Digestive system

• digestive duplication cyst
  15 October 2003

  digestive duplication cysts

• Hirschsprung disease
  6 October 2003

  Hirschsprung’s disease, congenital intestinal aganglionosis, digestive aganglionnosis; digestive aganglionoses PO1 PO2
  Definition: Aganglionic megacolon is associated with congenital absence of intrinsic ganglion cells in the myenteric (Auerbach) and submucosal (Meissner) plexuses of the gastrointestinal tract. The disorder is genetically heterogeneous.
  Digital cases
  HPC:90 : rectal mucosa biopsies
  HPC:98 : rectal mucosa biopsies
  HPC:151 : Hirschsprung disease - Rectal (...)

• digestive vascular anomalies
  3 October 2003

  digestive vascular lesions
  Types
  arterio-venous malformations angiodysplasia Dieulafoy lesion
  venous ectasias (multiple phlebectasias and haemorroids )
  teleangiectasias hereditary hemorrhagic teleangiectasia (HHT) Turner syndrome systemic sclerosis
  haemangioma
  angiosarcoma
  disorders of connective tissue affecting blood vessels pseudoxanthoma elasticum Ehlers-Danlos’s disease
  See also
  vascular anomalies
  vascular (...)

• eosinophilic enterocolitis
  3 October 2003

  eosinophilic ileocolitis

• eosinophilic gastroenteritis
  3 October 2003

  Definition: Eosinophilic gastroenteritis is a heterogeneous lesionnal syndrome characterized by eosinophilic inflammation of the gastrointestinal tissues.
  Eosinophilic gastroenteritis is a rare condition characterized by recurrent eosinophilic infiltration of portions of the GI tract and presenting with nonspecific GI symptoms in association with peripheral eosinophilia. Its etiology and pathogenesis remain unclear and its symptoms overlap with many GI and systemic diseases.
  Eosinophilic (...)

• cow milk allergy
  3 October 2003

  cow milk hypersensitivity, CMA, cow milk allergy

• eosinophilic granulomatous enterocolitis
  3 October 2003

  Etiology
  Strongyloides stercoralis eosinophilic granulomatous enterocolitis (#8619425#)

• granulomatous enterocolitis
  3 October 2003

  Classification
  eosinophilic granulomatous enterocolitis
  Etiology (exemples)
  Crohn disease
  tuberculous enterocolitis
  digestive CGD (chronic grnaulomatous disease)
  Hermansky-Pudlak syndrome

• digestive Crohn disease
  29 September 2003

  Localization
  gastric Crohn disease (Crohn gastritis)
  intestinal Crohn disease (Crohn enteritis)
  ileal Crohn disease (Crohn ileitis)
  colonic Crohn disease (Crohn colitis)
  rectal Crohn disease (Crohn rectitis)
  anal Crohn disease (Crohn proctitis)
  Susceptibility
  Locus IBD1
  Locus IBD2
  Locus IBD3
  Locus IBD4
  Locus IBD5 - 5q31 cytokine gene cluster
  Locus IBD6
  Locus CARD15
  vitamin D receptor gene polymorphism (#10896912#)
  Videos
  Ileal Crohn disease by Washington (...)

• hereditary mixed polyposis syndrome
  26 September 2003

  HMPS, CRAC1,
  The hereditary mixed polyposis syndrome (HMPS) is characterized by atypical juvenile polyps ( MIM.174900 ), colonic adenomas, and colorectal carcinomas. Many polyps are mixed in pattern.
  The term ‘mixed’ relates both to the variety of polyps observed in this condition and the presence of polyps with features reminiscent of more than one of the classic types of colorectal polyp.
  Synopsis
  Hereditary syndrome characterized by the appearance of various types of polyps, many of (...)

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