Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 10 de 10
Filtrar
1.
Arch Bronconeumol ; 36(10): 594-6, 2000 Nov.
Artigo em Espanhol | MEDLINE | ID: mdl-11149203

RESUMO

Aorto-bronchial fistula is a rare but associated with a height rare of mortality. Although most reported cases are secondary to infectious aneurysms, cases arising after surgery to correct congenital cardiovascular abnormalities have recently been described. We report the case of a 41-year-old patient with recurrent hemoptysis and a history of Fallot's tetralogy corrected in childhood. Given such a case of hemoptysis in a patient with a history of cardiovascular surgery, the correct diagnostic approach includes fiberoptic bronchoscopy, helicoidal CAT and/or NMR, and aortography. Diagnostic confirmation should be followed soon by corrective surgery.


Assuntos
Fístula Brônquica/complicações , Hemoptise/etiologia , Complicações Pós-Operatórias , Tetralogia de Fallot/cirurgia , Fístula Vascular/complicações , Adulto , Fístula Brônquica/diagnóstico por imagem , Hemoptise/diagnóstico por imagem , Humanos , Masculino , Complicações Pós-Operatórias/diagnóstico por imagem , Artéria Pulmonar/diagnóstico por imagem , Radiografia , Reoperação , Artéria Subclávia/diagnóstico por imagem , Tetralogia de Fallot/diagnóstico por imagem , Fístula Vascular/diagnóstico por imagem
2.
An Med Interna ; 15(12): 656-7, 1998 Dec.
Artigo em Espanhol | MEDLINE | ID: mdl-9972602

RESUMO

Infrahepatic interruption of the inferior cava vein, is a rare congenital anomaly, usually associated with congenital heart and abdominal diseases. The systemic venous flow is accommodated by the dilated azygos. This dilated azygos arch accounts for the right paratracheal or mediastinal mass, and may be misinterpreted as a neoplasm. We report a case with this congenital vascular anomaly, associated with another of tracheobronchial tree.


Assuntos
Veia Ázigos/patologia , Pneumopatias/diagnóstico , Veia Cava Inferior/anormalidades , Diagnóstico Diferencial , Dilatação Patológica , Humanos , Pneumopatias/diagnóstico por imagem , Masculino , Pessoa de Meia-Idade , Radiografia Torácica , Tomografia Computadorizada por Raios X
3.
An Med Interna ; 11(12): 598-600, 1994 Dec.
Artigo em Espanhol | MEDLINE | ID: mdl-7734668

RESUMO

The epitheloid hemangioendothelioma (EH) is a rare tumor of vascular origin, which exceptionally manifestates as a mediastinic mass. We present a new case of location at the upper cava vein and we review the clinical, histological and therapeutic characteristics of the EH.


Assuntos
Hemangioendotelioma Epitelioide , Neoplasias do Mediastino , Hemangioendotelioma Epitelioide/diagnóstico , Humanos , Masculino , Neoplasias do Mediastino/diagnóstico , Pessoa de Meia-Idade
4.
Rev. patol. respir ; 20(3): 91-93, jul.-sept. 2017. ilus
Artigo em Espanhol | IBECS (Espanha) | ID: ibc-167630

RESUMO

El secuestro pulmonar es una malformación congénita poco frecuente, generalmente asintomática hasta que la lesión se infecta, debutando entonces como infecciones respiratorias de repetición. El diagnóstico se confirma mediante pruebas de imagen que permitan objetivar el tejido pulmonar no funcionante irrigado por circulación sistémica. El tratamiento de elección es la resección quirúrgica con ligadura de los vasos nutricios


Pulmonary sequestration is a rare congenital abnormality. Most of them are asymptomatic but they can appear as recurrent respiratory infections. Radiological tests bring to light a non functioning mass of lung that receives its arterial blood supply from the systemic circulation. Treatment is made with a surgical resection by bonding the vascular supply


