The University of Oklahoma College of Medicine, 800 Stanton L Young Blvd, Oklahoma City, OK, 73117, USA.
Division of Pediatric Surgery, Oklahoma Children's Hospital, 1200 Everett Drive, ET NP 2320, Oklahoma City, OK, 73104, USA.
J Med Case Rep. 2022 Apr 17;16(1):155. doi: 10.1186/s13256-022-03381-z.
Methicillin-resistant Staphylococcus aureus enterocolitis is a rare disease that typically affects immunocompromised adults. Most cases of pediatric enterocolitis are caused by Gram-negative bacteria, Gram-positive Clostridiodes difficile, or viruses. This is the first published case report of a toddler with methicillin-resistant Staphylococcus aureus enterocolitis.
A 16-month-old non-Hispanic White boy with no past medical or psychosocial history initially presented to the emergency room with abdominal pain and emesis. Past family history was pertinent only for his father having a history of constipation. He was diagnosed with intussusception and underwent successful contrast reduction on hospital day 0. The following day, the patient had recurrent symptoms and a repeat contrast enema showed no evidence of recurrent intussusception. A computed tomography scan was obtained, which was concerning for possible recurrence with compromised bowel. He was taken to the operating room for operative reduction and underwent an ileocecetomy with primary handsewn end-to-end anastomosis. His postoperative course was complicated by an anastomotic leak on hospital day 6 necessitating reoperation and creation of an end ileostomy with mucous fistula. He received intravenous metronidazole, ceftriaxone, and ceftazidime antibiotics during his hospital course. On postoperative day 12, the patient developed a sudden increase in ileostomy output, and stool cultures were obtained. His symptoms persisted despite diet modifications, stopping antibiotics, and initiating loperamide. Three days later, stool cultures resulted negative for Escherichia coli, Salmonella, Shigella, Campylobacter species, and Clostridiodes difficile but were positive for methicillin-resistant Staphylococcus aureus. The patient was started on a 10-day course of oral vancomycin and discharged home in good condition 4 days later. After 12 weeks, the patient underwent reversal of the ostomy and is doing well at the 1 month postoperative follow-up, now 5 months from his initial surgery.
To our knowledge, this is the first published report of a toddler being diagnosed with methicillin-resistant Staphylococcus aureus enterocolitis. Because methicillin-resistant Staphylococcus aureus enterocolitis is rare and has overlapping symptoms with more common gastrointestinal pathologies, it is often misdiagnosed. When a patient presents with diarrhea or high ostomy output along with fecal cultures negative for Clostridiodes difficile and other common pathogenic agents, methicillin-resistant Staphylococcus aureus should be considered.
耐甲氧西林金黄色葡萄球菌性肠炎是一种罕见疾病,通常影响免疫功能低下的成年人。大多数小儿肠炎是由革兰氏阴性菌、革兰氏阳性艰难梭菌或病毒引起的。这是首例经文献报道的耐甲氧西林金黄色葡萄球菌性肠炎幼儿病例。
一名 16 个月大的非西班牙裔白人男孩,既往无医疗或精神社会史,最初因腹痛和呕吐到急诊就诊。仅其父亲有便秘病史的家族史与此相关。他被诊断为肠套叠,并在入院第 0 天成功进行了对比剂复位。次日,患儿出现复发症状,再次进行对比灌肠检查未见肠套叠复发证据。进行了 CT 扫描,提示可能存在复发性肠套叠和肠壁受损。他被送入手术室进行手术复位,并进行回盲肠切除术和一期手工端端吻合术。术后患儿出现吻合口漏,第 6 天需要再次手术,行回肠造口术并形成带有黏膜瘘的末端回肠造口。他在住院期间接受了甲硝唑、头孢曲松和头孢他啶静脉抗生素治疗。术后第 12 天,患儿出现回肠造口输出量突然增加,采集了粪便培养。尽管进行了饮食调整、停止使用抗生素和开始使用洛哌丁胺,但其症状仍持续存在。3 天后,粪便培养结果为阴性,未检出大肠杆菌、沙门氏菌、志贺氏菌、弯曲杆菌和艰难梭菌,但耐甲氧西林金黄色葡萄球菌阳性。患儿开始接受 10 天疗程的口服万古霉素治疗,4 天后出院情况良好。12 周后,患儿进行了造口逆转,在术后 1 个月随访时情况良好,距最初手术已过去 5 个月。
据我们所知,这是首例经文献报道的幼儿确诊耐甲氧西林金黄色葡萄球菌性肠炎的病例。由于耐甲氧西林金黄色葡萄球菌性肠炎罕见,且与更常见的胃肠道疾病具有重叠症状,因此常被误诊。当患者出现腹泻或高造口输出量,粪便培养艰难梭菌及其他常见病原体均为阴性时,应考虑耐甲氧西林金黄色葡萄球菌感染。