Literature DB >> 26906301

Terminal Ileitis as a Feature of Henoch-Schönlein Purpura Masquerading as Crohn Disease in Adults.

Hemal N Sampat1, Brian P McAllister, Darryl D Gaines, Barbara Ostrov.   

Abstract

Henoch-Schönlein purpura (HSP), more recently termed immunoglobulin A (IgA) vasculitis, is a systemic small-vessel vasculitis characterized by perivascular IgA deposition. This disease manifests clinically as palpable purpura, arthralgia, gastrointestinal symptoms, and renal dysfunction. Although ileitis can be seen in HSP, terminal ileitis is virtually pathognomonic for Crohn disease. We present a comprehensive review of the literature on this association, including 2 cases of our own, to demonstrate the importance of considering HSP in the differential diagnosis of ileitis suggestive of Crohn disease. We review the growing body of literature suggesting a pathophysiologic link between the conditions, possibly through an IgA-mediated mechanism.

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Year:  2016        PMID: 26906301     DOI: 10.1097/RHU.0000000000000361

Source DB:  PubMed          Journal:  J Clin Rheumatol        ISSN: 1076-1608            Impact factor:   3.517


  3 in total

1.  Avoiding "Rash" Conclusions: Challenge of IgA Vasculitis in Adults.

Authors:  S Hu; A Birg; M Hovaida; M W Gavin; D McCarthy
Journal:  Dig Dis Sci       Date:  2017-04       Impact factor: 3.199

2.  Terminal Ileitis as the Presenting Feature of Henoch-Schönlein Purpura in a 22-Year-Old Male.

Authors:  Muhammad Waleed; Swaminathan Perinkulam Sathyanarayanan; Soban Arif Maan; Linta Mansoor; Kayla Hoerschgen
Journal:  Cureus       Date:  2021-11-09

3.  Adult-Onset Immunoglobulin A Vasculitis.

Authors:  Matthew Chadwick; Leonid Shamban; John Macksood
Journal:  ACG Case Rep J       Date:  2020-03-16
  3 in total

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