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Classic/amyopathic dermatomyositis.


 
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1. Title Title of document Classic/amyopathic dermatomyositis.
 
2. Creator Author's name, affiliation, country A P Vilas; Serviço de Medicina Interna e Gastroenterologia, Hospital Pulido Valente, Lisboa.; Portugal
 
2. Creator Author's name, affiliation, country T Fiúza; Portugal
 
3. Subject Discipline(s)
 
3. Subject Keyword(s)
 
4. Description Abstract Dermatomyositis (DM) is an inflammatory myopathy characterized by a typical cutaneous rash and proximal weakness. DM results from endothelium deposition of the complement membranolytic attack complex C5b-9, followed by inflammation. It is thus possible to have cases of DM with the typical rash, but with no associated myositis--amiopathic DM. DM represents a higher risk of association with malignancy and sometimes behaves as a paraneoplastic syndrome. As DM can be the alarm sign, once diagnosed, exclusion of malignancy should be done. In this article we also discuss the treatment and prognosis of dermatomyositis, according to the literature.
 
5. Publisher Organizing agency, location Ordem dos Médicos
 
6. Contributor Sponsor(s)
 
7. Date (YYYY-MM-DD) 2000-12-30
 
8. Type Status & genre article
 
8. Type Type
 
9. Format File format PDF (Português)
 
10. Identifier Uniform Resource Identifier https://actamedicaportuguesa.com:443/revista/index.php/amp/article/view/1801
 
10. Identifier Digital Object Identifier (DOI) http://dx.doi.org/10.20344/amp.1801
 
11. Source Title; vol., no. (year) Acta Médica Portuguesa; Vol 13, No 5-6 (2000): Setembro-Dezembro
 
12. Language English=en
 
14. Coverage Geo-spatial location, chronological period, research sample (gender, age, etc.)
 
15. Rights Copyright and permissions Copyright (c)