Literature DB >> 7128379

Amyloid colitis.

S E Vernon.   

Abstract

Amyloidosis not infrequently involves the gastrointestinal tract and may result in a variety of symptoms, including those related to impaired motility, malabsorption, and ulceration due to ischemia. This report describes the case of a 74-year-old man with systemic amyloidosis secondary to multiple myeloma, with striking gross morphologic findings involving the colon, seen at autopsy, resembling severe inflammatory bowel disease. Microscopically, the small arterioles of the lamina propria were markedly narrowed or occluded by massive deposition of amyloid, presumably leading to diffuse ischemia and mucosal necrosis. Although the radiologic appearance of this condition has been well recognized, and ischemia due to amyloidosis has been described, this case is presented to demonstrate the gross anatomic changes not illustrated in previous reviews of the subject.

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Year:  1982        PMID: 7128379     DOI: 10.1007/bf02629550

Source DB:  PubMed          Journal:  Dis Colon Rectum        ISSN: 0012-3706            Impact factor:   4.585


  3 in total

1.  Primary systemic amyloidosis presenting as idiopathic inflammatory colitis.

Authors:  Nadeem Rahman; Muhammad Toqeer; Ian Hawley; Simon Weston-Smith; Mark W Whitehead; Johan Willem Rademaker; Eric McWilliams
Journal:  BMJ Case Rep       Date:  2011-10-04

Review 2.  Secondary intestinal amyloidosis presenting intractable hematochezia: a case report and literature review.

Authors:  So Hyun Kim; Jae Hwang Kim; Mi Jin Gu
Journal:  Int J Clin Exp Pathol       Date:  2014-03-15

3.  Small intestinal amyloidosis: a rare cause of diverticular disease.

Authors:  Gabriel M Groisman; Hector I Cohen
Journal:  Case Rep Pathol       Date:  2014-06-05
  3 in total

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