Needs for Increased Awareness of Gastrointestinal Manifestations in Patients With Human Inborn Errors of Immunity

被引:6
作者
Kim, Eun Sil [1 ]
Kim, Dongsub [1 ,2 ]
Yoon, Yoonsun [1 ,3 ]
Kwon, Yiyoung [1 ]
Park, Sangwoo [1 ]
Kim, Jihyun [1 ]
Ahn, Kang Mo [1 ]
Ahn, Soomin [4 ]
Choe, Yon Ho [1 ]
Kim, Yae-Jean [1 ]
Kim, Mi Jin [1 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Dept Pediat, Sch Med, Seoul, South Korea
[2] Kyungpook Natl Univ, Kyungpook Natl Univ Hosp, Sch Med, Dept Pediat, Daegu, South Korea
[3] Korea Univ, Guro Hosp, Coll Med, Dept Pediat, Seoul, South Korea
[4] Sungkyunkwan Univ, Samsung Med Ctr, Dept Pathol, Sch Med, Seoul, South Korea
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
关键词
inborn errors of immunity; primary immunodeficiencies; gastrointestinal; endoscopy; malignancy; inflammatory bowel disease; PRIMARY IMMUNODEFICIENCY DISEASES; THROMBOCYTOPENIC PURPURA; ULCERATIVE-COLITIS; CANCER; DEFICIENCY; FEATURES; CHILDREN;
D O I
10.3389/fimmu.2021.698721
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gastrointestinal (GI) tract is frequently affected by inborn errors of immunity (IEI), and GI manifestations can be present in IEI patients before a diagnosis is confirmed. We aimed to investigate clinical features, endoscopic and histopathologic findings in IEI patients. This was a retrospective cohort study conducted from 1995 to 2020. Eligible patients were diagnosed with IEI and had GI manifestations that were enough to require endoscopies. IEI was classified according to the International Union of Immunological Societies classification. Of 165 patients with IEI, 55 (33.3%) had GI manifestations, and 19 (11.5%) underwent endoscopy. Among those 19 patients, nine (47.4%) initially presented with GI manifestations. Thirteen patients (68.4%) were male, and the mean age of patients 11.5 +/- 7.9 years (range, 0.6 - 26.6) when they were consulted and evaluated with endoscopy. The most common type of IEI with severe GI symptoms was "Disease of immune dysregulation" (31.6%) followed by "Phagocyte defects" (26.3%), according to the International Union of Immunological Societies classification criteria. Patients had variable GI symptoms such as chronic diarrhea (68.4%), hematochezia (36.8%), abdominal pain (31.6%), perianal disease (10.5%), and recurrent oral ulcers (10.5%). During the follow-up period, three patients developed GI tract neoplasms (early gastric carcinoma, mucosa associated lymphoid tissue lymphoma of colon, and colonic tubular adenoma, 15.8%), and 12 patients (63.2%) were diagnosed with inflammatory bowel disease (IBD)-like colitis. Investigating immunodeficiency in patients with atypical GI symptoms can provide an opportunity for correct diagnosis and appropriate disease-specific therapy. Gastroenterologists and immunologists should consider endoscopy when atypical GI manifestations appear in IEI patients to determine if IBD-like colitis or neoplasms including premalignant and malignant lesions have developed. Also, if physicians in various fields are better educated about IEI-specific complications, early diagnosis and disease-specific treatment for IEI will be made possible.
引用
收藏
页数:11
相关论文
共 41 条
[1]   Gastrointestinal Manifestations and Complications of Primary Immunodeficiency Disorders [J].
Agarwal, Shradha ;
Cunningham-Rundles, Charlotte .
IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA, 2019, 39 (01) :81-+
[2]   Diagnosis and Treatment of Gastrointestinal Disorders in Patients With Primary Immunodeficiency [J].
Agarwal, Shradha ;
Mayer, Lloyd .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2013, 11 (09) :1050-1063
[3]   Gastrointestinal Manifestations in Children with Primary Immunodeficiencies: Single Center: 12 Years Experience [J].
Akkelle, Bilge S. ;
Tutar, Engin ;
Volkan, Burcu ;
Sengul, Ozlem K. ;
Ozen, Ahmet ;
Celikel, Cigdem A. ;
Ertem, Deniz .
DIGESTIVE DISEASES, 2019, 37 (01) :45-52
[4]   Profile of the patients who present to immunology outpatient clinics because of frequent infections [J].
Aldirmaz, Sonay ;
Yucel, Esra ;
Kiykim, Ayca ;
Cokugras, Haluk ;
Akcakaya, Necla ;
Camcioglu, Yildiz .
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, 2014, 49 (03) :210-216
[5]  
Alimchandani M, 2013, AM J SURG PATHOL, V37, P1365, DOI 10.1097/PAS.0b013e318297427d
[6]   Primary immunodeficiency and autoimmunity: A comprehensive review [J].
Amaya-Uribe, Laura ;
Rojas, Manuel ;
Azizi, Gholamreza ;
Anaya, Juan-Manuel ;
Gershwin, M. Eric .
JOURNAL OF AUTOIMMUNITY, 2019, 99 :52-72
[7]   NOD2-associated diseases: Bridging innate immunity and autoinflammation [J].
Borzutzky, Arturo ;
Fried, Ari ;
Chou, Janet ;
Bonilla, Francisco A. ;
Kim, Susan ;
Dedeoglu, Fatma .
CLINICAL IMMUNOLOGY, 2010, 134 (03) :251-261
[8]   Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification [J].
Bousfiha, Aziz ;
Jeddane, Leila ;
Picard, Capucine ;
Al-Herz, Waleed ;
Ailal, Fatima ;
Chatila, Talal ;
Cunningham-Rundles, Charlotte ;
Etzioni, Amos ;
Franco, Jose Luis ;
Holland, Steven M. ;
Klein, Christoph ;
Morio, Tomohiro ;
Ochs, Hans D. ;
Oksenhendler, Eric ;
Puck, Jennifer ;
Torgerson, Troy R. ;
Casanova, Jean-Laurent ;
Sullivan, Kathleen E. ;
Tangye, Stuart G. .
JOURNAL OF CLINICAL IMMUNOLOGY, 2020, 40 (01) :66-81
[9]   Subclinical intestinal inflammation in chronic granulomatous disease patients [J].
Broides, Arnon ;
Sagi, Orli ;
Pinsk, Vered ;
Levy, Jacov ;
Yerushalmi, Baruch .
IMMUNOLOGIC RESEARCH, 2016, 64 (01) :155-159
[10]   Association of glycogen storage disease 1b and Crohn disease: results of a North American survey [J].
Dieckgraefe, BK ;
Korzenik, JR ;
Husain, A ;
Dieruf, L .
EUROPEAN JOURNAL OF PEDIATRICS, 2002, 161 (Suppl 1) :S88-S92