{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,11]],"date-time":"2025-10-11T13:22:01Z","timestamp":1760188921035},"reference-count":18,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2007,11,14]],"date-time":"2007-11-14T00:00:00Z","timestamp":1194998400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neurogastroenterology Motil"],"published-print":{"date-parts":[[2008,4]]},"abstract":"<jats:p><jats:bold>Abstract\u2002<\/jats:bold> Chronic intestinal pseudo\u2010obstruction (CIP) is an uncommon disorder that may be of primary or secondary origin. We report a case of a 37\u2010year\u2010old woman with CIP due to inflammatory disorder of unknown origin involving the skin (eosinophilic fasciitis), the lungs (decreased diffusion capacity) and the gastrointestinal tract. History, clinical examination, plain abdominal film, barium X\u2010ray and colonoscopy established a diagnosis of recurrent pseudo\u2010obstruction. A full\u2010thickness biopsy was performed during explorative laparotomy, and histological examination revealed findings compatible with an inflammatory myopathy due to a dense lymphoid infiltrate and extensive loss of the muscularis propriae layers. Immunosuppressive therapy with cyclosporin was initiated, with significant clinical improvement. This case illustrates another form of CIP, characterized by an inflammatory myopathy, which is histologically distinct from other known visceral myopathies and neuropathies.<\/jats:p>","DOI":"10.1111\/j.1365-2982.2007.01033.x","type":"journal-article","created":{"date-parts":[[2007,11,17]],"date-time":"2007-11-17T07:18:49Z","timestamp":1195283929000},"page":"343-348","source":"Crossref","is-referenced-by-count":15,"title":["Chronic intestinal pseudo\u2010obstruction caused by an intestinal inflammatory myopathy: case report and review of the literature"],"prefix":"10.1111","volume":"20","author":[{"given":"S.","family":"Dewit","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G.","family":"De Hertogh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"K.","family":"Geboes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Tack","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2007,11,22]]},"reference":[{"key":"e_1_2_4_2_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2982.2007.00902.x"},{"key":"e_1_2_4_3_2","doi-asserted-by":"publisher","DOI":"10.1053\/j.gastro.2005.06.081"},{"key":"e_1_2_4_4_2","doi-asserted-by":"publisher","DOI":"10.1016\/0016-5085(85)90587-6"},{"key":"e_1_2_4_5_2","first-page":"823","article-title":"Idiopathic myositis of the small intestine. 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