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Primary Immunodeficiencies in Children Initially Admitted with Gastrointestinal/Liver Manifestations
The gastrointestinal system is the most commonly affected organ, followed by the lungs, in patients with primary immunodeficiency disease (PID). Hence, it is common for children with PIDs to present with gastrointestinal symptoms. We aimed to analyze the clinical and histopathological findings of pa...
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Published in: | Pediatric gastroenterology, hepatology & nutrition 2023, Hepatology & Nutrition, 26(4), , pp.201-212 |
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container_title | Pediatric gastroenterology, hepatology & nutrition |
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creator | Cakir, Murat Yakici, Nalan Sag, Elif Kaya, Gulay Bahadir, Ayşenur Cebi, Alper Han Orhan, Fazil |
description | The gastrointestinal system is the most commonly affected organ, followed by the lungs, in patients with primary immunodeficiency disease (PID). Hence, it is common for children with PIDs to present with gastrointestinal symptoms. We aimed to analyze the clinical and histopathological findings of patients who were initially admitted to pediatric gastroenterology/hepatology clinics and subsequently diagnosed with PIDs to identify the clinical clues for PIDs.
The demographic, laboratory, and histopathological findings, treatment modality, and outcomes of patients initially admitted to the pediatric gastroenterology/hepatology unit and subsequently diagnosed with PIDs were recorded.
The study included 24 patients (58.3% male; median age [range]: 29 [0.5-204] months). Common clinical presentations included chronic diarrhea (n=8), colitis (n=6), acute hepatitis (n=4), and acute liver failure (n=2). The association of autoimmune diseases, development of malignant diseases, and severe progression of viral diseases was observed in 20.8%, 8.3%, and 16.6% of the patients, respectively. Antibody deficiency was predominantly diagnosed in 29.2% of patients, combined immunodeficiency in 20.8%, immune dysregulation in 12.5%, defects in intrinsic and innate immunity in 4.2%, autoinflammatory disorders in 8.3%, and congenital defects of phagocytes in 4.2%. Five patients remained unclassified (20.8%).
Patients with PIDs may initially experience gastrointestinal or liver problems. It is recommended that the association of autoimmune or malignant diseases or severe progression of viral diseases provide pediatric gastroenterologists some suspicion of PIDs. After screening using basic laboratory tests, genetic analysis is mandatory for a definitive diagnosis. |
doi_str_mv | 10.5223/pghn.2023.26.4.201 |
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The demographic, laboratory, and histopathological findings, treatment modality, and outcomes of patients initially admitted to the pediatric gastroenterology/hepatology unit and subsequently diagnosed with PIDs were recorded.
The study included 24 patients (58.3% male; median age [range]: 29 [0.5-204] months). Common clinical presentations included chronic diarrhea (n=8), colitis (n=6), acute hepatitis (n=4), and acute liver failure (n=2). The association of autoimmune diseases, development of malignant diseases, and severe progression of viral diseases was observed in 20.8%, 8.3%, and 16.6% of the patients, respectively. Antibody deficiency was predominantly diagnosed in 29.2% of patients, combined immunodeficiency in 20.8%, immune dysregulation in 12.5%, defects in intrinsic and innate immunity in 4.2%, autoinflammatory disorders in 8.3%, and congenital defects of phagocytes in 4.2%. Five patients remained unclassified (20.8%).
