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1.
Reumatismo ; 76(1)2024 Mar 22.
Artigo em Inglês | MEDLINE | ID: mdl-38523583

RESUMO

OBJECTIVE: Melorheostosis is a rare, non-hereditary, benign bone disease characterized by abnormal bone growth. Generally, melorheostosis develops during childhood or adolescence and progresses gradually over time. This disease represents a true challenge to the physician because of its variability due to location, extension of the affected bone, and involvement of associated soft tissue. Pain management, physical therapy, and surgery may be recommended, depending on the individual case. This review aims to get an overview of the latest evidence relating to epidemiology, clinical and radiographic characteristics, diagnosis, and possible therapeutic strategies for melorheostosis and describe our experience through a clinical case. METHODS: We designed a comprehensive literature search on melorheostosis in MEDLINE (via Pubmed) up to April 2023 and reviewed reports published in international journals. RESULTS: The purpose is to highlight the importance of a multidisciplinary approach in the management of a rare disease such as melorheostosis. We discuss the role of different physicians, including genetists, rheumatologists, physiatrists, physical therapists, and orthopedic surgeons, in providing accurate diagnoses and effective treatments. We conducted a comprehensive review of the literature on the treatment of melorheostosis to support these findings. In addition, the article presents a case study of a patient suffering from melorheostosis, focusing on difficulties in reaching a correct diagnosis and attempts towards conservative and surgical interventions. The patient underwent hip arthroplasty, and the final result was an improvement in function and a reduction in pain. CONCLUSIONS: Managing melorheostosis can be challenging, and there is no standardized treatment for this condition at the moment.


Assuntos
Melorreostose , Adolescente , Humanos , Melorreostose/complicações , Melorreostose/cirurgia , Melorreostose/diagnóstico , Dor , Manejo da Dor , Resultado do Tratamento , Doenças Raras
2.
Pulmäo RJ ; 13(4): 282-285, 2004. ilus
Artigo em Português | LILACS | ID: lil-642183

RESUMO

O objetivo desse estudo foi fazer uma revisão dos sinais clínicos e radiológicos de um caso atípico de melorreostose: uma mulher de 62 anos com alterações hiperostóticas irregular, de envolvimento bilateral, nos ossos raramente afetados como clavícula, escápula, costelas e crânio. Adicionalmente, a paciente tem múltiplos nevos e o diagnóstico foi feito devido a um quilotórax resistente a terapia e com evolução rápida para insuficiência respiratória.


Assuntos
Humanos , Feminino , Idoso , Hiperostose , Melorreostose/complicações , Melorreostose/diagnóstico , Derrame Pleural , Quilotórax/terapia , Técnicas e Procedimentos Diagnósticos , Osteosclerose , Sinais e Sintomas
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