Moffatt Cameron R M, Moloi Soniah B, Kennedy Karina J
National Centre for Epidemiology and Population Health, Research School of Population Health, Australian National University, Canberra, 2602, ACT, Australia.
Department of Cardiology, Canberra Hospital and Health Services, Canberra, 2605, ACT, Australia.
BMC Infect Dis. 2017 Jan 5;17(1):8. doi: 10.1186/s12879-016-2115-9.
Campylobacter spp. are a common cause of mostly self-limiting enterocolitis. Although rare, pericarditis and myopericarditis have been increasingly documented as complications following campylobacteriosis. Such cases have occurred predominantly in younger males, and involved a single causative species, namely Campylobacter jejuni. We report the first case of myopericarditis following Campylobacter coli enterocolitis, with illness occurring in an immunocompetent middle-aged female.
A 51-yo female was admitted to a cardiology unit with a 3-days history of chest pain. The woman had no significant medical history or risk factors for cardiac disease, nor did she report any recent overseas travel. Four days prior to the commencement of chest pain the woman had reported onset of an acute gastrointestinal illness, passing 3-4 loose stools daily, a situation that persisted at the time of presentation. Physical examination showed the woman's vital signs to be essentially stable, although she was noted to be mildly tachycardic. Laboratory testing showed mildly elevated C-reactive protein and a raised troponin I in the absence of elevation of the serum creatinine kinase. Electrocardiography (ECG) demonstrated concave ST segment elevations, and PR elevation in aVR and depression in lead II. Transthoracic echocardiogram (TTE) revealed normal biventricular size and function with no significant valvular abnormalities. There were no left ventricular regional wall motion abnormalities. No pericardial effusion was present but the pericardium appeared echodense. A diagnosis of myopericarditis was made on the basis of chest pain, typical ECG changes and troponin rise. The chest pain resolved and she was discharged from hospital after 2-days of observation, but with ongoing diarrhoea. Following discharge, a faecal sample taken during the admission, cultured Campylobacter spp. Matrix assisted laser desorption ionization time-of-flight (Bruker) confirmed the cultured isolate as C. coli.
We report the first case of myopericarditis with a suggested link to an antecedent Campylobacter coli enterocolitis. Although rare, myopericarditis is becoming increasingly regarded as a complication following campylobacteriosis. Our report highlights potential for pericardial disease beyond that attributed to Campylobacter jejuni. However uncertainty regarding pathogenesis, coupled with a paucity of population level data continues to restrict conclusions regarding the strength of this apparent association.
弯曲杆菌属是大多为自限性小肠结肠炎的常见病因。虽然罕见,但心包炎和心肌心包炎作为弯曲杆菌感染后的并发症越来越多地被记录下来。此类病例主要发生在年轻男性中,且涉及单一病原体,即空肠弯曲菌。我们报告首例结肠弯曲菌小肠结肠炎后发生的心肌心包炎病例,患者为一名免疫功能正常的中年女性。
一名51岁女性因胸痛3天入住心内科。该女性无重大病史或心脏病危险因素,也未报告近期有海外旅行史。在胸痛开始前4天,该女性报告出现急性胃肠道疾病,每天排3 - 4次稀便,就诊时这种情况仍持续。体格检查显示该女性生命体征基本稳定,不过注意到她有轻度心动过速。实验室检查显示C反应蛋白轻度升高,肌钙蛋白I升高,而血清肌酐激酶未升高。心电图(ECG)显示ST段呈凹面抬高,aVR导联PR段抬高,II导联压低。经胸超声心动图(TTE)显示双心室大小和功能正常,无明显瓣膜异常。无左心室节段性室壁运动异常。无心包积液,但心包回声增强。根据胸痛、典型的心电图改变和肌钙蛋白升高,诊断为心肌心包炎。胸痛缓解,经2天观察后出院,但仍有腹泻。出院后,入院时采集的粪便样本培养出弯曲杆菌属。基质辅助激光解吸电离飞行时间质谱(布鲁克)确认培养分离株为结肠弯曲菌。
我们报告首例与先前结肠弯曲菌小肠结肠炎可能相关的心肌心包炎病例。虽然罕见,但心肌心包炎越来越被视为弯曲杆菌感染后的并发症。我们的报告强调了除空肠弯曲菌外其他弯曲杆菌导致心包疾病的可能性。然而,发病机制尚不确定,且缺乏人群水平的数据,这继续限制了关于这种明显关联强度的结论。