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Arquivos de Neuro-Psiquiatria

Print version ISSN 0004-282X

Arq. Neuro-Psiquiatr. vol.26 no.3 São Paulo Sept. 1968

http://dx.doi.org/10.1590/S0004-282X1968000300003 

Mioscleroses

 

Myosclerosis

 

 

José Antonio Levy

Professor assistente de Clínica Neurológica na Faculdade de Medicina da Universidade de São Paulo (Prof. Adherbal Tolosa)

 

 


RESUMO

São apresentados os casos de 7 pacientes miopatas com retrações fibrotendinosas precoces. O autor é de opinião que este tipo de afecção não constitui uma unidade nosológica bem definida e compara suas observações com outras referidas na literatura médica citando ,entre outras, a miopatia esclerosa limitante, a esclerose muscular generalizada, as mioscleroses heredo-familiares, as miosites fibrosas, a miosclerose senil, a mesenquimose displásica e a atrogripose.


SUMMARY

The cases of 7 myopathic patients with precocious fibrotendinous retractions p.re reported. The author suggests that this type of affection does not constitute a well defined nosological entity in itself. He discusses the bibliographic references on the subject, considering limiting sclerotic myopathies, generalized muscular sclerosis, heredofamiliar myosclerosis, fibrous myositis, senile myosclerosis, dysplastic mesenchymosis and arthrogryposis.


 

 

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REFERÊNCIAS

1. BOGAERT, L. Van & RADERMECKER, M. A. — De quelques affections musculaires primitives en dehors des myopathies. Acta neurol. psychiat. belg. 54:1-28, 1954.         [ Links ]

2. BOGAERT, L. Van; BESSA, J. S. & NUNES VICENTE, A. — Sur une affection musculaire congénitale à evolution lentement favorable caractérisée par une "eirrhose" musculaire à depots protéiniques (réticulose musculaire?). Acta neurol. psychiat. belg. 62:973-983, 1962.         [ Links ]

3. CORDIER, J.; LOWENTHAL, A.; RADERMECKER, M. A. & BOGAERT, L. Van — Sur une forme congénitale et héréditaire de sclerose musculaire généralisée. Acta neurol. psychiat. belg. 52:422-432, 1952.         [ Links ]

4. FURTADO, D.; NEVES DA SILVA & CHICHORRO, V. — Polymyosite sclérosante segmentaire. Rev. Neurol. 103:572-582, 1960        [ Links ]

5. GARCIN, R.; LAPRESLE, J.; GRUNER, J. & SCHERIER, J. — Les polymyosites. Rev. Neurol. 92:465-510, 1955.         [ Links ]

6. GAREISO, A. & ESCARDÓ, F. — Manual de Neurologia Infantil. Livraria Editora El Ateneo, Buenos Aires, 1944, pp. 11 a 31.         [ Links ]

7. HARIGA, J.; LOWENTHAL, A. & GUAZZI, G. C. — Nosological place and correlations of artrogryposis "sensu stricto". Acta neurol. psychiat. belg. 63: 766-793, 1963.         [ Links ]

8. HAUPTMANN, A. & TANNAHAUSER, S. J. — Muscular shortenings and dystrophies. Arch. Neurol. Psychiat. 46:654-664, 1941.         [ Links ]

9. LEVY, J. A. — Contribuição para o diagnóstico diferencial da distrofia muscular progressiva. Arq. Neuro-Psiquiat. (São Paulo), 22:73-104, 1964.         [ Links ]

10. LOWENTHAL, A. — Sur une forme congénitale et familiale de sclerose musculaire généralisée avec blepharoptose. Acta neurol. psychiat. belg. 52:141-155, 1952.         [ Links ]

11. LOWENTHAL, A. — Un group hérédodégénératif nouveau: les myoscleroses hérédofamiliales. Acta neurol. psychiat. belg. 54:155-165, 1954.         [ Links ]

12. POCH, G. F. & MONTEVECCHIO, B. — Miopatia esclerosa limitante de Cestan y Lejonne. Rev. neurol. Buenos Aires 14:29-38, 1956.         [ Links ]

13. SHY, G. M. & MAGGE, K. R. — A new congenital non progressive myopathy. Brain 79:610, 1950.         [ Links ]

14. SCHMIDT-PETER, P. Von & LÜDERS, C. J. — Uber eine Patienten mit lo-r dose Kontraktur der gesamten Wirbelsáule bei progredienter Muskelatrophie und interstitieller Fibrolipomatose. Ein Beitrag zum Problem der dysplastichen mesenchymosen. Helv. paediat. Acta 20:101-117, 1965. Resumo inMuscular Dystrophy Abstracts 10, 3, 1966.         [ Links ]

15. VUIA, O. & STANESCO, A. — Maladies conjonctives dégénératives: myostierose, lipomatose symetrique et myosite ossificante progressive. J. Neurol. ScL 3:473-489, 1966.         [ Links ]

16. WALTON, J. N. — Two cases of myopathy limited to the quadriceps. J. Neurol. Neuiosurg. Psychiat. 19:106-108, 1956.         [ Links ]

17. ZARATE, O. & ETCHEBERRIT, J. M. — Miositis crónica hereditaria. Acta neuro-psiquat. argent. 5:305-312, 1959.         [ Links ]

 

 

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