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Significant fibrosis after radiation therapy in a patient with Marfan syndrome
Radiation Oncology Journal ; : 208-212, 2014.
Artigo em Inglês | WPRIM | ID: wpr-112697
ABSTRACT
Marfan syndrome is one of the collagen vascular diseases that theoretically predisposes patients to excessive radiation-induced fibrosis yet there is minimal published literature regarding this clinical scenario. We present a patient with a history of Marfan syndrome requiring radiation for a diagnosis of a right brachial plexus malignant nerve sheath tumor. It has been suggested that plasma transforming growth factor beta 1 (TGF-beta1) can be monitored as a predictor of subsequent fibrosis in this population of high risk patients. We therefore monitored the patient's TGF-beta1 level during and after treatment. Despite maintaining stable levels of plasma TGF-beta1, our patient still developed extensive fibrosis resulting in impaired range of motion. Our case reports presents a review of the literature of patients with Marfan syndrome requiring radiation therapy and the limitations of serum markers on predicting long-term toxicity.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Plasma / Doenças Vasculares / Fibrose / Plexo Braquial / Biomarcadores / Amplitude de Movimento Articular / Fator de Crescimento Transformador beta / Colágeno / Diagnóstico / Fator de Crescimento Transformador beta1 Tipo de estudo: Estudo diagnóstico / Estudo prognóstico Limite: Humanos Idioma: Inglês Revista: Radiation Oncology Journal Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Plasma / Doenças Vasculares / Fibrose / Plexo Braquial / Biomarcadores / Amplitude de Movimento Articular / Fator de Crescimento Transformador beta / Colágeno / Diagnóstico / Fator de Crescimento Transformador beta1 Tipo de estudo: Estudo diagnóstico / Estudo prognóstico Limite: Humanos Idioma: Inglês Revista: Radiation Oncology Journal Ano de publicação: 2014 Tipo de documento: Artigo