North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition Position Paper on the Evaluation and Management for Patients With Very Early-onset Inflammatory Bowel Disease

被引:65
|
作者
Kelsen, Judith R. [1 ]
Sullivan, Kathleen E. [2 ]
Rabizadeh, Shervin [3 ]
Singh, Namita [4 ]
Snapper, Scott [5 ,6 ,7 ]
Elkadri, Abdul [8 ]
Grossman, Andrew B. [1 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Perelman Sch Med, Div Gastroenterol Hepatol & Nutr, Philadelphia, PA 19104 USA
[2] Univ Penn, Childrens Hosp Philadelphia, Perelman Sch Med, Div Immunol & Allergy, Philadelphia, PA 19104 USA
[3] Cedar Sinai Med Ctr, Div Gastroenterol Hepatol & Nutr, Los Angeles, CA USA
[4] Univ Washington, Seattle Childrens Hosp, Dept Pediat, Div Gastroenterol, Seattle, WA 98195 USA
[5] Harvard Med Sch, Boston Childrens Hosp, Dept Pediat, Div Gastroenterol Hepatol & Nutr, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Dept Med, Div Gastroenterol, 75 Francis St, Boston, MA 02115 USA
[7] Harvard Med Sch, Boston, MA 02115 USA
[8] Med Coll Wisconsin, Div Gastroenterol Hepatol & Nutr, Milwaukee, WI 53226 USA
关键词
Crohn disease; ulcerative colitis; very early-onset inflammatory bowel disease; CHRONIC GRANULOMATOUS-DISEASE; HERMANSKY-PUDLAK-SYNDROME; MEVALONATE KINASE-DEFICIENCY; X-LINKED AGAMMAGLOBULINEMIA; EXOME SEQUENCING ANALYSIS; REGULATORY T-CELLS; CROHNS-DISEASE; IMMUNE DYSREGULATION; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; INTESTINAL INFLAMMATION;
D O I
10.1097/MPG.0000000000002567
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The rate of pediatric inflammatory bowel disease (IBD) has been increasing over the last decade and this increase has occurred most rapidly in the youngest children diagnosed <6 years, known as very early-onset inflammatory bowel disease (VEO-IBD). These children can present with more extensive and severe disease than older children and adults. The contribution of host genetics in this population is underscored by the young age of onset and the distinct, aggressive phenotype. In fact, monogenic defects, often involving primary immunodeficiency genes, have been identified in children with VEO-IBD and have led to targeted and life-saving therapy. This position paper will discuss the phenotype of VEO-IBD and outline the approach and evaluation for these children and what factors should trigger concern for an underlying immunodeficiency. We will then review the immunological assays and genetic studies that can facilitate the identification of the underlying diagnosis in patients with VEO-IBD and how this evaluation may lead to directed therapies. The position paper will also aid the pediatric gastroenterologist in recognizing when a patient should be referred to a center specializing in the care of these patients. These guidelines are intended for pediatricians, allied health professionals caring for children, pediatric gastroenterologists, pediatric pathologists, and immunologists.
引用
收藏
页码:389 / 403
页数:15
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