期刊论文详细信息
BMC Gastroenterology
Paneth cell metaplasia in newly diagnosed inflammatory bowel disease in children
Alan WH Bates2  Alan Phillips2  Evi Karanika2  Mark Furman2  Naomi Simmonds1 
[1] Tissue Sciences, St Thomas’s Hospital, London SE1 7EH, UK;Child Health Department, Royal Free Hospital, London NW3 2QG, UK
关键词: Crohn’s disease;    Ulcerative colitis;    Paediatric;    Metaplasia;    Paneth cell;   
Others  :  855229
DOI  :  10.1186/1471-230X-14-93
 received in 2013-11-21, accepted in 2014-05-09,  发布年份 2014
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【 摘 要 】

Background

Paneth cell metaplasia (PCM) is well described in adults but little is known about the distribution of colonic Paneth cells and the occurrence of PCM in a paediatric population. The aim of this study is to determine whether Paneth cell hyperplasia or metaplasia characteristically occurs in the colons of children with newly diagnosed idiopathic inflammatory bowel disease (IBD).

Methods

We retrospectively reviewed colonic series from 28 new diagnoses of paediatric IBD at a tertiary referral centre, and from a further 14 children with IBD-like symptoms whose colonic biopsies and ancillary investigations were normal. Paneth cells were counted at 6 anatomical sites in the colon, and at each site acute and chronic inflammation were assessed semi-quantitatively and the presence or absence of crypt architectural distortion and eosinophilia was documented.

Results

In control, ulcerative colitis (UC) and Crohn’s disease (CD) groups there was a gradient of decreasing Paneth cell numbers from caecum to rectum. Paneth cells were not seen in the distal colon in the control group, but they were present there in 11 of 13 patients with ulcerative colitis and 14 of 15 with Crohn’s disease. Only patients with IBD showed Paneth cell hyperplasia, assessed as more than 10 Paneth cells per 10 well-oriented crypts at any site. There was a statistically significant increase in Paneth cells in the caecum, ascending, transverse and descending colon in UC and in the ascending, transverse, descending and sigmoid colon in CD compared with controls. There was no significant difference between UC and CD. There was no correlation between the site of PCM and acute or chronic inflammation, crypt distortion or eosinophilia.

Conclusion

Paneth cells are found in the proximal but not the distal colon in otherwise normal paediatric colonic series. A high proportion of UC and CD patients show PCM in the distal colon. This is present early in the disease and does not correlate with histological features of chronicity.

