplasia (FMD) is a rare condition that causes structural compromise of the blood vessel presenting either as an incidental radiological finding, dissection or stenosis usually of the renal or craniocervical arteries. Seldom, patients present with spontaneous dissection in visceral arteries and there are few reports of hepatic involvement. This report outlines the case of a 43-year-old female who presented with severe right upper quadrant pain with a subsequent diagnosis of FMD manifesting as spontaneous hepatic artery dissection. The patient was treated with conservative antiplatelet therapy and regular radiographic follow-up, decided by the treating team as no clear guidelines exist for management of this particular presentation of FMD. Surgical management is not currently recommended to this patient due to the risk of further dissection, but may be considered if there is severe haemodynamic compromise or refractory pain.
机译:纤维肌发育不良(FMD)是一种罕见的疾病,会导致血管结构受损,表现为通常是肾或颅颈动脉的放射影像学发现,解剖或狭窄。很少有内脏动脉自发解剖的患者,很少有肝脏受累的报道。该报告概述了一名43岁女性的病例,该女性患有严重的右上腹疼痛,随后诊断为FMD,表现为自发性肝动脉夹层。由于治疗该FMD的具体方法尚无明确的指导方针,因此治疗团队决定对患者进行保守的抗血小板治疗和定期的影像学随访。由于存在进一步解剖的风险,目前不建议对该患者进行手术治疗,但是如果存在严重的血液动力学损害或难治性疼痛,可以考虑进行手术治疗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号