炎症性肠病, 新生儿,克罗恩病,溃疡性结肠炎,基因检测," /> 炎症性肠病, 新生儿,克罗恩病,溃疡性结肠炎,基因检测,"/> Inflammatory bowel disease, Neonates, Crohn's disease, Ulcerative colitis,Genetic testing,"/> <span style="font-size:14px;line-height:2;">新生儿炎症性肠病的临床特征及基因诊断</span><span style="font-size:14px;line-height:2;">研究</span><span style="font-size:14px;line-height:2;"></span>
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发育医学电子杂志  2021, Vol. 9 Issue (2): 133-138    DOI: 10.3969/j.issn.2095-5340.2021.02.009
  围产医学   论著 |新生儿 |
新生儿炎症性肠病的临床特征及基因诊断研究
韩涛 张艳平 朱丽敏 安然 杨浪 孔祥永
1. 解放军总医院儿科医学部 解放军总医院第七医学中心八一儿童医院 新生儿科,北京 100700;2. 解
放军总医院第七医学中心 病理科,北京 100700;3. 解放军总医院第七医学中心 消化内镜中心,北京 100700)
Research of the clinical features and gene diagnosis in neonates with inflammatory bowel disease
Han Tao, Zhang Yanping, Zhu Limin, et al
1.Department ofNeonatology, Bayi Children's Hospital, Seventh Medical Center of PLA General Hospital, Beijing 100700,China; 2.Department of Pathology, Seventh Medical Center of PLA General Hospital, Beijing 100700, China;3.Digestive Endoscopy Center, Seventh Medical Center of PLA General Hospital, Department of Pediatrics,Chinese PLA General Hospital, Beijing 100700, China
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摘要 【摘要】 目的  分析2 例新生儿期起病的炎症性肠病临床特点及基因诊断结果,以提高对该病的认识
和临床诊疗水平。 方法 2018 年至2019 年,解放军总医院第七医学中心八一儿童医院共收治2 例新
生儿期起病的炎症性肠病患儿。对2 例诊断为新生儿炎症性肠病的患儿行结肠镜检查,并行病理活检,
采用直接测序法对患儿进行白细胞介素-10 受体A(interleukin-10 receptor A, IL-10RA)基因突变检测。
同时在万方医学网、中国知网、PubMed 等数据库中组合检索相关文献并分析。 结果  ①例1 患儿女
孩,生后以发热、腹泻起病,多发口腔溃疡, C 反应蛋白反复升高,抗感染治疗无效,行肠镜检查提示结
肠多发糜烂溃疡,全外显子基因测序分析结果提示,基因IL-10RA 存在一处纯合突变。抗炎治疗效果不
理想,放弃治疗后死亡。例2 患儿男孩,患儿生后反复腹泻,伴有发热,入院第16 天行结肠镜检查提示
结肠多发溃疡,病理检查提示大肠黏膜组织中度慢性炎伴轻- 中度急性炎及局部糜烂。诊断炎症性肠病,
予抗炎治疗后,患儿病情好转出院。②文献复习:经查阅文献,中文文献数据库检索出新生儿炎性肠病
文献10 篇,PubMed 检索出4 篇。国内文献多以病例报道为主。新生儿炎症性肠病以发热、腹泻为特
征,常见口腔溃疡和肛周病变。血清自身抗体检测阳性率低,药物治疗效果欠佳。基因检测可存在IL-
10RA 基因突变。 结论 对于不明原因腹泻,体重增长不满意,尤其是伴有发热、口腔溃疡者,需高度
警惕新生儿期起病的炎症性肠病,应积极行消化内镜及基因检测,以尽早确诊并予规范治疗。

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关键词:  炎症性肠病')" href="#">炎症性肠病  新生儿  克罗恩病  溃疡性结肠炎  基因检测    
Abstract: 【Abstract】 Objective To analyze the clinical characteristics and gene diagnosis of 2 cases of neonatal
onset inflammatory bowel disease (IBD), then to improve the level of clinical diagnosis and treatment.
