与COVID-19相关的儿童多系统炎症综合征(MIS-C)的儿科胃肠道疾病:一个病例系列

IF 0.5 Q4 PEDIATRICS
Case Reports in Pediatrics Pub Date : 2025-09-03 eCollection Date: 2025-01-01 DOI:10.1155/crpe/8815325
Michele di Toma, Ilaria Cassitti, Benedetta Ciccone, Enrica Manca, Alessandra Marinari, Isabella Patisso, Maria Nobili, Angelo Campanozzi
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引用次数: 0

摘要

儿童多系统炎症综合征(MIS-C)是一种与既往SARS-CoV-2感染相关的免疫激活综合征。SARS-CoV-2感染后2-6周出现临床表现,可能累及心、肺、肾、皮肤、中枢神经系统和消化道。我院于2021年1月至2022年3月收治5例misc患儿(6.6±1.3岁,M:F = 3:2)。患者均有胃肠道表现,SARS-CoV-2分子拭子阴性,血清学阳性。据报告,一名儿童此前已知无症状SARS-CoV-2感染(入院前4周以上)。另有1例报告接种了COVID-19疫苗(入院前4周第二次接种)。3 /5为肥胖儿童(BMI大于95百分位)。所有患者均出现发热、腹痛和食欲不振。4 /5出现呕吐,3/5出现腹泻,2/5出现便秘,2名男性患者出现阴囊水肿。3 /5表现为严重的胃肠道受累,类似阑尾病变;其中1例行腹腔镜探查,无阑尾炎组织学表现。他们都没有转氨酶水平升高,但有一个孩子表现出胰腺炎。IL-6中位峰值186.5 pg/mL(范围:15.1 ~ 692.5,正常值:0.5 ~ 6.4);CRP 191.4 mg/L(范围:131 ~ 386.7,正常值:0 ~ 2);降钙素原19.8 ng/mL(范围4.27 ~ 100,正常值< 0.5)。我们用静脉注射免疫球蛋白和类固醇治疗所有患者。一名患者需要吸氧和肠外营养。没有人死亡。根据已发表的数据,misc患者出现腹部症状的比例很高。所有病例均有发热和胃肠道症状,其中一些类似急性阑尾炎。在文献中,大多数因怀疑阑尾炎入院的患者都进行了阑尾切除术。此外,组织病理学显示只有浆膜炎症,没有急性阑尾炎的典型累及。在诊断为misc后,开始了特异性治疗,导致临床改善。总之,在2019冠状病毒病大流行期间,对于出现持续发热和严重胃肠道症状的儿童,应始终考虑misc,以避免不必要的手术探查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pediatric Gastrointestinal Disorders in Multisystem Inflammatory Syndrome in Children (MIS-C) Associated With COVID-19: A Case Series.

Multisystem inflammatory syndrome in children (MIS-C) is an immune activation syndrome associated with prior SARS-CoV-2 infection. Clinical manifestations of MIS-C develop 2-6 weeks after SARS-CoV-2 infection with possible involvement of the heart, lungs, kidneys, skin, central nervous system, and digestive tract. Five children with MIS-C (6.6 ± 1.3 years, M:F = 3:2) were admitted to our hospital from January 2021 to March 2022. They all presented with gastrointestinal manifestations, with SARS-CoV-2 molecular swab negativity and positive serology. One child was reported to have a known previous asymptomatic SARS-CoV-2 infection (more than 4 weeks prior to admission). Another one was reported to have received COVID-19 vaccine (second dose four weeks prior to admission). Three/5 were obese children (BMI greater than 95th percentile). All patients experienced fever, abdominal pain, and lack of appetite. Four/5 had vomiting, 3/5 presented diarrhea, 2/5 had constipation, and two male patients had scrotal edema. Three/5 presented with severe gastrointestinal involvement, mimicking appendicopathy; one of them underwent exploratory laparoscopy without histological features of appendicitis. None of them had increased levels of transaminases but one child showed pancreatitis. The median peak value of: IL-6 was 186.5 pg/mL (range: 15.1-692.5; normal values: 0.5-6.4); CRP was 191.4 mg/L (range: 131-386.7; normal values: 0-2); procalcitonin was 19.8 ng/mL (range: 4.27-100; normal value: < 0.5). We treated all patients with intravenous immunoglobulins and steroids. One patient needed oxygen therapy and parenteral nutrition. Nobody died. According to published data, patients with MIS-C have a high rate of abdominal symptoms. Fever and gastrointestinal symptoms were reported in all cases, some of them mimicking acute appendicitis. In the literature, appendectomy was performed in the majority of patients admitted as suspected appendicitis. Moreover, histopathology demonstrated only serosal inflammation, without the typical involvement of acute appendicitis. Following the diagnosis of MIS-C, specific therapy was started, leading to clinical improvement. In conclusion, during the COVID-19 pandemic, MIS-C should always be taken into account in children with persistent fever and severe gastrointestinal symptoms to avoid unnecessary surgical exploration.

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