Suppr超能文献

二尖瓣置换术治疗持续性原发性抗磷脂综合征和复发性卒中患者的增大性 Libman-Sacks 心内膜炎:病例报告。

Mitral Valve Replacement for Enlarged Libman-Sacks Endocarditis in a Patient with Persistent Primary Antiphospholipid Syndrome and Recurrent Stroke: A Case Report.

机构信息

Department of Neurology, Nara Medical University, Kashihara, Nara, Japan.

Department of Thoracic and Cardiovascular Surgery, Nara Medical University, Kashihara, Nara, Japan.

出版信息

Am J Case Rep. 2023 Feb 6;24:e938930. doi: 10.12659/AJCR.938930.

Abstract

BACKGROUND Anticardiolipin antibodies in patients with Libman-Sacks endocarditis (LS) are indicative of comorbid antiphospholipid syndrome (APS) and can result in cerebral infarctions. We describe a case of LS and primary APS with recurrent cerebral infarctions despite anticoagulation treatment. The patient underwent surgery for enlarged LS vegetation with high titers of antiphospholipid antibodies. CASE REPORT A 41-year-old Japanese man was admitted to hospital for small cerebral infarction recurrence in a left parietal lesion. At age 35, the patient had suffered multiple cerebral infarctions. He was found to have high serum titers of all 3 antiphospholipid antibodies. Transesophageal echocardiography (TEE) findings were normal. Differential diagnosis ruled out other autoimmune diseases and a clinical diagnosis of primary APS was made. Warfarin anticoagulation was started. When cerebral infarction recurred 6 years after the first episode, serum titers of antiphospholipid antibodies remained high, and TEE showed a 7×8 mm area of mitral vegetation. A TEE results from his first admission revealed a 5×6 mm area of mitral vegetation, which was believed to be related to the current vegetation. As anticoagulation produced no improvement, the mitral valve was replaced with a mechanical valve. Examination of the excised vegetation found it to be consistent with LS. The patient made good progress within 3 years after surgery. CONCLUSIONS LS size can increase despite anticoagulation in cases with high titers of all 3 antiphospholipid antibodies and cerebral infarction. Such patients require ongoing TEE follow-up and surgical treatment should be considered.

摘要

背景

伴有脑梗死的 Libman-Sacks 心内膜炎(LS)患者的抗心磷脂抗体提示合并存在抗磷脂综合征(APS),并可能导致脑梗死。我们描述了一例 LS 和原发性 APS 患者,尽管接受抗凝治疗,但仍反复发生脑梗死。该患者因伴有高滴度抗磷脂抗体的 LS 赘生物而接受手术治疗。

病例报告

一名 41 岁的日本男性因左顶叶小面积脑梗死复发而入院。35 岁时,患者曾多次发生脑梗死。他的血清中所有 3 种抗磷脂抗体的滴度均较高。经食管超声心动图(TEE)检查未见异常。鉴别诊断排除了其他自身免疫性疾病,并作出原发性 APS 的临床诊断。开始给予华法林抗凝治疗。首次发病 6 年后再次发生脑梗死时,抗磷脂抗体滴度仍较高,TEE 显示二尖瓣赘生物 7×8mm。首次入院的 TEE 结果显示二尖瓣赘生物 5×6mm,推测与目前的赘生物有关。由于抗凝治疗无改善,故用机械瓣替换二尖瓣。切除的赘生物检查结果与 LS 一致。术后 3 年内,患者病情恢复良好。

结论

在伴有高滴度 3 种抗磷脂抗体和脑梗死的情况下,尽管进行抗凝治疗,LS 大小仍可能增大。此类患者需要持续进行 TEE 随访,且应考虑手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4557/9909611/22b98ef30c26/amjcaserep-24-e938930-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验