Literature DB >> 1854886

Cyclosporin for hypereosinophilic syndrome.

P Zabel1, M Schlaak.   

Abstract

The idiopathic hypereosinophilic syndrome (HES) comprises a heterogeneous group of disorders with unknown pathogenesis characterized by persistent peripheral blood and bone marrow eosinophilia and eosinophil infiltrates of multiple organs, leading to severe organ dysfunction. Lymphokine-mediated T-lymphocyte control of human eosinophilic granulopoiesis is though to play a major role in the pathogenesis of HES. Treatment of this disease with cyclosporin-A (CSA) therefore appears to be sensible. We report the case of a patient with a severe HES who failed to respond adequately to glucocorticoid treatment. With additional CSA therapy, disease activity showed a favorable remission and eosinophil counts rapidly decreased to the normal range and remained normal even after reduction of the methylprednisolone dosage to 7.5 mg daily. To date his remission has continued for more than 6 months. In the meantime we have confirmed the beneficial effects of CSA in two other cases of HES. This suggests that CSA treatment is justified, at least in combination with glucocorticoids, in severe cases of HES to prevent the side effects of a long-lasting high-dose glucocorticoid therapy.

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Year:  1991        PMID: 1854886     DOI: 10.1007/bf01729838

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  7 in total

1.  A clinicopathologic correlation of the idiopathic hypereosinophilic syndrome. II. Clinical manifestations.

Authors:  R T Schooley; M A Flaum; H R Gralnick; A S Fauci
Journal:  Blood       Date:  1981-11       Impact factor: 22.113

2.  Evidence for the clonal nature of hypereosinophilic syndrome.

Authors:  M A da Silva; N Heerema; G R Schwenk; R Hoffman
Journal:  Cancer Genet Cytogenet       Date:  1988-05

Review 3.  NIH conference. The idiopathic hypereosinophilic syndrome. Clinical, pathophysiologic, and therapeutic considerations.

Authors:  A S Fauci; J B Harley; W C Roberts; V J Ferrans; H R Gralnick; B H Bjornson
Journal:  Ann Intern Med       Date:  1982-07       Impact factor: 25.391

4.  A clinicopathologic correlation of the idiopathic hypereosinophilic syndrome. I. Hematologic manifestations.

Authors:  M A Flaum; R T Schooley; A S Fauci; H R Gralnick
Journal:  Blood       Date:  1981-11       Impact factor: 22.113

5.  Therapy of the hypereosinophilic syndrome.

Authors:  J E Parrillo; A S Fauci; S M Wolff
Journal:  Ann Intern Med       Date:  1978-08       Impact factor: 25.391

6.  Immunosuppressive effects of cyclosporin A on cloned T cells.

Authors:  K C Herold; D W Lancki; R L Moldwin; F W Fitch
Journal:  J Immunol       Date:  1986-02-15       Impact factor: 5.422

7.  T lymphocyte control of human eosinophilic granulopoiesis. Clonal analysis in an idiopathic hypereosinophilic syndrome.

Authors:  A Raghavachar; S Fleischer; N Frickhofen; H Heimpel; B Fleischer
Journal:  J Immunol       Date:  1987-12-01       Impact factor: 5.422

  7 in total
  3 in total

1.  NIK prevents the development of hypereosinophilic syndrome-like disease in mice independent of IKKα activation.

Authors:  Hans Häcker; Liying Chi; Jerold E Rehg; Vanessa Redecke
Journal:  J Immunol       Date:  2012-04-02       Impact factor: 5.422

2.  [Spectrum of hypereosinophilia syndrome based on 2 clinical case reports].

Authors:  H Nolte; U Helmchen
Journal:  Med Klin (Munich)       Date:  1998-07-15

Review 3.  Hypereosinophilic syndromes.

Authors:  Florence E Roufosse; Michel Goldman; Elie Cogan
Journal:  Orphanet J Rare Dis       Date:  2007-09-11       Impact factor: 4.123

  3 in total

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