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1.
Skeletal Radiol ; 46(7): 949-956, 2017 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-28429047

RESUMEN

OBJECTIVE: To assess the long-term outcome of computed tomography-guided radiofrequency ablation (CT-guided RFA) in patients with suspected osteoid osteoma (OO). MATERIALS AND METHODS: Single-center retrospective study. Patients with clinical suspicion and imaging diagnosis of osteoid osteoma were treated by CT-guided RFA using the same device with either a 7- or 10-mm active tip electrode. Specific precautions were applied in case of articular or spinal OO. Patients were contacted by phone to evaluate the long-term outcome in terms of pain, ability to perform daily activities (including sports), and long-term complications. Success was defined as the absence of residual pain and ability to perform daily activities normally. RESULTS: From 2008 to 2015, 126 patients were treated by CT-guided RFA for OO in our institution. Mean patient age was 26.1 years (SD = 11, range 1-53); mean delay to diagnosis was 16.9 months (SD = 15.2, range 1-120). Among patients who answered the follow-up call (n = 88), the overall success rate was 94.3%: 79/88 (89.8%) had primary success of the procedure, and 4/88 (4.5%) had a secondary success (repeat-RFA after pain recurrence). Mean follow-up time was 34.6 months (SD = 24.7, range 3-90). Few complications occurred: two mild reversible peripheral nerve injuries, one brachial plexus neuropathy, one broken electrode tip fragment, and one muscular hematoma. CONCLUSION: Osteoid osteoma can be effectively and safely treated by CT-guided RFA using the presented ablation protocol. Beneficial effects of the treatment persist at long-term follow-up.


Asunto(s)
Neoplasias Óseas/cirugía , Ablación por Catéter/métodos , Osteoma Osteoide/cirugía , Tomografía Computarizada por Rayos X/métodos , Actividades Cotidianas , Adolescente , Adulto , Neoplasias Óseas/diagnóstico por imagen , Niño , Preescolar , Femenino , Humanos , Lactante , Masculino , Persona de Mediana Edad , Osteoma Osteoide/diagnóstico por imagen , Ondas de Radio , Estudios Retrospectivos , Resultado del Tratamiento
2.
Abdom Imaging ; 38(4): 858-62, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23291743

RESUMEN

Renal lymphangiomatosis is an extremely rare disease characterized by developmental malformation of the lymphatic system surrounding the kidneys. We present the case of a 22-year-old pregnant female discovered because of worsening. Ultrasound, computed tomography, and magnetic resonance imaging studies were performed. An 18 × 11 × 10 cm voluminous cystic subcapsular lesion compressing the left kidney and subcapsular cysts of the right kidney were found. After the delivery, marsupialization was performed and the pathological analysis confirmed the diagnosis of lymphangiomatosis. A review of the literature is proposed.


Asunto(s)
Diagnóstico por Imagen , Neoplasias Renales/diagnóstico , Neoplasias Renales/patología , Linfangioleiomiomatosis/diagnóstico , Linfangioleiomiomatosis/patología , Diagnóstico Diferencial , Endotelio Vascular/patología , Femenino , Humanos , Neoplasias Renales/diagnóstico por imagen , Linfangioleiomiomatosis/diagnóstico por imagen , Imagen por Resonancia Magnética , Embarazo , Complicaciones del Embarazo/diagnóstico , Ultrasonografía , Adulto Joven
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