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一种罕见疾病的不寻常表现:急性上肢缺血作为 Whipple 心内膜炎的首发症状,一例报告。

An unusual presentation of a rare disease: acute upper limb ischemia as the presenting symptom of Whipple's Endocarditis, a case report.

机构信息

Department of Medicine, Dartmouth-Hitchcock Medical Center, 1 Medical Center Dr, Lebanon, NH, 03766, USA.

出版信息

BMC Infect Dis. 2023 Mar 27;23(1):180. doi: 10.1186/s12879-023-08148-5.

Abstract

BACKGROUND

Whipple's disease is known to cause multiple varied systemic symptoms, and is a well-documented cause of culture-negative endocarditis. Endocarditis secondary to Whipple disease, however, has rarely been known to present primarily as a cause of acute limb ischemia. We describe such a case here.

CASE PRESENTATION

A previously healthy 40 year old man presented to the emergency department with acute-onset right arm paresthesias. On exam, he was found to be tachycardic with a VI/VI systolic ejection murmur. He was diagnosed with critical limb ischemia and severe aortic regurgitation, and echocardiography showed a large mass on his bicuspid aortic valve. Thrombectomy was performed urgently, with aortic valve repair the following day. As blood cultures and valvular tissue culture remained unrevealing, the patient remained on empiric vancomycin and ceftriaxone for culture-negative endocarditis. 16 s rRNA nucleic acid amplification testing (NAAT) of his formalin-fixed, paraffin-embedded valvular tissue detected T. whipplei, after which the patient was transitioned to ceftriaxone and trimethoprim-sulfamethoxazole for a year of therapy. He continues to do clinically well.

CONCLUSIONS

We report an unusual presentation of Whipple endocarditis as an acute upper limb ischemia, absent other classic symptoms of Whipple's disease, and with diagnosis made by 16 s rRNA NAAT of valvular tissue in the setting of culture-negative endocarditis.

摘要

背景

已知 Whipple 病可引起多种不同的全身症状,是无菌性心内膜炎的明确病因。然而,Whipple 病继发的心内膜炎很少作为急性肢体缺血的主要原因。我们在此介绍这样一个病例。

病例介绍

一名既往健康的 40 岁男性因急性右上肢感觉异常就诊于急诊科。体格检查发现患者心动过速,伴有 VI/VI 级收缩期喷射样杂音。诊断为严重肢体缺血和重度主动脉瓣反流,超声心动图显示患者的二叶式主动脉瓣上有一个大肿块。紧急进行了血栓切除术,次日进行了主动脉瓣修复术。由于血培养和瓣膜组织培养均无结果,患者仍接受经验性万古霉素和头孢曲松治疗无菌性心内膜炎。对患者经福尔马林固定、石蜡包埋的瓣膜组织进行 16s rRNA 核酸扩增检测(NAAT),检测到 T. whipplei,此后患者转为头孢曲松和甲氧苄啶-磺胺甲噁唑治疗 1 年。他的临床状况持续改善。

结论

我们报告了 Whipple 心内膜炎的一种不常见表现,即急性上肢缺血,缺乏 Whipple 病的其他典型症状,并且在无菌性心内膜炎背景下,通过瓣膜组织的 16s rRNA NAAT 诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5387/10041733/bf79b62f8a3c/12879_2023_8148_Fig1_HTML.jpg

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