The pathogenesis of idiopathic megacolon
Even today, the pathogenesis of idiopathic megacolon is still a subject of controversy. Anomalies of the gastrointestinal autonomous nervous system or of the smooth muscle of the muscularis propria are being considered. Sixty-three idiopathic megacolon resections between 1997 and June 2004 were inve...
Saved in:
Published in | European journal of gastroenterology & hepatology Vol. 18; no. 11; p. 1209 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
01.11.2006
|
Subjects | |
Online Access | Get more information |
ISSN | 0954-691X |
DOI | 10.1097/01.meg.0000236883.13720.c2 |
Cover
Loading…
Abstract | Even today, the pathogenesis of idiopathic megacolon is still a subject of controversy. Anomalies of the gastrointestinal autonomous nervous system or of the smooth muscle of the muscularis propria are being considered.
Sixty-three idiopathic megacolon resections between 1997 and June 2004 were investigated. The native specimens were coiled caudo-cranially and cryostat-cut. Connective tissue was stained with picric acid/Sirius red after Delauney fixation. Immunohistochemistry was performed for collagen types I, II, III and IV, as well as smooth muscle actin, vimentin, desmin fibronectin and CD117 for interstitial cells of Cajal. The enteric nervous system was examined by enzyme histochemistry for acetylcholine-esterase, lactate dehydrogenase, succinic dehydrogenase and nitroxide synthase.
Histologically, idiopathic megacolon was characterized by a total atrophy of the collagenous tendinous connective tissue membrane of the myenteric plexus and the tendinous collagen fibre net of the muscularis propria. Immunohistochemically, mainly collagen type III was missing in the muscularis propria. Interestingly, the incidence of idiopathic megacolon in those of the female sex was seven times more frequent than in the male sex. The myenteric plexus was normal in the majority of patients. Interstitial cells of Cajal, collagen II and IV, as well as smooth muscle actin, desmin and fibronectin showed no consistent alteration.
A normally structured tendinous fibre net of muscularis propria is an essential prerequisite for effective gut peristalsis. Atrophy of the tendinous fibre net abolishes peristalsis and allows for unlimited distension of the colon. A diagnosis of idiopathic megacolon can reliably be made on a collagen stain. The normal findings of myenteric plexus support the hypothesis that a primary metabolic defect of muscularis propria may be the underlying cause of idiopathic megacolon. |
---|---|
AbstractList | Even today, the pathogenesis of idiopathic megacolon is still a subject of controversy. Anomalies of the gastrointestinal autonomous nervous system or of the smooth muscle of the muscularis propria are being considered.
Sixty-three idiopathic megacolon resections between 1997 and June 2004 were investigated. The native specimens were coiled caudo-cranially and cryostat-cut. Connective tissue was stained with picric acid/Sirius red after Delauney fixation. Immunohistochemistry was performed for collagen types I, II, III and IV, as well as smooth muscle actin, vimentin, desmin fibronectin and CD117 for interstitial cells of Cajal. The enteric nervous system was examined by enzyme histochemistry for acetylcholine-esterase, lactate dehydrogenase, succinic dehydrogenase and nitroxide synthase.
Histologically, idiopathic megacolon was characterized by a total atrophy of the collagenous tendinous connective tissue membrane of the myenteric plexus and the tendinous collagen fibre net of the muscularis propria. Immunohistochemically, mainly collagen type III was missing in the muscularis propria. Interestingly, the incidence of idiopathic megacolon in those of the female sex was seven times more frequent than in the male sex. The myenteric plexus was normal in the majority of patients. Interstitial cells of Cajal, collagen II and IV, as well as smooth muscle actin, desmin and fibronectin showed no consistent alteration.
