Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros










Intervalo de ano de publicação
2.
Reumatol. clín. (Barc.) ; 1(2): 131-133, jul.-ago. 2005. ilus
Artigo em Espanhol | IBECS | ID: ibc-77506

RESUMO

La paquidermodactilia (PDD) es una forma rara y benigna de fibromatosis digital. Se caracteriza por un engrosamiento asintomático de los tejidos blandos en las caras laterales de las articulaciones interfalángicas proximales de las manos y a veces puede confundirse con algunas enfermedades reumáticas. Los cambios visibles en la resonancia magnética no han sido descritos hasta ahora en la bibliografía médica. Presentamos un caso de PDD en un varón de 19 años y describimos los hallazgos radiológicos en la radiografía simple y en la resonancia magnética. Asimismo, se discute brevemente la PDD(AU)


Pachydermodactyly (PDD) is a rare, benign form of digital fibromatosis characterized by an asymptomatic soft-tissue swelling affecting the skin of the lateral aspects of the proximal interphalangeal joints of the fingers, and sometimes can be misdiagnosed with some rheumatic conditions. Magnetic resonance images changes have not been described in any of the case reports in the literature. We report here a case of PDD in a 19-year-old male and we describe its findings on X-ray and magnetic resonance images. We briefly discuss PDD(AU)


Assuntos
Humanos , Masculino , Adulto , Fibroma/etiologia , Articulações dos Dedos/fisiopatologia , Diagnóstico Diferencial , Corticosteroides/uso terapêutico
3.
Reumatol Clin ; 1(2): 131-3, 2005 Aug.
Artigo em Espanhol | MEDLINE | ID: mdl-21794249

RESUMO

Pachydermodactyly (PDD) is a rare, benign form of digital fibromatosis characterized by an asymptomatic soft-tissue swelling affecting the skin of the lateral spects of the proximal interphalangeal joints of the fingers, and sometimes can be misdiagnosed with some rheumatic conditions. Magnetic resonance images changes have not been described in any of the case reports in the literature. We report here a case of PDD in a 19-year-old male and we describe its findings on X-ray and magnetic resonance images. We briefly discuss PDD.

5.
J Rheumatol ; 18(9): 1368-71, 1991 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-1757939

RESUMO

We assessed muscle pathology in 30 patients with ankylosing spondylitis (AS) and 22 controls to assess if skeletal muscle is affected primarily by the inflammatory process of the disease. Investigations included a questionnaire on musculoskeletal discomfort, physical exercises, dynamometric measurements, EMG, and biopsy of the quadriceps muscle. Symptoms of muscular weakness were related with enthesopathic activity index. Plasma CK was higher in patients than in controls. A myopathic EMG pattern was found in 46.4% patients. Histological changes were found in 66% and did not correlate with symptomatology. Patients with AS with clinical muscular manifestations probably have intense enthesopathic inflammatory activity. It is suggested that muscles are secondarily affected as a consequence of pain inhibition and reduced activity.


Assuntos
Músculos/patologia , Espondilite Anquilosante/patologia , Adolescente , Adulto , Idoso , Biópsia , Eletromiografia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Músculos/fisiologia , Dor , Estudos Prospectivos , Espondilite Anquilosante/epidemiologia , Espondilite Anquilosante/fisiopatologia , Inquéritos e Questionários
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...