Literature DB >> 3450209

[Myasthenia in children: long-term course].

H Descamps1, J Bataille, B Estournet, A Barois.   

Abstract

Twenty three children with myasthenia were followed up in our Department for 10 years. There were no familial forms of the disease; there were no patients with the pure ophthalmic form but 61 p. 100 of patients had serious respiratory disease. Steroid therapy was possible in 10 cases: in 4 patients under 15 years of age, short courses of steroids were ineffective; in 6 patients over the age of 15, long term steroid therapy resulted in some improvement but cortico-dependence developed in 4 cases. One child responded to treatment with veinoglobulin (R). Sixteen children underwent thymectomy; the symptoms in the 7 non-thymectomized patients were equivalent. The myasthenic syndrome was stable or worsened in 75 p. 100 of cases after thymectomy; only 56 p. 100 of children improved 2 years after surgery. The incidence of complete remission was the same in the children undergoing thymectomy and in those not treated surgically at 7 years after thymectomy. Our attitude is therefore not to refer myasthenic children for routine thymectomy and to avoid steroid therapy whenever possible.

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Mesh:

Year:  1987        PMID: 3450209

Source DB:  PubMed          Journal:  Ann Med Interne (Paris)        ISSN: 0003-410X


  1 in total

1.  Immunosuppressive treatment for juvenile myasthenia gravis.

Authors:  B Badurska; B Ryniewicz; H Strugalska
Journal:  Eur J Pediatr       Date:  1992-03       Impact factor: 3.183

  1 in total

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