Patients with PIDs may initially experience gastrointestinal or liver problems. It is recommended that the association of autoimmune or malignant diseases or severe progression of viral diseases provide pediatric gastroenterologists some suspicion of PIDs. After screening using basic laboratory tests, genetic analysis is mandatory for a definitive diagnosis.</description><identifier>ISSN: 2234-8646</identifier><identifier>EISSN: 2234-8840</identifier><identifier>DOI: 10.5223/pghn.2023.26.4.201</identifier><identifier>PMID: 37485029</identifier><language>eng</language><publisher>Korea (South): The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition</publisher><subject>Original ; 소아과학</subject><ispartof>Pediatric Gastroenterology, 2023, Hepatology & Nutrition, 26(4), , pp.201-212</ispartof><rights>Copyright © 2023 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition.</rights><rights>Copyright © 2023 by The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2023 The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c389t-3d58d61630cc7ca960594c06975b6f291a9e7b328a850a01274c67b3ec2691ac3</cites><orcidid>0000-0003-0738-4679 ; 0000-0003-4071-6129 ; 0000-0002-4850-932X ; 0000-0002-0713-5122 ; 0000-0003-3069-2872 ; 0000-0001-9226-369X ; 0000-0001-7388-874X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356973/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356973/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37485029$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002980200$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Cakir, Murat</creatorcontrib><creatorcontrib>Yakici, Nalan</creatorcontrib><creatorcontrib>Sag, Elif</creatorcontrib><creatorcontrib>Kaya, Gulay</creatorcontrib><creatorcontrib>Bahadir, Ayşenur</creatorcontrib><creatorcontrib>Cebi, Alper Han</creatorcontrib><creatorcontrib>Orhan, Fazil</creatorcontrib><title>Primary Immunodeficiencies in Children Initially Admitted with Gastrointestinal/Liver Manifestations</title><title>Pediatric gastroenterology, hepatology & nutrition</title><addtitle>Pediatr Gastroenterol Hepatol Nutr</addtitle><description>The gastrointestinal system is the most commonly affected organ, followed by the lungs, in patients with primary immunodeficiency disease (PID). Hence, it is common for children with PIDs to present with gastrointestinal symptoms. We aimed to analyze the clinical and histopathological findings of patients who were initially admitted to pediatric gastroenterology/hepatology clinics and subsequently diagnosed with PIDs to identify the clinical clues for PIDs.
The demographic, laboratory, and histopathological findings, treatment modality, and outcomes of patients initially admitted to the pediatric gastroenterology/hepatology unit and subsequently diagnosed with PIDs were recorded.
The study included 24 patients (58.3% male; median age [range]: 29 [0.5-204] months). Common clinical presentations included chronic diarrhea (n=8), colitis (n=6), acute hepatitis (n=4), and acute liver failure (n=2). The association of autoimmune diseases, development of malignant diseases, and severe progression of viral diseases was observed in 20.8%, 8.3%, and 16.6% of the patients, respectively. Antibody deficiency was predominantly diagnosed in 29.2% of patients, combined immunodeficiency in 20.8%, immune dysregulation in 12.5%, defects in intrinsic and innate immunity in 4.2%, autoinflammatory disorders in 8.3%, and congenital defects of phagocytes in 4.2%. Five patients remained unclassified (20.8%).
Patients with PIDs may initially experience gastrointestinal or liver problems. It is recommended that the association of autoimmune or malignant diseases or severe progression of viral diseases provide pediatric gastroenterologists some suspicion of PIDs. After screening using basic laboratory tests, genetic analysis is mandatory for a definitive diagnosis.</description><subject>Original</subject><subject>소아과학</subject><issn>2234-8646</issn><issn>2234-8840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpVUdtKAzEQDaLYov0BH2QfRWjNbbObJynFS6GiiD6HNJttR3ezNUkr_r2pVdFAmGHmzJmTHIROCB7llLKL1WLpRhRTNqJixFNG9lA_NfiwLDne_8kFFz00COEFp1MQxgg5RD1W8DLHVPZR9eCh1f4jm7bt2nWVrcGAdemGDFw2WUJTeeuyqYMIumk-snHVQoy2yt4hLrMbHaLvwEUbIjjdXMxgY312px3UqaQjdC4co4NaN8EOvuMRer6-eprcDmf3N9PJeDY0rJRxyKq8rAQRDBtTGC0FziU3WMgin4uaSqKlLeaMljqJ15jQghuRCtZQkZqGHaHzHa_ztXo1oDoNX3HRqVevxo9PU0UwLZgkJIEvd-DVet7aylgXvW7UavcfX6P_Ow6WiWiTGFieNLHEcPbN4Lu3dXqtaiEY2zTa2W4dFC054ZhhIhOU7qDGdyF4W__uIVht_VRbP9XWT0WF4inbKjz9q_B35Mc99gnvL53Z</recordid><startdate>20230701</startdate><enddate>20230701</enddate><creator>Cakir, Murat</creator><creator>Yakici, Nalan</creator><creator>Sag, Elif</creator><creator>Kaya, Gulay</creator><creator>Bahadir, Ayşenur</creator><creator>Cebi, Alper