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1.
Clinics in Orthopedic Surgery ; : 439-442, 2014.
Artículo en Inglés | WPRIM | ID: wpr-223880

RESUMEN

BACKGROUND: Aggressive fibromatosis is a rare but invasive tumor infiltrating widely between fascia and muscle fibers. It has a high tendency to be locally recurrent despite complete resection. Effectiveness of adjuvant treatment for aggressive fibromatosis including radiotherapy, pharmacological agents, hormonal treatments, and chemotherapy have been previously reported. The purpose of this article was to collect and analyze all information regarding the effectiveness and side effects of oral methotrexate in aggressive fibromatosis. METHODS: From 2005 to 2011, eleven patients with aggressive fibromatosis treated with oral methotrexate at our institution were analyzed in this study. Oral methotrexate was administered once per week at 10 mg per week. Authors collected information about effectiveness concerning cases of local recurrence and metastasis. RESULTS: Eleven patients had remission, two patients had local recurrence. Fatal complications or toxicity were not observed. CONCLUSIONS: Oral methotrexate given at this dose and schedule was considered as a useful treatment in primary inoperable fibromatosis and recurrent fibromatosis.


Asunto(s)
Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Adulto Joven , Administración Oral , Antimetabolitos Antineoplásicos/administración & dosificación , Fibromatosis Agresiva/tratamiento farmacológico , Metotrexato/administración & dosificación , Recurrencia Local de Neoplasia/tratamiento farmacológico , Estudios Retrospectivos
2.
The Journal of the Korean Orthopaedic Association ; : 319-323, 2013.
Artículo en Coreano | WPRIM | ID: wpr-656136

RESUMEN

Sprengel's deformity is characterized by the congenital migration of the scapula superiorly in relation to the thoracic cage. Other congenital anomalies, such as Klippel-Feil syndrome, may occur in combination with Sprengel's deformity. We report on a case of Sprengel's deformity with a huge bilateral omovertebrae, which was combined with the clinical features of Klippel-Feil syndrome, including cervical fusion, short neck, low posterior hairline, and limitation of neck motion. However, no other deformities or functional defects were observed.


Asunto(s)
Anomalías Congénitas , Síndrome de Klippel-Feil , Cuello , Escápula , Articulación del Hombro
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