Microscopic Colitis in Children With Chronic Diarrhea

ABSTRACT Objective: The aim of the present study was to study microscopic colitis (MC) in children with special reference to its role in chronic diarrhea and changes in mucosal biopsies. Methods: A total of 100 consecutive children ages 3 to 12 years, with nonbloody diarrhea (passage of ≥3 loose sto...

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Veröffentlicht in:Journal of pediatric gastroenterology and nutrition 2013-08, Vol.57 (2), p.240-244
Hauptverfasser: Singh, Prashant, Das, Prasenjit, Jain, A.K., Mathan, Minnie, Mathur, Meera, Bhat, Abdus Sami, Varma, Sharat, Chaturvedi, Mona K., Gupta, Siddhartha Datta, Bhatnagar, Shinjini
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container_end_page 244
container_issue 2
container_start_page 240
container_title Journal of pediatric gastroenterology and nutrition
container_volume 57
creator Singh, Prashant
Das, Prasenjit
Jain, A.K.
Mathan, Minnie
Mathur, Meera
Bhat, Abdus Sami
Varma, Sharat
Chaturvedi, Mona K.
Gupta, Siddhartha Datta
Bhatnagar, Shinjini
description ABSTRACT Objective: The aim of the present study was to study microscopic colitis (MC) in children with special reference to its role in chronic diarrhea and changes in mucosal biopsies. Methods: A total of 100 consecutive children ages 3 to 12 years, with nonbloody diarrhea (passage of ≥3 loose stools per day) of >12 weeks' duration were screened and 26 were enrolled in the study in which no specific etiology could be found and colonoscopy did not reveal any mucosal abnormality. Colonic biopsies were evaluated for the presence of lymphocytic colitis or collagenous colitis and those with the characteristic changes were defined to have MC (group A). Colonic biopsies from patients with MC were compared with biopsies from patients with chronic diarrhea but no evidence of MC (group B). One hundred children ages 3 to 12 years with bleeding per rectum were screened and colonic biopsies from 45 patients (group C) who had colonic mucosal changes but no vascular or polyp lesion were compared with patients with MC. Results: Of the 26 patients with chronic diarrhea, MC was found in 5 (3 lymphocytic colitis and 2 collagenous colitis). Significantly higher polymorphonuclear infiltration was seen in group A as compared with group B (13.8 [5.4–20.6] vs 7.2 [0–19.6]; P = 0.03) or group C (13.8 [5.4–20.6] vs 4 [0–13.4]; P = 0.007). Intraepithelial lymphocytes (12 [4–32] vs 4 [0–24]; P = 0.008) and basement membrane thickening (3.5 [2.9–10.6] vs 2.5 [1.6–5.86]; P = 0.008) were also significantly higher in group A as compared with group C. Conclusions: MC was found to be present in children with nonbloody chronic diarrhea in children. Further multicentric studies may provide adequate data on its prevalence.
doi_str_mv 10.1097/MPG.0b013e3182942868
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Methods: A total of 100 consecutive children ages 3 to 12 years, with nonbloody diarrhea (passage of ≥3 loose stools per day) of &gt;12 weeks' duration were screened and 26 were enrolled in the study in which no specific etiology could be found and colonoscopy did not reveal any mucosal abnormality. Colonic biopsies were evaluated for the presence of lymphocytic colitis or collagenous colitis and those with the characteristic changes were defined to have MC (group A). Colonic biopsies from patients with MC were compared with biopsies from patients with chronic diarrhea but no evidence of MC (group B). One hundred children ages 3 to 12 years with bleeding per rectum were screened and colonic biopsies from 45 patients (group C) who had colonic mucosal changes but no vascular or polyp lesion were compared with patients with MC. Results: Of the 26 patients with chronic diarrhea, MC was found in 5 (3 lymphocytic colitis and 2 collagenous colitis). Significantly higher polymorphonuclear infiltration was seen in group A as compared with group B (13.8 [5.4–20.6] vs 7.2 [0–19.6]; P = 0.03) or group C (13.8 [5.4–20.6] vs 4 [0–13.4]; P = 0.007). Intraepithelial lymphocytes (12 [4–32] vs 4 [0–24]; P = 0.008) and basement membrane thickening (3.5 [2.9–10.6] vs 2.5 [1.6–5.86]; P = 0.008) were also significantly higher in group A as compared with group C. Conclusions: MC was found to be present in children with nonbloody chronic diarrhea in children. Further multicentric studies may provide adequate data on its prevalence.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1097/MPG.0b013e3182942868</identifier><identifier>PMID: 23549325</identifier><identifier>CODEN: JPGND6</identifier><language>eng</language><publisher>Hagerstown, MD: by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</publisher><subject>Biological and medical sciences ; Biopsy ; Child ; Child, Preschool ; Chronic Disease ; Colitis, Collagenous - complications ; Colitis, Collagenous - epidemiology ; Colitis, Collagenous - pathology ; Colitis, Lymphocytic - complications ; Colitis, Lymphocytic - epidemiology ; Colitis, Lymphocytic - pathology ; collagenous colitis ; Colonoscopy ; Diarrhea - etiology ; Diarrhea - pathology ; diarrhea in children ; Feeding. Feeding behavior ; Female ; Fundamental and applied biological sciences. Psychology ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Intestinal Mucosa - pathology ; Lymphocytes - pathology ; lymphocytic colitis ; Male ; Medical sciences ; microscopic colitis ; Neutrophil Infiltration ; Neutrophils ; Other diseases. Semiology ; Stomach. Duodenum. Small intestine. Colon. Rectum. 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Methods: A total of 100 consecutive children ages 3 to 12 years, with nonbloody diarrhea (passage of ≥3 loose stools per day) of &gt;12 weeks' duration were screened and 26 were enrolled in the study in which no specific etiology could be found and colonoscopy did not reveal any mucosal abnormality. Colonic biopsies were evaluated for the presence of lymphocytic colitis or collagenous colitis and those with the characteristic changes were defined to have MC (group A). Colonic biopsies from patients with MC were compared with biopsies from patients with chronic diarrhea but no evidence of MC (group B). One hundred children ages 3 to 12 years with bleeding per rectum were screened and colonic biopsies from 45 patients (group C) who had colonic mucosal changes but no vascular or polyp lesion were compared with patients with MC. Results: Of the 26 patients with chronic diarrhea, MC was found in 5 (3 lymphocytic colitis and 2 collagenous colitis). Significantly higher polymorphonuclear infiltration was seen in group A as compared with group B (13.8 [5.4–20.6] vs 7.2 [0–19.6]; P = 0.03) or group C (13.8 [5.4–20.6] vs 4 [0–13.4]; P = 0.007). Intraepithelial lymphocytes (12 [4–32] vs 4 [0–24]; P = 0.008) and basement membrane thickening (3.5 [2.9–10.6] vs 2.5 [1.6–5.86]; P = 0.008) were also significantly higher in group A as compared with group C. Conclusions: MC was found to be present in children with nonbloody chronic diarrhea in children. 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Abdomen</subject><subject>Humans</subject><subject>Intestinal Mucosa - pathology</subject><subject>Lymphocytes - pathology</subject><subject>lymphocytic colitis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>microscopic colitis</subject><subject>Neutrophil Infiltration</subject><subject>Neutrophils</subject><subject>Other diseases. Semiology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM1OGzEURq0KVALtG6AqG6RuBnz9N55FFzQtFASUBahLy-O5Vtw6M8GeCOXtcUQoEisWlnWl8_m7PoQcAj0G2tQn17fnx7SlwJGDZo1gWukPZAKSq0poCjtkQlldVwxA7ZH9nP9SSmsh6Ueyx7gUDWdyQuR1cGnIblgGN50NMYwhT0M_nc1D7BL20z9hnJcpDX0BfgSb0hztJ7Lrbcz4eXsfkPuzn3ezX9XV7_OL2elV5YRmUDWeeoeIbQPStq1Hhta1AlErAb4glnuruagdSN_xzjkJrqzI0HeqAcUPyNfnd5dpeFhhHs0iZIcx2h6HVTYggINiJVFQ8YxuvpMTerNMYWHT2gA1G2GmCDNvhZXYl23Dql1g9z_0YqgAR1vAZmejT7Z3Ib9ytaxBNvDa_zjEEVP-F1ePmEyRFce5KeqphFpVrPRTXaaqHLaJfdvGQsT1u3Y2l7c3_PsZVVJz_gQLYJTZ</recordid><startdate>201308</startdate><enddate>201308</enddate><creator>Singh, Prashant</creator><creator>Das, Prasenjit</creator><creator>Jain, A.K.</creator><creator>Mathan, Minnie</creator><creator>Mathur, Meera</creator><creator>Bhat, Abdus Sami</creator><creator>Varma, Sharat</creator><creator>Chaturvedi, Mona K.</creator><creator>Gupta, Siddhartha Datta</creator><creator>Bhatnagar, Shinjini</creator><general>by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</general><general>Lippincott Williams &amp; Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201308</creationdate><title>Microscopic Colitis in Children With Chronic Diarrhea</title><author>Singh, Prashant ; Das, Prasenjit ; Jain, A.K. ; Mathan, Minnie ; Mathur, Meera ; Bhat, Abdus Sami ; Varma, Sharat ; Chaturvedi, Mona K. ; Gupta, Siddhartha Datta ; Bhatnagar, Shinjini</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4821-9f0fceeeb915abbfe2eacb4ee8641f482a3fa8347c15fd3dcc51c7452efd69163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chronic Disease</topic><topic>Colitis, Collagenous - complications</topic><topic>Colitis, Collagenous - epidemiology</topic><topic>Colitis, Collagenous - pathology</topic><topic>Colitis, Lymphocytic - complications</topic><topic>Colitis, Lymphocytic - epidemiology</topic><topic>Colitis, Lymphocytic - pathology</topic><topic>collagenous colitis</topic><topic>Colonoscopy</topic><topic>Diarrhea - etiology</topic><topic>Diarrhea - pathology</topic><topic>diarrhea in children</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Intestinal Mucosa - pathology</topic><topic>Lymphocytes - pathology</topic><topic>lymphocytic colitis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>microscopic colitis</topic><topic>Neutrophil Infiltration</topic><topic>Neutrophils</topic><topic>Other diseases. Semiology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Prashant</creatorcontrib><creatorcontrib>Das, Prasenjit</creatorcontrib><creatorcontrib>Jain, A.K.</creatorcontrib><creatorcontrib>Mathan, Minnie</creatorcontrib><creatorcontrib>Mathur, Meera</creatorcontrib><creatorcontrib>Bhat, Abdus Sami</creatorcontrib><creatorcontrib>Varma, Sharat</creatorcontrib><creatorcontrib>Chaturvedi, Mona K.</creatorcontrib><creatorcontrib>Gupta, Siddhartha Datta</creatorcontrib><creatorcontrib>Bhatnagar, Shinjini</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singh, Prashant</au><au>Das, Prasenjit</au><au>Jain, A.K.</au><au>Mathan, Minnie</au><au>Mathur, Meera</au><au>Bhat, Abdus Sami</au><au>Varma, Sharat</au><au>Chaturvedi, Mona K.</au><au>Gupta, Siddhartha Datta</au><au>Bhatnagar, Shinjini</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microscopic Colitis in Children With Chronic Diarrhea</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2013-08</date><risdate>2013</risdate><volume>57</volume><issue>2</issue><spage>240</spage><epage>244</epage><pages>240-244</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><coden>JPGND6</coden><abstract>ABSTRACT Objective: The aim of the present study was to study microscopic colitis (MC) in children with special reference to its role in chronic diarrhea and changes in mucosal biopsies. Methods: A total of 100 consecutive children ages 3 to 12 years, with nonbloody diarrhea (passage of ≥3 loose stools per day) of &gt;12 weeks' duration were screened and 26 were enrolled in the study in which no specific etiology could be found and colonoscopy did not reveal any mucosal abnormality. Colonic biopsies were evaluated for the presence of lymphocytic colitis or collagenous colitis and those with the characteristic changes were defined to have MC (group A). Colonic biopsies from patients with MC were compared with biopsies from patients with chronic diarrhea but no evidence of MC (group B). One hundred children ages 3 to 12 years with bleeding per rectum were screened and colonic biopsies from 45 patients (group C) who had colonic mucosal changes but no vascular or polyp lesion were compared with patients with MC. Results: Of the 26 patients with chronic diarrhea, MC was found in 5 (3 lymphocytic colitis and 2 collagenous colitis). Significantly higher polymorphonuclear infiltration was seen in group A as compared with group B (13.8 [5.4–20.6] vs 7.2 [0–19.6]; P = 0.03) or group C (13.8 [5.4–20.6] vs 4 [0–13.4]; P = 0.007). Intraepithelial lymphocytes (12 [4–32] vs 4 [0–24]; P = 0.008) and basement membrane thickening (3.5 [2.9–10.6] vs 2.5 [1.6–5.86]; P = 0.008) were also significantly higher in group A as compared with group C. Conclusions: MC was found to be present in children with nonbloody chronic diarrhea in children. Further multicentric studies may provide adequate data on its prevalence.</abstract><cop>Hagerstown, MD</cop><pub>by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology</pub><pmid>23549325</pmid><doi>10.1097/MPG.0b013e3182942868</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Journals@Ovid Complete; Wiley Online Library All Journals
subjects Biological and medical sciences
Biopsy
Child
Child, Preschool
Chronic Disease
Colitis, Collagenous - complications
Colitis, Collagenous - epidemiology
Colitis, Collagenous - pathology
Colitis, Lymphocytic - complications
Colitis, Lymphocytic - epidemiology
Colitis, Lymphocytic - pathology
collagenous colitis
Colonoscopy
Diarrhea - etiology
Diarrhea - pathology
diarrhea in children
Feeding. Feeding behavior
Female
Fundamental and applied biological sciences. Psychology
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Intestinal Mucosa - pathology
Lymphocytes - pathology
lymphocytic colitis
Male
Medical sciences
microscopic colitis
Neutrophil Infiltration
Neutrophils
Other diseases. Semiology
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Vertebrates: anatomy and physiology, studies on body, several organs or systems
title Microscopic Colitis in Children With Chronic Diarrhea
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