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1.
Radiology ; 196(2): 353-61, 1995 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-7617844

RESUMO

PURPOSE: To assess the clinical success and short-term patency of the Wallstent endoprosthesis in the treatment of superior vena cava (SVC) syndrome. MATERIALS AND METHODS: Twenty-one 14-mm-diameter endoprostheses were implanted in 15 patients (mean age, 60 years) treated for SVC syndrome due to malignant compression (n = 14) or postirradiation fibrotic stenosis (n = 1) of the SVC. RESULTS: Immediate technical success was achieved in all patients. Two early complications occurred: retroperitoneal hemorrhage due to venous iliac tear and early stent thrombosis. In the 14 patients without early stent occlusion, stent placement resulted in complete relief of SVC syndrome; clinical success was 93%. SVC syndrome did not recur from 1 to 14 months, until the patient died (n = 11) or until the end of the study (n = 3). Helical CT showed a patent stent in five patients, respectively, at 3, 6, 8, 10, and 11 months. CONCLUSION: SVC stent placement has good clinical results and a high patency rate at short-term follow-up in patients with SVC syndrome.


Assuntos
Stents , Síndrome da Veia Cava Superior/terapia , Carcinoma Pulmonar de Células não Pequenas/complicações , Desenho de Equipamento , Feminino , Seguimentos , Humanos , Neoplasias Pulmonares/complicações , Masculino , Pessoa de Meia-Idade , Radiografia Intervencionista/métodos , Aço Inoxidável , Stents/efeitos adversos , Síndrome da Veia Cava Superior/diagnóstico por imagem , Síndrome da Veia Cava Superior/etiologia , Fatores de Tempo , Resultado do Tratamento , Grau de Desobstrução Vascular/fisiologia
2.
Eur Respir J ; 7(6): 1194-6, 1994 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-7925894

RESUMO

Cardiac angiosarcoma is a rare tumour with very poor prognosis especially in patients with metastatic disease. We present the case of a 43 year old patient with angiosarcoma revealed by open lung biopsy for multiple pulmonary metastases. Cardiac symptoms were limited to a moderate pericarditis and no echocardiographic sign of heart tumour was observed. The clinical outcome was rapidly fatal despite chemotherapy. The cardiac primary tumour was diagnosed at autopsy. We emphasize the difficulties of diagnosing cardiac angiosarcoma and confirm the limited value of echocardiography for this diagnosis.


Assuntos
Neoplasias Cardíacas/diagnóstico , Hemangiossarcoma/diagnóstico , Hemangiossarcoma/secundário , Neoplasias Pulmonares/secundário , Adulto , Evolução Fatal , Humanos , Masculino
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