Hypereosinophilic syndrome: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Howard C. Berkowitz
(New page: {{subpages}} <!-- Text is transcluded from the BASEPAGENAME/Definition subpage-->)
 
imported>Howard C. Berkowitz
mNo edit summary
 
(4 intermediate revisions by the same user not shown)
Line 1: Line 1:
{{subpages}}
{{subpages}}
<!-- Text is transcluded from the BASEPAGENAME/Definition subpage-->
A heterogeneous group of disorders with the common feature of prolonged [[eosinophilia]] of unknown cause and associated organ system dysfunction, including the [[heart]], [[central nervous system]], [[kidney]]s, [[lung]]s, [[gastrointestinal tract]], and [[skin]]. {<ref name=MeSH>{{MeSH}}</ref> There is an [[idiopathic]] form not otherwise characterized, but the group also includes [[Churg-Strauss syndrome]], and a group of  Eosinophil-Associated Gastrointestinal Disorders (EGID):<ref>{{citation
| url = http://www.apfed.org/egid.htm
| publisher = American Partnership for Eosinophilic Disorders
| title = About EGID}}</ref>
*Eosinophilic Esophagitis (EE): high numbers of eosinophils occurring in the esophagus.    *Eosinophilic Esophagitis
*Eosinophilic Gastritis (EG): high numbers of eosinophils in the stomach.
*Eosinophilic Gastroenteritis (EGE): affects the stomach and small intestine.
*Eosinophilic Colitis (EC): describes the occurrence of high numbers of eosinophils in the large intestine.
 
The diagnosis requires:<ref name=eMed-Derm-Over>{{citation
| title = eMedicine Specialties > Dermatology > Allergy & Immunology > Hypereosinophilic Syndrome: Introduction
| author =  Noah S Scheinfeld, Felix Urman
| date = 1 February 2010
| journal = eMedicine
| url = http://emedicine.medscape.com/article/1051555-overview}}</ref>
*a peripheral eosinophil count of greater than 1.5 per microliter for longer than 6 months
*evidence of organ involvement, thus excluding benign eosinophilia
*an absence of other causes of eosinophilia, such as parasite infestation (most common cause of eosinophilia worldwide), allergy (most common cause of eosinophilia in the United States), malignancy, and collagen-vascular disease.
 
A support group reports three patients with the idiopathic form. <ref>{{citation
| url = http://www.hesyndrome.com/about.html
|publisher =  Hyper Eosinophilia Syndrome (HES)
| title = Idiopathic Eosinophilia}}</ref>
==Pathology==
There is a massive increase in the number of  [[eosinophil]]s in the blood, mimicking [[leukemia]], and extensive eosinophilic infiltration of the various organs. <ref name=MeSH/> Eosinophil production is known to be stimulated by [[interleukin]]s.<ref>{{citation
| journal = International Immunology
| year = 2010
  | volume = 22 | issue = 6 | pages = 479-489| doi= 10.1093/intimm/dxq035
| title = Contribution of IL-33 to induction and augmentation of experimental allergic conjunctivitis
| author = Saori Matsuba-Kitamura ''et al''
| url =http://intimm.oxfordjournals.org/cgi/content/full/22/6/479
}}</ref>
==References==
{{reflist|2}}

Latest revision as of 11:33, 6 August 2010

This article is developing and not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.

A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. {[1] There is an idiopathic form not otherwise characterized, but the group also includes Churg-Strauss syndrome, and a group of Eosinophil-Associated Gastrointestinal Disorders (EGID):[2]

  • Eosinophilic Esophagitis (EE): high numbers of eosinophils occurring in the esophagus. *Eosinophilic Esophagitis
  • Eosinophilic Gastritis (EG): high numbers of eosinophils in the stomach.
  • Eosinophilic Gastroenteritis (EGE): affects the stomach and small intestine.
  • Eosinophilic Colitis (EC): describes the occurrence of high numbers of eosinophils in the large intestine.

The diagnosis requires:[3]

  • a peripheral eosinophil count of greater than 1.5 per microliter for longer than 6 months
  • evidence of organ involvement, thus excluding benign eosinophilia
  • an absence of other causes of eosinophilia, such as parasite infestation (most common cause of eosinophilia worldwide), allergy (most common cause of eosinophilia in the United States), malignancy, and collagen-vascular disease.

A support group reports three patients with the idiopathic form. [4]

Pathology

There is a massive increase in the number of eosinophils in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs. [1] Eosinophil production is known to be stimulated by interleukins.[5]

References

  1. 1.0 1.1 Anonymous (2024), Hypereosinophilic syndrome (English). Medical Subject Headings. U.S. National Library of Medicine.
  2. About EGID, American Partnership for Eosinophilic Disorders
  3. Noah S Scheinfeld, Felix Urman (1 February 2010), "eMedicine Specialties > Dermatology > Allergy & Immunology > Hypereosinophilic Syndrome: Introduction", eMedicine
  4. Idiopathic Eosinophilia, Hyper Eosinophilia Syndrome (HES)
  5. Saori Matsuba-Kitamura et al (2010), "Contribution of IL-33 to induction and augmentation of experimental allergic conjunctivitis", International Immunology 22 (6): 479-489, DOI:10.1093/intimm/dxq035