Ali-Khan Z, Seemayer T A
Trans R Soc Trop Med Hyg. 1975;69(5-6):473-6. doi: 10.1016/0035-9203(75)90101-7.
A 58 year old Chinese male, one week after arriving in Canada from Hong Kong, presented with acute abdominal pain and diarrhoea which was rapidly followed by Escherichia coli infection causing septicaemia and meningitis. His past history revealed bronchial asthma for 15 years treated with steroids. At laparotomy, 7 days after the onset of symptoms, he was found to have extensive haemorrhagic infarction of the small bowel and right colon. Examination of the fibrosed mesenteric vessels revealed numerous filariform larvae of Strongyloides stercoralis, within the walls, and in all layers of bowel wall. The role of the parasite in the production of obliterative arteritis in this fatal case of haemorrhagic enteropathy is discussed. Clinical strongyloidiasis, in uncomplicated cases, varies from mild to severe with gastroenteritis, nausea, colicky abdominal pain, electrolyte imbalance and symptoms of malabsorption syndrome (MARCIAL-ROJAS, 1971). In malnourished individuals and patients with debilitating infections, either newly acquired or asymptomatic latent infection with S. stercoralis can assume severe dimensions (BROWN and PERNA, 1958; HUGHTON and HORN, 1959). Similarly, in patients on steroid (CRUZ et al., 1966; WILLIS and MWOKOLO, 1966; NEEFE et al., 1973) and immunosuppressive therapy for lymphomatous diseases or deficient in immune response (ROGERS and NELSON, 1966; RIVERA et al., 1970), systemic strongyloidiasis is often fatal. The increased frequency of auto-infection in such patients with a breached immune barrier is, however, unclear. Further complications of this infection due to severe enterocolitis result in sepsis, bacteraemia and meningitis (BROWN and PERNA, 1958; HUGHTON and HORN, 1959). This paper presents a fatal case of S. stercoralis infection which illustrates an uncommon if not unique, mechanism in its production of haemorrhagic enteropathy leading to sepsis and death.
一名58岁的中国男性,从香港抵达加拿大一周后,出现急性腹痛和腹泻,随后迅速发生大肠杆菌感染,导致败血症和脑膜炎。他的既往病史显示有15年支气管哮喘病史,一直用类固醇治疗。症状出现7天后进行剖腹手术,发现他的小肠和右结肠有广泛的出血性梗死。对纤维化的肠系膜血管进行检查发现,肠壁各层内有大量粪类圆线虫丝状幼虫。本文讨论了在这例致命的出血性肠病中,寄生虫在闭塞性动脉炎形成中的作用。临床粪类圆线虫病,在无并发症的情况下,从轻度到重度不等,表现为肠胃炎、恶心、绞痛性腹痛、电解质失衡和吸收不良综合征症状(马尔西亚尔 - 罗哈斯,1971年)。在营养不良的个体以及患有使人衰弱的感染(无论是新获得的感染还是无症状的潜伏感染)的患者中,粪类圆线虫感染都可能发展为严重疾病(布朗和佩尔纳,1958年;休顿和霍恩,1959年)。同样,在接受类固醇治疗(克鲁兹等人,1966年;威利斯和姆沃科洛,1966年;尼费等人,1973年)以及因淋巴瘤疾病接受免疫抑制治疗或免疫反应缺陷(罗杰斯和尼尔森,1966年;里韦拉等人,1970年)的患者中,全身性粪类圆线虫病往往是致命的。然而,在这些免疫屏障受损的患者中,自身感染频率增加的原因尚不清楚。这种感染由于严重的小肠结肠炎进一步引发败血症、菌血症和脑膜炎(布朗和佩尔纳,1958年;休顿和霍恩,1959年)。本文报告了一例致命的粪类圆线虫感染病例,该病例说明了其导致出血性肠病并进而导致败血症和死亡的一种虽不常见但也并非独一无二的机制。