Literature DB >> 1633365

Allergic granulomatosis and angiitis with severe cardiac disease: a case in which cardiac function was extremely improved by long-term steroid therapy.

N Takahashi1, M Horita, M Tatsukawa, T Maeda, M Seike, T Saikawa, R Takaki, T Mori, S Yokoyama.   

Abstract

A 38-year-old man with a history of bronchial asthma developed marked eosinophilia, mononeuritis multiplex and transient pulmonary infiltration. Pathological findings from the lung and nerve biopsy were helpful in determining the diagnosis as allergic granulomatosis and angiitis (AGA). Echocardiogram indicated dilation of the left ventricle with impaired systolic contraction. Coronary arteriography demonstrated significant stenosis only in the peripheral segment of the circumflex artery. After 1 year of corticosteroid therapy, echocardiogram revealed improvement of left ventricular contractility evaluated by ejection fraction (from 28% to 67%). To our knowledge, no previous reports have described amelioration of severe cardiac lesions during long-term steroid treatment in patients with AGA.

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Year:  1992        PMID: 1633365     DOI: 10.2169/internalmedicine.31.534

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  3 in total

1.  Cardiac involvement as the main presenting feature in eosinophilic granulomatosis with polyangiitis.

Authors:  Neil McAleavey; Auleen Millar; Adrian Pendleton
Journal:  BMJ Case Rep       Date:  2013-07-12

2.  Evolution to dilated cardiomyopathy from acute eosinophilic pancarditis in Churg-Strauss syndrome.

Authors:  F Terasaki; T Hayashi; Y Hirota; M Okabe; M Suwa; H Deguchi; Y Kitaura; K Kawamura
Journal:  Heart Vessels       Date:  1997       Impact factor: 2.037

3.  Churg-Strauss syndrome following cessation of allergic desensitization vaccination: a case report.

Authors:  Mohammad Reza Masjedi; Saeid Fallah Tafti; Ali Cheraghvandi; Nader Fayazi; Firouzeh Talischi; Bahareh Mokri
Journal:  J Med Case Rep       Date:  2010-06-22
  3 in total

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