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内脏皮肤利什曼病合并心肌炎:病例报告。

Viscerocutaneous Loxoscelism Manifesting with Myocarditis: A Case Report.

机构信息

University of Kansas School of Medicine, Kansas City, KS, USA.

Department of Pediatrics, Division of Pediatric Critical Care, University of Kansas Medical Center, Kansas City, KS, USA.

出版信息

Am J Case Rep. 2021 Aug 28;22:e932378. doi: 10.12659/AJCR.932378.

Abstract

BACKGROUND Envenomation from the brown recluse spider (Loxosceles reclusa) is described to cause both local and systemic symptoms. We report a case of an adolescent boy who developed severe systemic loxoscelism, and his clinical course was complicated by myocarditis, which has not been previously reported in association with loxoscelism. CASE REPORT A 16-year-old boy presented with non-specific symptoms and forearm pain following a suspected spider bite, which subsequently evolved into a necrotic skin lesion. During his clinical course, he developed a characteristic syndrome of systemic loxoscelism with hemolysis, disseminated intravascular coagulopathy, and severe systemic inflammatory response syndrome, necessitating transfer to the Intensive Care Unit. The diagnosis was confirmed with an enzyme-linked immunosorbent assay that detected Loxosceles venom in the wound. Additionally, he developed pulmonary edema and cardiogenic shock secondary to myocarditis, which was confirmed with cardiac magnetic resonance imaging. Steroids and plasmapheresis were initiated to manage the severe inflammatory syndrome, and the myocarditis was treated with intravenous immunoglobulins, resulting in resolution of symptoms and improvement of cardiac function. CONCLUSIONS This is the first reported case of myocarditis associated with loxoscelism, providing evidence for Loxosceles toxin-associated cardiac injury, which has been previously described in animal models only. Furthermore, this case provides further support for the use of confirmatory testing in the clinical diagnosis of loxoscelism.

摘要

背景

褐隐士蜘蛛(Loxosceles reclusa)引起的咬伤会导致局部和全身症状。我们报告了一例青少年男性发生严重全身利什曼病的病例,他的临床病程还并发了心肌炎,这在与利什曼病相关的病例中尚未有报道。

病例报告

一名 16 岁男孩在疑似被蜘蛛咬伤后出现非特异性症状和前臂疼痛,随后发展为坏死性皮肤病变。在他的临床病程中,他出现了全身利什曼病的特征性综合征,伴有溶血、弥散性血管内凝血和严重的全身炎症反应综合征,需要转入重症监护病房。通过酶联免疫吸附试验检测到伤口中的利什曼蛇毒,确诊了该疾病。此外,他还因心肌炎继发肺水肿和心源性休克,心脏磁共振成像证实了这一诊断。他接受了类固醇和血浆置换治疗以控制严重的炎症综合征,心肌炎则使用静脉注射免疫球蛋白治疗,症状和心功能均得到了改善。

结论

这是首例与利什曼病相关的心肌炎病例,为利什曼蛇毒相关的心脏损伤提供了证据,此前仅在动物模型中有所描述。此外,该病例进一步支持了在利什曼病的临床诊断中使用确认性检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcde/8409453/d256ebc944bb/amjcaserep-22-e932378-g001.jpg

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