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肝动脉栓塞术治疗遗传性出血性毛细血管扩张症合并有症状的肝血管畸形患者。

Hepatic artery embolization for treatment of patients with hereditary hemorrhagic telangiectasia and symptomatic hepatic vascular malformations.

作者信息

Chavan Ajay, Caselitz Martin, Gratz Karl-Friedrich, Lotz Joachim, Kirchhoff Timm, Piso Plinio, Wagner Siegfried, Manns Michael, Galanski Michael

机构信息

Department of Diagnostic Radiology, Hannover Medical School, Hannover, Germany.

出版信息

Eur Radiol. 2004 Nov;14(11):2079-85. doi: 10.1007/s00330-004-2455-5. Epub 2004 Aug 17.

Abstract

At present there is no established therapy for treating patients with hereditary hemorrhagic telangiectasia (HHT) and symptomatic hepatic involvement. We present the results of a prospective study with 15 consecutive patients who were treated with staged hepatic artery embolization (HAE). Branches of the hepatic artery were selectively catheterized and embolized in stages using polyvinyl alcohol particles (PVA) and platinum microcoils or steel macrocoils. Prophylactic antibiotics, analgesics and anti-emetics were administered after every embolization. Clinical symptomatology and cardiac output were assessed before and after therapy as well as at the end of follow-up (median 28 months; range 10-136 months). Five patients had abdominal pain and four patients had symptoms of portal hypertension. The cardiac output was raised in all patients, with cardiac failure being present in 11 patients. After treatment, pain resolved in all five patients, and portal hypertension improved in two of the four patients. The mean cardiac output decreased significantly ( P<0.001) from 12.57+/-3.27 l/min pre-treatment to 8.36+/-2.60 l/min at the end of follow-up. Symptoms arising from cardiac failure resolved or improved markedly in all but one patient. Cholangitis and/or cholecystitis occurred in three patients of whom two required a cholecystectomy. One patient with pre-existent hepatic cirrhosis died as a complication of the procedure. Staged HAE yields long-term relief of clinical symptoms in patients with HHT and hepatic involvement. Patients with pre-existing hepatic cirrhosis may be poor candidates for HAE.

摘要

目前,对于遗传性出血性毛细血管扩张症(HHT)合并有症状性肝脏受累的患者,尚无既定的治疗方法。我们报告了一项对15例连续患者进行分期肝动脉栓塞术(HAE)治疗的前瞻性研究结果。肝动脉分支被选择性插管,并使用聚乙烯醇颗粒(PVA)和铂微线圈或钢大线圈进行分期栓塞。每次栓塞后给予预防性抗生素、镇痛药和止吐药。在治疗前、治疗后以及随访结束时(中位时间28个月;范围10 - 136个月)评估临床症状和心输出量。5例患者有腹痛,4例患者有门静脉高压症状。所有患者的心输出量均升高,11例患者存在心力衰竭。治疗后,5例患者的疼痛均缓解,4例患者中有2例门静脉高压得到改善。平均心输出量从治疗前的12.57±3.27升/分钟显著下降(P<0.001)至随访结束时的8.36±2.60升/分钟。除1例患者外,所有心力衰竭引起的症状均明显缓解或改善。3例患者发生胆管炎和/或胆囊炎,其中2例需要行胆囊切除术。1例既往有肝硬化的患者死于该手术并发症。分期HAE可使HHT合并肝脏受累的患者临床症状得到长期缓解。既往有肝硬化的患者可能不是HAE的理想候选者。

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