一个强烈而偶然的呼吸困难病例。

R Hammer, M Sciaudone
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引用次数: 0

摘要

病例:一名48岁男性,无既往病史。来自初级保健诊所的高血压急症200/130。该患者报告间歇性无生产性咳嗽,持续时间约为一年,上个月用力和矫直时呼吸困难加重,伴有下肢肿胀。值得注意的是,他20年前从洪都拉斯移民过来。在急诊科使用Lasix后血压恢复正常。体格检查显示双侧肺底有罗音,颈静脉扩张,下肢点状水肿伴蛇形红斑和擦伤,心脏跳动。实验室显示外周嗜酸性粒细胞增多、血小板减少、肌酐升高、高胆红素血症、高血糖和轻度转氨炎。经胸超声心动图显示左心室扩张,整体运动不足,收缩功能严重下降,射血分数低于15%。患者尿尿,随后左、右心导管置入正常。胸部CT示右上肺叶一小结节。球虫病、克氏锥虫和结核分枝杆菌检测呈阴性;而抗酸杆菌培养出的是福氏分枝杆菌。粪类圆线虫抗体试验阳性,患者口服伊维菌素2剂,静脉注射头孢曲松1剂,出院。两个月后,他的嗜酸性粒细胞减少,但他仍然有咳嗽和体重减轻的症状,并开始口服环丙沙星和甲氧苄啶-磺胺甲唑治疗福氏分枝杆菌的门诊疗程。讨论:类圆线虫感染的患者可携带寄生虫数年而无明显症状。圆形线虫在南美洲各地流行,通过自身感染的生命周期在其宿主中持续存在,随着时间的推移,寄生虫负担增加,并可导致过度感染综合征,其中丝状幼虫穿透器官组织,最常见的是:心脏、中枢神经系统、肺和肝脏。我们怀疑慢性嗜酸性粒细胞增多和弥散性丝虫病是该患者非缺血性扩张型心肌病的病因。圆线虫病的标准治疗是伊维菌素,然而,在过度感染综合征的情况下,由于短暂菌血症的死亡率很高。因此,在开始使用抗寄生虫剂之前,应考虑使用革兰氏阴性棒覆盖的菌血症预防。
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A Strong and Fortuitous Case of Dyspnea.

Case: A 48 year-old man with no past medical history was sent to our emergency department (ED); from a primary care clinic for hypertensive urgency of 200/130. The man reported an intermittent non-productive cough of approximately one year's duration and worsening dyspnea on exertion and orthopnea over the last month with lower extremity swelling. Of note, he emigrated from Honduras twenty years ago. Blood pressure normalized with administration of Lasix in the ED. Physical exam revealed rales in lung bases bilaterally, jugular venous distension, lower extremity pitting edema with serpiginous patches of erythema and excoriation, and a cardiac gallop. Labs showed peripheral eosinophilia, thrombocytopenia, elevated creatinine, hyperbilirubinemia, hyperglycemia, and mild transaminitis. Transthoracic echocardiogram revealed a dilated left ventricle with global hypokinesis and severely depressed systolic function with an ejection fraction less than 15 percent . The patient was diuresed, and subsequent left and right heart catheterizations were normal. CT chest showed a small nodule in the right upper lobe. Tests for Coccidiosis, Trypanosoma cruzi, and Mycobacterium tuberculosis were negative; however the acid fast bacilli culture grew Mycobacterium fortuitum. A Strongyloides stercoralis antibody test was positive, and the patient was treated with two doses of oral ivermectin with one dose of intravenous ceftriaxone, and discharged. Two months later, his eosinophilia resolved, but he remained symptomatic with productive cough and weight loss, and was started on an outpatient course of oral ciprofloxacin and trimethoprim-sulfamethozole for M. fortuitum.

Disscusion: Strongyloides-infected patients may carry the parasite for years without prominent symptoms. Endemic throughout South America, Strongyloides persists in its hosts through a lifecycle of autoinfection, which, over time, increases parasite burden and can lead to a hyperinfection syndrome whereby filiariform larvae penetrate organ tissue, most commonly: heart, central nervous system, lungs and liver. We suspect chronic eosinophilia and disseminated filiaria to be the etiology of the non-ischemic dilated cardiomyopathy in this patient. Standard treatment of strongyloidiasis is ivermectin, however, mortality owing to transient bacteremia in the setting of hyperinfection syndrome is high. Therefore, bacteremia prophylaxis with gram negative rod coverage should be considered before antiparasitic agent initiation.

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Where are we going? Refractory anemia. Urinary diversion. Schneiderian papilloma. Recurrent respiratory papillomatosis.
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