Literature DB >> 3829862

Enteritis cystica profunda in Peutz-Jeghers syndrome. Report of a case and review of the literature.

A D Dippolito, A Aburano, C A Bezouska, R A Happ.   

Abstract

The hereditary condition known as Peutz-Jeghers syndrome is characterized by mucosal pigmentation and gastrointestinal polyps. The polyps, usually pedunculated hamartomas, are significant only for the symptoms they cause. Intramural lesions also have been described with gross microscopic features that are often interpreted as malignant. Careful evaluation may show most of these lesions to be enteritis cystica profunda. These rarely diagnosed but benign tumors have very different implications for treatment and prognosis.

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Year:  1987        PMID: 3829862     DOI: 10.1007/bf02554338

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


  4 in total

1.  Enteritis Cystica Profunda Presenting as Recurrent Sub Acute Intestinal Obstruction-NOT ALL Cases of IC Strictures are Koch's! A Case Report.

Authors:  Raviraj Jadhav; Suraj Prabhudesai; Shulmit Vaidya; Rajesh Nathani; Roy Patankar
Journal:  Indian J Surg       Date:  2012-05-12       Impact factor: 0.656

Review 2.  Enterocolitis cystica profunda lesions in a patient with unclassified ulcerative enterocolitis.

Authors:  S H Zidi; P Marteau; F Piard; B Coffin; J P Favre; J C Rambaud
Journal:  Dig Dis Sci       Date:  1994-02       Impact factor: 3.199

Review 3.  Pathology of the hereditary colorectal carcinoma.

Authors:  Zoran Gatalica; Emina Torlakovic
Journal:  Fam Cancer       Date:  2007-06-13       Impact factor: 2.375

4.  Enteritis cystica profunda with lipoma in the second portion of the duodenum: a case report.

Authors:  Beom Jin Shim; Seung Keun Park; Hee Ug Park; Tae Young Park
Journal:  J Yeungnam Med Sci       Date:  2021-06-09
  4 in total

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