【 授权许可】

   
2014 Simmonds et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Paneth J: Ueber die secernirenden Zellen des Dünndarm-Epithels. Arch Mikroskop Anat 1888, 31:113-191.
  • [2]Paterson JC, Watson SH: Paneth cell metaplasia in ulcerative colitis. Am J Pathol 1961, 38:243-249.
  • [3]Erlandsen SL, Parsons JA, Taylor TD: Ultrastructural immunocytochemical localization of lysozyme in the Paneth cells of man. J Histochem Cytochem 1974, 22:401-413.
  • [4]Kiyohara H, Egami H, Shibata Y, Murata K, Ohshima S, Ogawa M: Light microscopic immunohistochemical analysis of the distribution of group II phospholipase A2 in human digestive organs. J Histochem Cytochem 1992, 40:1659-1664.
  • [5]Jones DE, Bevins CL: Defensin-6 mRNA in human Paneth cells: implications for antimicrobial peptides in host defense of the human bowel. FEBS Lett 1993, 315:187-192.
  • [6]Bevins CL, Salzman NH: Paneth cells, antimicrobial peptides and maintenance of intestinal homeostasis. Nat Rev Microbiol 2011, 9:356-368.
  • [7]Gersemann M, Wehkamp J, Stange EF: Innate immune dysfunction in inflammatory bowel disease. J Intern Med 2012, 271:421-428.
  • [8]Salzman NH, Underwood MA, Bevins CL: Paneth cells, defensins, and the commensal microbiota: a hypothesis on intimate interplay at the intestinal mucosa. Semin Immunol 2007, 19:70-83.
  • [9]Mathan M, Hughes J, Whitehead R: The morphogenesis of the human Paneth cell: an immunocytochemical ultrastructural study. Histochemistry 1987, 87:91-96.
  • [10]Thomson AB, Chopra A, Clandinin MT, Freeman H: Recent advances in small bowel diseases: Part I. World J Gastroenterol 2012, 18:3336-3352.
  • [11]Tanaka M, Saito H, Kusumi T, Fukuda S, Shimoyama T, Sasaki Y, Suto K, Munakata A, Kudo H: Spatial distribution and histogenesis of colorectal Paneth cell metaplasia in idiopathic inflammatory bowel disease. J Gastroenterol Hepatol 2001, 16:1353-1359.
  • [12]Symonds DA: Paneth cell metaplasia in diseases of the colon and rectum. Arch Pathol 1974, 97:343-347.
  • [13]Mitsuhashi J, Mikami T, Saigenji K, Okayasu I: Significant correlation of morphological remodeling in ulcerative colitis with disease duration and between elevated p53 and p21 expression in rectal mucosa and neoplastic development. Pathol Int 2005, 55:113-121.
  • [14]Jenkins D, Balsitis M, Gallivan S, Dixon MF, Gilmour HM, Shepherd NA, Theodossi A, Williams GT: Guidelines for the initial biopsy diagnosis of suspected chronic idiopathic inflammatory bowel disease: the British Society of Gastroenterology Initiative. J Clin Pathol 1997, 50:93-105.
  • [15]Puiman PJ, Burger-Van Paassen N, Schaart MW, De Bruijn AC, De Krijger RR, Tibboel D, Van Goudoever JB, Renes IB: Paneth cell hyperplasia and metaplasia in necrotizing enterocolitis. Pediatr Res 2011, 69:217-223.
  • [16]Schumacher G: First attack of inflammatory bowel disease and infectious colitis. A clinical, histological and microbiological study with special reference to early diagnosis. Scand J Gastroenterol Suppl 1993, 198:1-24.
  • [17]Dundas SA, Dutton J, Skipworth P: Reliability of rectal biopsy in distinguishing between chronic inflammatory bowel disease and acute self-limiting colitis. Histopathology 1997, 31:60-66.
  • [18]Glickman JN, Bousvaros A, Farraye FA, Zholudev A, Friedman S, Wang HH, Leichtner AM, Odze RD: Pediatric patients with untreated ulcerative colitis may present initially with unusual morphologic findings. Am J Surg Pathol 2004, 28:190-197.
  • [19]Kelly P, Feakins R, Domizio P, Murphy J, Bevins C, Wilson J, McPhail G, Poulsom R, Dhaliwal W: Paneth cell granule depletion in the human small intestine under infective and nutritional stress. Clin Exp Immunol 2004, 135:303-309.
  • [20]Behjati S, Zilbauer M, Heuschkel R, Phillips A, Salvestrini C, Torrente F, Bates AW: Defining eosinophilic colitis in children: insights from a retrospective case series. J Pediatr Gastroenterol Nutr 2009, 49:208-15.
  • [21]Adolph TE, Tomczak MF, Niederreiter L, Ko HJ, Böck J, Martinez-Naves E, Glickman JN, Tschurtschenthaler M, Hartwig J, Hosomi S, Flak MB, Cusick JL, Kohno K, Iwawaki T, Billmann-Born S, Raine T, Bharti R, Lucius R, Kweon MN, Marciniak SJ, Choi A, Hagen SJ, Schreiber S, Rosenstiel P, Kaser A, Blumberg RS: Paneth cells as a site of origin for intestinal inflammation. Nature 2013, 503:272-6.
  • [22]Perminow G, Beisner J, Koslowski M, Lyckander LG, Stange E, Vatn MH, Wehkamp J: Defective paneth cell-mediated host defense in pediatric ileal Crohn's disease. Am J Gastroenterol 2010, 105:452-459.
  • [23]Zilbauer M, Jenke A, Wenzel G, Goedde D, Postberg J, Phillips AD, Lucas M, Noble-Jamieson G, Torrente F, Salvestrini C, Heuschkel R, Wirth S: Intestinal alpha-defensin expression in pediatric inflammatory bowel disease. Inflamm Bowel Dis 2011, 17:2076-86.
  • [24]Kumarasinghe MP, Quek TP, Chau CY, Mustapha NR, Luman W, Ooi CJ: Endoscopic biopsy features and diagnostic challenges of adult Crohn’s disease at initial presentation. Pathology 2010, 42:131-137.
  • [25]West AB: The pathology of diverticulitis. J Clin Gastroenterol 2008, 42:1137-1138.
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