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自发性孤立性腹腔干和脾动脉夹层伴脾梗死

Spontaneous isolated celiac and splenic artery dissection with splenic infarction.

作者信息

Pateman Aciu Shaun, Petrochko Jameson, Bassik Noy, Fisher Jay

机构信息

Temple/St. Luke's School of Medicine, 800 Ostrum St., Bethlehem, PA 18015, USA.

Department of Surgery, St. Luke's University Health Network, Bethlehem, PA, USA.

出版信息

Radiol Case Rep. 2022 Apr 12;17(6):2085-2091. doi: 10.1016/j.radcr.2022.03.060. eCollection 2022 Jun.

Abstract

Spontaneous isolated celiac artery dissection is considered an uncommon clinical condition. Rarer still is spontaneous isolated celiac and splenic artery dissection, with a total of 42 reported cases. There is no known definitive cause of visceral artery dissections, but risk factors include male sex, age in 5th or 6th decade, hypertension, and connective tissue disorders. The presentation varies, diagnosis is principally radiographic, and the mainstay of treatment is anticoagulation or antiplatelet therapy. Splenic infarction is a common finding with splenic artery dissection, although the strength of this association has not previously been reported. Herein we present a case of spontaneous isolated celiac and splenic artery dissection with splenic infarction that was successfully managed with blood pressure control and antiplatelet therapy. We review previous literature, principles of diagnosis and management, and incidence and outcomes of splenic infarction as it related to splenic artery dissection.

摘要

自发性孤立性腹腔干动脉夹层被认为是一种不常见的临床病症。更为罕见的是自发性孤立性腹腔干和脾动脉夹层,总共仅有42例报道。目前尚不清楚内脏动脉夹层的确切病因,但危险因素包括男性、50或60岁、高血压以及结缔组织疾病。临床表现各异,诊断主要依靠影像学检查,治疗的主要方法是抗凝或抗血小板治疗。脾梗死是脾动脉夹层常见的表现,尽管此前尚未报道过这种关联的强度。在此,我们报告一例自发性孤立性腹腔干和脾动脉夹层伴脾梗死的病例,该病例通过血压控制和抗血小板治疗成功治愈。我们回顾了既往文献、诊断和治疗原则以及与脾动脉夹层相关的脾梗死的发生率和转归。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acd/9018800/349290901d1b/gr1a.jpg

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