Literature DB >> 7640191

Hypereosinophilic syndrome.

K M Leiferman1.   

Abstract

The hypereosinophilic syndrome is a multisystem syndrome characterized by peripheral blood eosinophilia and eosinophil infiltration of bone marrow, heart, and other organs. The syndrome is associated with cardiac, hematological, pulmonary, neurological, and cutaneous involvement and, if untreated, has a high fatality rate. Criteria for the diagnosis of hypereosinophilic syndrome include (1) peripheral blood eosinophilia with eosinophil counts greater than 1,500/microL for at least 6 months; (2) no evidence of parasitic, allergic, or other known causes of eosinophilia; and (3) presumptive signs and symptoms of multiple organ involvement. Cutaneous manifestations occur commonly but are not diagnostic either clinically or histologically, although the presence of angioedema is a favorable prognostic sign. Because eosinophils are thought to mediate important pathogenic effects, treatment is aimed at controlling peripheral blood eosinophilia.

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Year:  1995        PMID: 7640191     DOI: 10.1016/s1085-5629(05)80007-0

Source DB:  PubMed          Journal:  Semin Dermatol        ISSN: 0278-145X


  3 in total

1.  The murine eosinophil peroxidase gene (Epx) maps to chromosome 11.

Authors:  K L Denzler; W J Levin; J J Lee; N A Lee
Journal:  Mamm Genome       Date:  1997-05       Impact factor: 2.957

2.  Inhibition of NF-κB signaling retards eosinophilic dermatitis in SHARPIN-deficient mice.

Authors:  Yanhua Liang; Rosemarie E Seymour; John P Sundberg
Journal:  J Invest Dermatol       Date:  2010-09-02       Impact factor: 8.551

Review 3.  [Allergy-associated colitis. Characterization of an entity and its differential diagnoses].

Authors:  Susanna Müller; D Schwab; T Aigner; T Kirchner
Journal:  Pathologe       Date:  2003-01-22       Impact factor: 1.011

  3 in total

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