Assuntos
Humanos , Masculino , Adulto , Sequestro Broncopulmonar/complicações , Infecções Respiratórias/complicações , Anormalidades do Sistema Respiratório/diagnóstico por imagem , Sequestro Broncopulmonar/cirurgia , Pneumonectomia , Cirurgia Torácica Vídeoassistida
6.
Rev. esp. patol. torac ; 28(5): 280-282, dic. 2016. ilus
Artigo em Espanhol | IBECS (Espanha) | ID: ibc-159718

RESUMO

La dilatación aneurismática de la arteria pulmonar es una patología rara y clínicamente inespecífica, por lo que el diagnóstico se basa en pruebas de imagen, como la TC o la angiorresonancia. Puede ser idiopática (menos frecuente) cuando la etiología es indeterminada o secundaria a diversas patologías, muchas de ellas identificables con técnicas de imagen complementarias, como el ecocardiograma. Debido a que la mayoría de los pacientes se diagnostican como hallazgo casual, están asintomáticos o estables, o tienen bajo riesgo de rotura, son muy pocos los que precisan de tratamiento quirúrgico


Aneurysm dilation of pulmonary artery is a very rare disease and the clinic is non-specific. Final diagnosis relies on imaging tests as computed tomography and nuclear magnetic resonance. They can be idiopathic (less frequent, when an indeterminate etiology occurs) or secondary to several pathologies, most of which can be identified with other imaging tests like echocardiogram. As in most patients the disease is a casual finding, are asymptomatic or with haemodynamic stability or have a low risk of rupture, only a few need surgery


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Aneurisma da Aorta Torácica/diagnóstico , Embolia Pulmonar/diagnóstico , Hipertensão Pulmonar/diagnóstico , Ecocardiografia , Tomografia Computadorizada por Raios X
8.
Arch Esp Urol ; 54(1): 64-6, 2001.
Artigo em Espanhol | MEDLINE | ID: mdl-11296674

RESUMO

OBJECTIVE: To report an uncommon association of prostate and lung cancer. METHODS: The characteristics of both tumors, their association with tumors in other sites and the time of presentation are analyzed. RESULTS: Both tumors were in the advanced stages. Metastatic carcinoma of the prostate was discarded due to the form of presentation. CONCLUSIONS: Although the association of prostate and lung cancer is uncommon, the possibility of synchronous tumors should be considered in patients with urinary and pulmonary symptoms suggestive of neoplasm. It is important to determine if the lesion is a metastasis, since the prognosis depends on the second tumor.


Assuntos
Adenocarcinoma/diagnóstico , Neoplasias Pulmonares/diagnóstico , Neoplasias Primárias Múltiplas/diagnóstico , Derrame Pleural Maligno/etiologia , Neoplasias da Próstata/diagnóstico , Idoso , Humanos , Masculino
9.
Arch Esp Urol ; 53(7): 636-8, 2000 Sep.
Artigo em Espanhol | MEDLINE | ID: mdl-11037659

RESUMO

OBJECTIVE: To describe a case of a solitary pulmonary nodule in a patient that had been treated for carcinoma of the renal pelvis. METHODS: A solitary pulmonary nodule was detected on the chest film of a patient that had been treated for carcinoma of the renal pelvis. The characteristics of the nodule are described and its diagnosis, with special reference to metastasis and primary pulmonary carcinoma, is discussed. RESULTS: The anatomopathological study demonstrated a chondroid hamartoma. CONCLUSIONS: A metastatic or a primary tumor is suspected when a solitary pulmonary nodule is detected in a patient that has been previously treated for urothelial carcinoma. However, other types of lesions with a more favourable outcome cannot be discarded, such as chondroid hamartoma as in the case described herein.


Assuntos
Neoplasias Renais/patologia , Neoplasias Pulmonares/secundário , Nódulo Pulmonar Solitário/secundário , Humanos , Neoplasias Renais/terapia , Pelve Renal , Masculino , Pessoa de Meia-Idade , Nódulo Pulmonar Solitário/terapia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA