Granulomatous appendicitis in children: A single institutional experience

Background: Granulomatous appendicitis (GA) is a rare entity, mostly mentioned in adults. There have been anecdotal case reports describing GA in the paediatric population. This study was aimed at reviewing the cases of appendectomies to assess the incidence and characteristics of GA in children in...

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Main Author: Kamalesh Pal
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:African Journal of Paediatric Surgery
Subjects:
Online Access:http://www.afrjpaedsurg.org/article.asp?issn=0189-6725;year=2014;volume=11;issue=1;spage=26;epage=31;aulast=Pal
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spelling doaj-1cefc617d7604d2aa4fc71d3518009672020-11-24T22:50:26ZengWolters Kluwer Medknow PublicationsAfrican Journal of Paediatric Surgery0189-67250974-59982014-01-01111263110.4103/0189-6725.129207Granulomatous appendicitis in children: A single institutional experienceKamalesh PalBackground: Granulomatous appendicitis (GA) is a rare entity, mostly mentioned in adults. There have been anecdotal case reports describing GA in the paediatric population. This study was aimed at reviewing the cases of appendectomies to assess the incidence and characteristics of GA in children in a tertiary care University hospital. Materials and Methods: Records of children (<13 years age) with biopsy proven granulomatous lesions in the appendectomy specimen, treated during 1991-2011, were analysed. Data regarding demography, clinical presentation, radiological findings, intra-operative finding, histology, diagnosis and follow-up were recorded and descriptively analysed. Results: Twelve out of 1150 (1.04%) appendectomies were biopsy proven GA. Male to female ratio was 8:4. Four had Yersinia enterocolitis, two had Crohn′s disease (CD; one isolated Crohn′s Appendicitis, one Ileo-cecal Crohn′ with appendicitis) and five were idiopathic. Remaining one case, initially diagnosed as idiopathic GA, developed full blown ileo-cecal CD at 2 nd month post-operative. Age ranged between 4 and 11 years with inflammatory bowel disease (IBD) affecting older children and Yersinia, seen in younger children. Majority (10/12) remained asymptomatic at a maximum of 5 years of follow-up. Two patients had recurrent symptoms; one with sub-acute obstruction (2 years follow-up) and another with flaring of Crohn′s ileitis (2 months follow-up). Conclusions: GA in children is a rare entity, with incidence of 1.04% and male preponderance in our series. Idiopathic causes were the most common followed by Yersinia enterocolitis and CD. Although majority remained asymptomatic, IBD should be ruled out in case of recurrence of pain or alteration of bowel habit. Therefore, a long-term follow-up (at least for 5 years) of idiopathic GA is suggested in children.http://www.afrjpaedsurg.org/article.asp?issn=0189-6725;year=2014;volume=11;issue=1;spage=26;epage=31;aulast=PalchildrenCrohn′sgranulomatous appendicitisidiopathicYersinia
collection DOAJ
language English
format Article
sources DOAJ
author Kamalesh Pal
spellingShingle Kamalesh Pal
Granulomatous appendicitis in children: A single institutional experience
African Journal of Paediatric Surgery
children
Crohn′s
granulomatous appendicitis
idiopathic
Yersinia
author_facet Kamalesh Pal
author_sort Kamalesh Pal
title Granulomatous appendicitis in children: A single institutional experience
title_short Granulomatous appendicitis in children: A single institutional experience
title_full Granulomatous appendicitis in children: A single institutional experience
title_fullStr Granulomatous appendicitis in children: A single institutional experience
title_full_unstemmed Granulomatous appendicitis in children: A single institutional experience
title_sort granulomatous appendicitis in children: a single institutional experience
publisher Wolters Kluwer Medknow Publications
series African Journal of Paediatric Surgery
issn 0189-6725
0974-5998
publishDate 2014-01-01
description Background: Granulomatous appendicitis (GA) is a rare entity, mostly mentioned in adults. There have been anecdotal case reports describing GA in the paediatric population. This study was aimed at reviewing the cases of appendectomies to assess the incidence and characteristics of GA in children in a tertiary care University hospital. Materials and Methods: Records of children (<13 years age) with biopsy proven granulomatous lesions in the appendectomy specimen, treated during 1991-2011, were analysed. Data regarding demography, clinical presentation, radiological findings, intra-operative finding, histology, diagnosis and follow-up were recorded and descriptively analysed. Results: Twelve out of 1150 (1.04%) appendectomies were biopsy proven GA. Male to female ratio was 8:4. Four had Yersinia enterocolitis, two had Crohn′s disease (CD; one isolated Crohn′s Appendicitis, one Ileo-cecal Crohn′ with appendicitis) and five were idiopathic. Remaining one case, initially diagnosed as idiopathic GA, developed full blown ileo-cecal CD at 2 nd month post-operative. Age ranged between 4 and 11 years with inflammatory bowel disease (IBD) affecting older children and Yersinia, seen in younger children. Majority (10/12) remained asymptomatic at a maximum of 5 years of follow-up. Two patients had recurrent symptoms; one with sub-acute obstruction (2 years follow-up) and another with flaring of Crohn′s ileitis (2 months follow-up). Conclusions: GA in children is a rare entity, with incidence of 1.04% and male preponderance in our series. Idiopathic causes were the most common followed by Yersinia enterocolitis and CD. Although majority remained asymptomatic, IBD should be ruled out in case of recurrence of pain or alteration of bowel habit. Therefore, a long-term follow-up (at least for 5 years) of idiopathic GA is suggested in children.
topic children
Crohn′s
granulomatous appendicitis
idiopathic
Yersinia
url http://www.afrjpaedsurg.org/article.asp?issn=0189-6725;year=2014;volume=11;issue=1;spage=26;epage=31;aulast=Pal
work_keys_str_mv AT kamaleshpal granulomatousappendicitisinchildrenasingleinstitutionalexperience
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