A normally structured tendinous fibre net of muscularis propria is an essential prerequisite for effective gut peristalsis. Atrophy of the tendinous fibre net abolishes peristalsis and allows for unlimited distension of the colon. A diagnosis of idiopathic megacolon can reliably be made on a collagen stain. The normal findings of myenteric plexus support the hypothesis that a primary metabolic defect of muscularis propria may be the underlying cause of idiopathic megacolon. |
Author | Müller-Lobeck, Heinrich Bruder, Elisabeth Meier-Ruge, William A Stoss, Franz |
Author_xml | – sequence: 1 givenname: William A surname: Meier-Ruge fullname: Meier-Ruge, William A email: dsc.oberwill@bluewin.ch organization: Department of Pathology, University Medical School, Basel, Switzerland. dsc.oberwill@bluewin.ch – sequence: 2 givenname: Heinrich surname: Müller-Lobeck fullname: Müller-Lobeck, Heinrich – sequence: 3 givenname: Franz surname: Stoss fullname: Stoss, Franz – sequence: 4 givenname: Elisabeth surname: Bruder fullname: Bruder, Elisabeth |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17033443$$D View this record in MEDLINE/PubMed |
BookMark | eNo1jjtPwzAURj0U0Qf8BRQxsSTc6-vE8YgqXlIlliKxVX5ct0FNHNUw9N-3CPiWI53h6JuLyZAGFuIWoUIw-h6w6nlbwXmSmralCklLqLyciBmYWpWNwY-pmOf8CYCaUF-KKWogUopm4m6942K0X7u05YFzl4sUiy506cd1vjjHrU_7NFyJi2j3ma__uBDvT4_r5Uu5ent-XT6sSk9G1mWsWWNURhK72EoVgoHWsMe6aRw5CcFpHax3yoKj6NAZr6UhttY3GGu5EDe_3fHb9Rw246Hr7eG4-b8sTxY4RW4 |
CitedBy_id | crossref_primary_10_1111_j_1440_1746_2009_05940_x crossref_primary_10_1590_0037_8682_0505_2016 crossref_primary_10_1055_a_2360_5008 crossref_primary_10_1111_ans_15868 crossref_primary_10_1007_s00418_020_01947_w crossref_primary_10_1007_s00261_009_9517_8 crossref_primary_10_1016_j_gie_2007_08_031 crossref_primary_10_1007_s00292_007_0896_8 crossref_primary_10_1007_s00535_008_2207_4 crossref_primary_10_1186_s12876_018_0753_7 crossref_primary_10_1016_j_ijscr_2022_106777 crossref_primary_10_1111_j_1463_1318_2007_01457_x crossref_primary_10_1016_j_fmc_2016_07_010 crossref_primary_10_1053_j_sempedsurg_2009_07_002 crossref_primary_10_1007_s11938_007_0017_z crossref_primary_10_7759_cureus_75229 crossref_primary_10_1007_s00384_017_2894_5 crossref_primary_10_1136_bcr_2020_240209 crossref_primary_10_1097_MEG_0b013e3280116cb8 crossref_primary_10_1136_jclinpath_2021_207413 crossref_primary_10_2298_AVB1003273P crossref_primary_10_2298_AVB0901053P crossref_primary_10_1007_s10620_015_3645_5 |
ContentType | Journal Article |
DBID | CGR CUY CVF ECM EIF NPM |
DOI | 10.1097/01.meg.0000236883.13720.c2 |
DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed |
DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) |
DatabaseTitleList | MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | no_fulltext_linktorsrc |
Discipline | Medicine |
ExternalDocumentID | 17033443 |
Genre | Journal Article |
GroupedDBID | --- .-D .Z2 0R~ 4Q1 4Q2 4Q3 53G 5GY 5VS 6PF 71W 8L- AAAAV AAHPQ AAIQE AAMTA AARTV AASCR AAUEB AAWTL AAYEP ABASU ABBUW ABDIG ABJNI ABOCM ABVCZ ABXVJ ABZAD ACCJW ACDDN ACEWG ACGFO ACGFS ACILI ACWDW ACWRI ACXJB ACXNZ ADFPA ADGGA ADHPY ADNKB AE3 AE6 AEETU AENEX AFDTB AFSOK AFUWQ AGINI AHQNM AHVBC AINUH AJCLO AJIOK AJNWD AJNYG AJZMW AKCTQ ALKUP ALMA_UNASSIGNED_HOLDINGS ALMTX AMJPA AMKUR AMNEI AOHHW AWKKM BQLVK BS7 C45 CAG CGR COF CS3 CUY CVF DIWNM DUNZO E.X EBS ECM EEVPB EIF EJD EX3 F5P FCALG FL- GNXGY GQDEL H0~ HLJTE HZ~ IKREB IN~ IPNFZ JF9 JG8 JK3 JK8 K8S KD2 L-C N9A NPM N~M O9- OAG OAH OCUKA ODA OJAPA OLG OLW OPUJH ORVUJ OUVQU OVD OVDNE OVOZU OWU OWV OWW OWX OWY OWZ OXXIT P-K P2P R58 RIG RLZ S4R S4S T8P TEORI TSPGW V2I VVN W3M WOQ WOW X3V X3W XXN XYM YFH ZFV ZZMQN |