Methods From 2018 to 2019, two newborns with IBD were diagnosed in Bayi Children's Hospital, Seventh Medical Center of PLA General Hospital. Clinical data were collected, and the clinical characteristics were summarized. Enteroscopy was performed on two newborns, and pathological biopsies were performed. Interleukin-10 receptor A (IL-10RA) gene mutations were detected by direct sequencing. Relevant literatures searched from Wanfang data, China national knowledge infrastructure (CNKI), PubMed and other databases were reviewed and analyzed. Results ①Case 1 was a girl with fever, diarrhea and multiple oral ulcers after birth. C reactive protein increased repeatedly. Anti-infective treatment was ineffective. Enteroscopy was performed. Examination revealed multiple ulcerative ulcers in the colon. Analysis of the whole exon gene sequence revealed that there was a homozygous mutation in the IL-10RA gene. The anti-inflammatory treatment effect was not satisfactory, and she died after giving up the treatment. Case 2 was a boy with diarrhea and fever. Enteroscopy was performed on the 16th day of admission, and revealed multiple colonic ulcers. Pathological examination revealed moderate chronic inflammation of the colonic mucosal tissue with mild-moderate acute inflammation and local erosion. After being diagnosed as neonatal IBD, and received anti-inflammatory treatment, he improved and was discharged. ②Literatures review: after being reviewed, 10 literatures on neonatal IBD were retrieved from the Chinese literature database, and 4 literatures were retrieved from PubMed. Domestic literature was mainly based on case reports. Neonatal IBD was characterized by fever, diarrhea. Oral ulcers and perianal lesions were common. The positive rate of serum autoantibodies was low, and the effect of drug therapy was poor. Genetic testing showed the presence of mutations in the IL-10RA gene. Conclusions For those with unexplained diarrhea and unsatisfactory weight gain, especially those with fever and oral ulcers, they need to be highly vigilant against IBD that develops during the neonatal period. Active digestive endoscopy and genetic testing should be performed to confirm the diagnosis as soon as possible, and early standard treatment is needed.

Key words:  Inflammatory bowel disease')" href="#">Inflammatory bowel disease    Neonates    Crohn's disease    Ulcerative colitis    Genetic testing
收稿日期:  2020-07-13                     发布日期:  2021-04-01     
基金资助: 全军计划生育专项课题(20JSZ16)
通讯作者:  孔祥永    E-mail:  sdkongxy@126.com
引用本文:    
韩涛 张艳平 朱丽敏 安然 杨浪 孔祥永. 新生儿炎症性肠病的临床特征及基因诊断研究[J]. 发育医学电子杂志, 2021, 9(2): 133-138.
Han Tao, Zhang Yanping, Zhu Limin, et al. Research of the clinical features and gene diagnosis in neonates with inflammatory bowel disease. Journal of Developmental Medicine(Electronic Version), 2021, 9(2): 133-138.
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http://www.fyyxzz.com/CN/10.3969/j.issn.2095-5340.2021.02.009  或          http://www.fyyxzz.com/CN/Y2021/V9/I2/133
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[1] Professional Committee of Respiratory, Society of Neonatologist, Chinese Medical Doctor Association. Clinical application recommendations for heated humidified high flow nasal cannula[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 132 -135 .
[2] HUANG Liu-ming. Development status of precision minimally invasive technique of pediatric surgery[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(3): 190 -192 .
[3] FU Shu-xin, LI Na, LUO Chen. Analysis for symptoms of perimenopause and related factors[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(2): 78 -82 .
[4] NIU Huan-hong. Clinical study for 89 cases of children poisoning[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(2): 102 -104 .
[5] LIAO De-hua, SONG Xiao-lei, XIE Mei-qing . Uterine arteriovenous malformation: a case report and review of the literatures[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(2): 105 -109 .
[6] ZHU Jing-wen, ZHANG Xue-feng. TypeⅡ Crigler-Najjar syndrome: a case report[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(2): 112 -113 .
[7] YU Ruo -han, SUN Lin, LIU Xiang-yuan. Research progress for obstetric antiphospholipid syndrome and recurrent pregnancy loss[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(2): 122 -125 .
[8] Neonatologist Association, Chinese Medical Doctor Association. Consensus guidelines for neonatal transfer (2017) [J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(4): 193 -197 .
[9] ZHANG Guo-cheng. Pay attention to the influence on growth and development of children with chronic disease[J]. Journal of Developmental Medicine(Electronic Version), 2017, 5(4): 198 -201 .
[10] MA Xiu-wei, WEN Xiu-fang, GU Rui-jie, et al. Clinical and electroencephalogram characteristics ofAngelman syndrome in infancy [J]. Journal of Developmental Medicine(Electronic Version), 2016, 4(4): 223 -229 .
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