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冯·吉尔克病(I型糖原贮积病)与危及生命的腹主动脉瘤:一例极其罕见病症的病例报告

Von Gierke Disease (Glycogen Storage Disease Type I) and Life-Threatening Abdominal Aortic Aneurysm: A Case Report of an Extremely Rare Condition.

作者信息

Pitoulias Apostolos G, Bakr Nizar Abu, Kazemtash Majid, Dahi Firouza, Schütz Michael, Donas Konstantinos P

机构信息

Department of Vascular and Endovascular Surgery, Research Vascular Center, Asklepios Clinic Langen, Langen, Germany.

Department of Vascular Surgery, Bern University Hospital, Bern, Switzerland.

出版信息

Vasc Specialist Int. 2023 Jun 19;39:14. doi: 10.5758/vsi.230017.

Abstract

Von Gierke disease, also known as glycogen storage disease type I, co-existent with an abdominal aortic aneurysm (AAA), is an extremely rare combination of diseases that requires challenging therapeutic measures. We present, for the first time in literature, the case of a 62-year-old female with von Gierke disease who required open surgical repair of an AAA with challenging neck anatomy outside of instructions for use of endovascular repair. Even though the surgical risks for life-threatening complications, such as pancreatitis, metabolic acidosis, and kidney failure, were high, the 6-month postoperative course was uneventful. Despite the invasiveness of the treatment, surgery to treat the AAA was safe and effective. Further data is needed to draw robust conclusions about the treatment of choice for those patients with diseases in co-existence with AAAs.

摘要

冯·吉尔克病,也称为I型糖原贮积病,与腹主动脉瘤(AAA)并存,是一种极为罕见的疾病组合,需要采取具有挑战性的治疗措施。我们首次在文献中报道了一例62岁患有冯·吉尔克病的女性病例,该患者因颈部解剖结构复杂,不符合血管内修复的使用说明,而需要进行AAA开放手术修复。尽管发生胰腺炎、代谢性酸中毒和肾衰竭等危及生命并发症的手术风险很高,但术后6个月的病程平稳。尽管治疗具有侵入性,但治疗AAA的手术是安全有效的。需要更多数据才能就那些同时患有AAA疾病的患者的首选治疗方法得出有力结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc41/10277830/1283e514aa42/vsi-39-14-f1.jpg

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