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棘球蚴病的罕见表现:关于动脉型包虫囊肿的系统评价

Rare Presentation of Echinococcal Disease: A Systematic Review on Arterial Hydatid Cyst.

作者信息

Rascio Laura, Donati Tommaso, Pascucci Domenico, Sposato Francesco, Minucci Marta, Borghese Ottavia, Tshomba Yamume

机构信息

Unit of Vascular Surgery, Department of Cardiovascular and Pulmonary Sciences - Università Cattolica del Sacro Cuore, Rome, Italy.

Unit of Vascular Surgery, Department of Cardiovascular Sciences - Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

出版信息

Ann Vasc Surg. 2025 Mar;112:22-31. doi: 10.1016/j.avsg.2024.11.095. Epub 2024 Dec 13.

Abstract

BACKGROUND

Echinococcosis is a parasitic disease caused by Echinococcus granulosus that most commonly affects the liver (70%) and lungs (20%). Despite rarely reported, arterial echinococcosis represents a severe and potentially life-threatening condition but management strategies and related outcomes have not been fully investigated.

METHODS

A comprehensive review of the international English literature was performed on PubMed, Scopus, and Web of Science from inception to May 30, 2024 to identify relevant articles about arterial echinococcosis. Data regarding epidemiology, pathogenesis, clinical presentation, diagnostic methods, and treatment were investigated.

RESULTS

A total of 143 articles were screened and 30 articles were included. Overall 32 cases were identified. About half of the patients were female (18, 56.2%) and the mean age was 40.6 years (range 12-60 years). Echinococcus cyst was more commonly detected on the aorta (27, 84.3%) in association or not with other cysts on the iliofemoral axis. Five cases (15.2%) affected only peripheral arteries. Most patients presented with chronic pain due to vascular obstruction or thromboembolism, while one patient was asymptomatic. In most cases (31, 96.8%) a total surgical excision was done in association with antiparasitic treatment using albendazole (17, 53.1%) or mebendazole (4, 12.5%). Arterial reconstruction was required in 19 cases (59.4%) and done with prosthetic substitutes or bovine pericardium. Only one case (3%) was treated with an endovascular approach. Four patients (12.5%) died in-hospital from hemorrhagic shock (3) or respiratory failure (1). During the follow-up period (mean 14 months, range 2-72 months) only one recurrence was reported.

CONCLUSIONS

Arterial echinococcosis is an extremely rare condition that may potentially be lethal. The current review showed favorable outcomes following complete surgical excision and antiparasitic drug that currently remain the only definitive treatment.

摘要

背景

包虫病是由细粒棘球绦虫引起的一种寄生虫病,最常累及肝脏(70%)和肺(20%)。尽管动脉型包虫病报道较少,但它是一种严重且可能危及生命的疾病,其治疗策略和相关预后尚未得到充分研究。

方法

对PubMed、Scopus和Web of Science上从创刊至2024年5月30日的国际英文文献进行全面检索,以确定有关动脉型包虫病的相关文章。调查了有关流行病学、发病机制、临床表现、诊断方法和治疗的数据。

结果

共筛选出143篇文章,纳入30篇。共确定32例病例。约一半患者为女性(18例,56.2%),平均年龄为40.6岁(范围12 - 60岁)。棘球蚴囊肿更常见于主动脉(27例,84.3%),可伴有或不伴有髂股轴上的其他囊肿。5例(15.2%)仅累及外周动脉。大多数患者因血管阻塞或血栓栓塞出现慢性疼痛,1例患者无症状。在大多数病例(31例,96.8%)中,进行了完整手术切除,并联合使用阿苯达唑(17例,53.1%)或甲苯达唑(4例,12.5%)进行抗寄生虫治疗。19例(59.4%)需要进行动脉重建,采用人工替代物或牛心包进行。仅1例(3%)采用血管内介入治疗。4例患者(12.5%)因失血性休克(3例)或呼吸衰竭(1例)在医院死亡。在随访期间(平均14个月,范围2 - 72个月),仅报告1例复发。

结论

动脉型包虫病是一种极其罕见的疾病,可能具有致命性。目前的综述显示,完整手术切除和抗寄生虫药物治疗后预后良好,目前这仍然是唯一的确定性治疗方法。

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