ID | FETCH-LOGICAL-c3925-f5e71f4923ebf824dd9089ec1566b3b20db77dacb4a0b3fb1b9c7293eaac61f52 |
ISSN | 0954-691X |
IngestDate | Wed Feb 19 01:44:10 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 11 |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c3925-f5e71f4923ebf824dd9089ec1566b3b20db77dacb4a0b3fb1b9c7293eaac61f52 |
PMID | 17033443 |
ParticipantIDs | pubmed_primary_17033443 |
PublicationCentury | 2000 |
PublicationDate | 2006-November |
PublicationDateYYYYMMDD | 2006-11-01 |
PublicationDate_xml | – month: 11 year: 2006 text: 2006-November |
PublicationDecade | 2000 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | European journal of gastroenterology & hepatology |
PublicationTitleAlternate | Eur J Gastroenterol Hepatol |
PublicationYear | 2006 |
References | 17413291 - Eur J Gastroenterol Hepatol. 2007 May;19(5):399-400 |
References_xml | – reference: 17413291 - Eur J Gastroenterol Hepatol. 2007 May;19(5):399-400 |
SSID | ssj0017317 |
Score | 1.9480766 |
Snippet | Even today, the pathogenesis of idiopathic megacolon is still a subject of controversy. Anomalies of the gastrointestinal autonomous nervous system or of the... |
SourceID | pubmed |
SourceType | Index Database |
StartPage | 1209 |
SubjectTerms | Adolescent Adult Aged Atrophy Case-Control Studies Coiled Bodies - pathology Collagen Type III - analysis Colon - chemistry Colon - innervation Colon - pathology Connective Tissue - chemistry Connective Tissue - pathology Enteric Nervous System - enzymology Enteric Nervous System - pathology Female Histocytochemistry - methods Humans Immunohistochemistry - methods Male Megacolon - metabolism Megacolon - pathology Megacolon - physiopathology Middle Aged Muscle, Smooth - pathology Myenteric Plexus - pathology Sex Factors |
Title | The pathogenesis of idiopathic megacolon |
URI | https://www.ncbi.nlm.nih.gov/pubmed/17033443 |
Volume | 18 |
hasFullText | |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LSwMxEA5VQbyI77fswYMgKZt9Zo8qioj14AO8SZJNalF3RbcX_4H_2plNtq3SinpZyoYuzX7TycyXzDeE7MU8UzzRATXCZBTWW055lic0DZnxldKYhOBpi8vk7DY6v4vvWq2PkVNL_Uq21fvYupL_oAr3AFeskv0DsoOHwg34DPjCFRCG668xxpbCZRc9llUW6eW9sm4zrA6edbcWpS4m0u8uFO2Kt-q1RHXOVyvJhPbwAAtV9YV072hYQ-lV33Zjd0zNkAzt4Kb70THWFtKLElB7tOtarwBfO2CdryvXpx1D5vchG9DPXeXNE6r-2nNmo3wEG_ARDbEY0SSrG-GM8bH9ps7EeUys3R3ryq1EsM_a8LJqlckgTDgP2wz76rRVMPolgOXluQaZgQcLI6v89PPoN5ntZmiKTEHCgR1UkfZx21FguakVbbRTa9RrUf1z4g9EPVr30G85Sx273CyQeZd0eIfWghZJSxdLZLbjjlUsk30wJG_UkLzSeEND8gaGtEJuT09ujs-oa6FBFQS-MTWxTplBET4tDQ-iPMd9Xq0wa5ehDPxcpmkulIyEL0MjmcwUpFuhFkIlzMTBKpkuykKvEy-NdRKHqdA84lGg_UwlPI8Ek37MtQrEBlmzc7x_sTop983sNyeObJG5oQltkxkDf0y9A1FeJXdrBD4B8nRMHw |
linkProvider | National Library of Medicine |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=The+pathogenesis+of+idiopathic+megacolon&rft.jtitle=European+journal+of+gastroenterology+%26+hepatology&rft.au=Meier-Ruge%2C+William+A&rft.au=M%C3%BCller-Lobeck%2C+Heinrich&rft.au=Stoss%2C+Franz&rft.au=Bruder%2C+Elisabeth&rft.date=2006-11-01&rft.issn=0954-691X&rft.volume=18&rft.issue=11&rft.spage=1209&rft_id=info:doi/10.1097%2F01.meg.0000236883.13720.c2&rft_id=info%3Apmid%2F17033443&rft_id=info%3Apmid%2F17033443&rft.externalDocID=17033443 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0954-691X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0954-691X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0954-691X&client=summon |