Han</creator><creator>Orhan, Fazil</creator><general>The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition</general><general>대한소아소화기영양학회</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0003-0738-4679</orcidid><orcidid>https://orcid.org/0000-0003-4071-6129</orcidid><orcidid>https://orcid.org/0000-0002-4850-932X</orcidid><orcidid>https://orcid.org/0000-0002-0713-5122</orcidid><orcidid>https://orcid.org/0000-0003-3069-2872</orcidid><orcidid>https://orcid.org/0000-0001-9226-369X</orcidid><orcidid>https://orcid.org/0000-0001-7388-874X</orcidid></search><sort><creationdate>20230701</creationdate><title>Primary Immunodeficiencies in Children Initially Admitted with Gastrointestinal/Liver Manifestations</title><author>Cakir, Murat ; Yakici, Nalan ; Sag, Elif ; Kaya, Gulay ; Bahadir, Ayşenur ; Cebi, Alper Han ; Orhan, Fazil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-3d58d61630cc7ca960594c06975b6f291a9e7b328a850a01274c67b3ec2691ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Original</topic><topic>소아과학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cakir, Murat</creatorcontrib><creatorcontrib>Yakici, Nalan</creatorcontrib><creatorcontrib>Sag, Elif</creatorcontrib><creatorcontrib>Kaya, Gulay</creatorcontrib><creatorcontrib>Bahadir, Ayşenur</creatorcontrib><creatorcontrib>Cebi, Alper Han</creatorcontrib><creatorcontrib>Orhan, Fazil</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Pediatric gastroenterology, hepatology & nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cakir, Murat</au><au>Yakici, Nalan</au><au>Sag, Elif</au><au>Kaya, Gulay</au><au>Bahadir, Ayşenur</au><au>Cebi, Alper Han</au><au>Orhan, Fazil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary Immunodeficiencies in Children Initially Admitted with Gastrointestinal/Liver Manifestations</atitle><jtitle>Pediatric gastroenterology, hepatology & nutrition</jtitle><addtitle>Pediatr Gastroenterol Hepatol Nutr</addtitle><date>2023-07-01</date><risdate>2023</risdate><volume>26</volume><issue>4</issue><spage>201</spage><epage>212</epage><pages>201-212</pages><issn>2234-8646</issn><eissn>2234-8840</eissn><abstract>The gastrointestinal system is the most commonly affected organ, followed by the lungs, in patients with primary immunodeficiency disease (PID). Hence, it is common for children with PIDs to present with gastrointestinal symptoms. We aimed to analyze the clinical and histopathological findings of patients who were initially admitted to pediatric gastroenterology/hepatology clinics and subsequently diagnosed with PIDs to identify the clinical clues for PIDs.
The demographic, laboratory, and histopathological findings, treatment modality, and outcomes of patients initially admitted to the pediatric gastroenterology/hepatology unit and subsequently diagnosed with PIDs were recorded.
The study included 24 patients (58.3% male; median age [range]: 29 [0.5-204] months). Common clinical presentations included chronic diarrhea (n=8), colitis (n=6), acute hepatitis (n=4), and acute liver failure (n=2). The association of autoimmune diseases, development of malignant diseases, and severe progression of viral diseases was observed in 20.8%, 8.3%, and 16.6% of the patients, respectively. Antibody deficiency was predominantly diagnosed in 29.2% of patients, combined immunodeficiency in 20.8%, immune dysregulation in 12.5%, defects in intrinsic and innate immunity in 4.2%, autoinflammatory disorders in 8.3%, and congenital defects of phagocytes in 4.2%. Five patients remained unclassified (20.8%).
Patients with PIDs may initially experience gastrointestinal or liver problems. It is recommended that the association of autoimmune or malignant diseases or severe progression of viral diseases provide pediatric gastroenterologists some suspicion of PIDs. After screening using basic laboratory tests, genetic analysis is mandatory for a definitive diagnosis.</abstract><cop>Korea (South)</cop><pub>The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition</pub><pmid>37485029</pmid><doi>10.5223/pghn.2023.26.4.201</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-0738-4679</orcidid><orcidid>https://orcid.org/0000-0003-4071-6129</orcidid><orcidid>https://orcid.org/0000-0002-4850-932X</orcidid><orcidid>https://orcid.org/0000-0002-0713-5122</orcidid><orcidid>https://orcid.org/0000-0003-3069-2872</orcidid><orcidid>https://orcid.org/0000-0001-9226-369X</orcidid><orcidid>https://orcid.org/0000-0001-7388-874X</orcidid><oa>free_for_read</oa></addata></record> |
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title | Primary Immunodeficiencies in Children Initially Admitted with Gastrointestinal/Liver Manifestations |
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