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1.
Ann Thorac Surg ; 60(3): 710-2, 1995 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-7677514

RESUMEN

Fibrous histiocytomas are uncommon pulmonary tumors. They generally involve only the lung parenchyma. Endobronchial involvement is extremely rare. Usually, surgical resection of the mass is required for definitive diagnosis and therapy. We report a case of benign atypical fibrous histiocytoma visualized during fiberoptic bronchoscopy and review the clinical findings and pathologic features of this tumor.


Asunto(s)
Neoplasias de los Bronquios/patología , Histiocitoma Fibroso Benigno/patología , Adulto , Obstrucción de las Vías Aéreas/patología , Obstrucción de las Vías Aéreas/cirugía , Neoplasias de los Bronquios/cirugía , Broncoscopía , Femenino , Tecnología de Fibra Óptica , Histiocitoma Fibroso Benigno/cirugía , Humanos , Neumonectomía
3.
Chest ; 102(6): 1672-5, 1992 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-1446470

RESUMEN

Random assessments of SaO2 were performed via pulse oximetry in 274 hospitalized non-ICU patients prescribed supplemental O2 in a large tertiary care university hospital. In 507 assessments performed in patients inspiring the prescribed O2, 426 were receiving excessive amounts of O2 to maintain a SaO2 > or = 92 percent. In 233 of these assessments, SaO2 was > or = 92 percent while breathing ambient air. In an additional 193 assessments, the concentration of inspired supplemental O2 was excessive to maintain a SaO2 > or = 92 percent. However, in 81 assessments performed in patients inspiring O2, the prescribed amount was insufficient to maintain SaO2 > or = 92 percent. These results indicate that O2 prescription in hospitalized non-ICU patients is excessive or not required in the majority of cases. Furthermore, routine use of pulse oximetry in hospitalized patients prescribed O2 may be useful in determining the continued need for supplemental O2 and adjusting the proper concentration needed to avoid hypoxemia.


Asunto(s)
Hospitales Universitarios/estadística & datos numéricos , Terapia por Inhalación de Oxígeno/estadística & datos numéricos , Baltimore/epidemiología , Protocolos Clínicos , Control de Costos , Ahorro de Costo , Costos y Análisis de Costo , Hospitales Universitarios/economía , Humanos , Reembolso de Seguro de Salud , Unidades de Cuidados Intensivos , Oximetría , Oxígeno/sangre , Terapia por Inhalación de Oxígeno/economía , Cooperación del Paciente , Mecanismo de Reembolso , Servicio de Terapia Respiratoria en Hospital/economía , Servicio de Terapia Respiratoria en Hospital/estadística & datos numéricos , Factores de Tiempo , Recursos Humanos
4.
Am J Med ; 87(6): 664-8, 1989 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-2686434

RESUMEN

A variety of pulmonary complications related to the use of freebase cocaine have been reported in the medical literature. Pulmonary barotrauma, hypersensitivity pneumonitis, pulmonary hemorrhage, obliterative bronchiolitis, asthma, and pulmonary edema have all recently been described. The number of reports are few, reflecting either the low incidence of these complications or the lack of recognition of these phenomena as cocaine-related illnesses. The mechanism by which freebase cocaine can injure the lung is not well defined. Whether an abnormal immunologic response to cocaine freebase can result in hemorrhage, pneumonitis, bronchiolitis, or asthma remains speculative. Whether cardiogenic or non-cardiogenic factors play a role in the development of pulmonary edema in freebase smokers has not yet been determined. Likewise, the roles of either cocaine, tobacco, or adulterants in producing the observed abnormalities of lung function remain controversial. Further reporting of freebase-related pulmonary complications, as well as the development of appropriate animal models, is needed.


Asunto(s)
Cocaína/farmacología , Enfermedades Pulmonares/inducido químicamente , Trastornos Relacionados con Sustancias , Administración por Inhalación , Barotrauma/inducido químicamente , Bronquiolitis Obliterante/inducido químicamente , Hemorragia/inducido químicamente , Humanos , Alveolos Pulmonares/lesiones , Edema Pulmonar/inducido químicamente , Hipersensibilidad Respiratoria/inducido químicamente
5.
Chest ; 96(5): 1050-3, 1989 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-2805835

RESUMEN

A reduction in the DCO has been reported among "free-base" cocaine smokers. We reviewed the pulmonary histopathology in 20 deaths due to cocaine intoxication for either parenchymal or vascular abnormalities which might explain this physiologic finding. Pulmonary artery medical hypertrophy in the absence of foreign particle microembolization was present in four of 20 cases (20 percent). Hemosiderin-laden macrophages were found in seven of 20 cases (35 percent). These abnormalities were not seen in a matched control group. We conclude that in the absence of foreign particle microembolization, pulmonary artery medial hypertrophy occurs among cocaine users, although the mechanism of these vascular changes is unknown. In addition, occult alveolar hemorrhage occurs more frequently among cocaine users than is clinically recognized.


Asunto(s)
Cocaína , Cuerpos Extraños , Pulmón , Arteria Pulmonar/patología , Trastornos Relacionados con Sustancias/patología , Adulto , Cocaína/envenenamiento , Femenino , Humanos , Hipertrofia , Pulmón/patología , Masculino , Arteria Pulmonar/efectos de los fármacos , Circulación Pulmonar/efectos de los fármacos , Capacidad de Difusión Pulmonar/efectos de los fármacos , Embolia Pulmonar
6.
Clin Nucl Med ; 14(5): 341-3, 1989 May.
Artículo en Inglés | MEDLINE | ID: mdl-2656040

RESUMEN

Hepatic hydrothorax is a complication in approximately 5% of patients with cirrhosis. Ascites is almost always present and helps to suggest the correct diagnosis. However, when ascites is absent, radionuclide imaging has proven to be helpful in establishing that the pleural effusion originated from ascitic fluid. When pleural fluid is rapidly removed, such as by thoracostomy tube drainage, the radioisotope may accumulate outside the thorax and produce a negative scan of the chest. When the radionuclide scan is nondiagnostic and the pleural space is being rapidly drained, the pleural fluid collecting system should always be imaged before rejecting a diagnosis of hepatic hydrothorax.


Asunto(s)
Drenaje , Hidrotórax/diagnóstico por imagen , Cirrosis Hepática/complicaciones , Toracostomía , Femenino , Humanos , Hidrotórax/etiología , Hidrotórax/cirugía , Persona de Mediana Edad , Compuestos Organometálicos , Ácido Pentético , Cintigrafía , Tecnecio , Pentetato de Tecnecio Tc 99m
7.
J Immunol ; 141(12): 4306-12, 1988 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-2848893

RESUMEN

Collagenase catalyzes the initial and rate-limiting step in interstitial collagen degradation. Human alveolar macrophages produce both a fibroblast-like procollagenase and tissue inhibitor of metalloproteinases (TIMP). To define the potential of macrophages to express collagenase and TIMP, we have studied the effects of certain cell culture variables and LPS on in vitro production of these proteins. Our data indicate: 1) human macrophages cultured in a 1/1 (v/v) mixture of HAM F-12:DME produce two- to three-fold greater quantities of procollagenase (but not TIMP) as compared to HAM F-12, DME, or alpha-MEM alone; 2) maximal collagenase expression requires the further addition of LPS, whereas TIMP production is optimized by 5% fetal bovine serum alone; 3) the up-regulation of macrophage procollagenase by LPS represents a highly selective biologic response when compared to changes induced in other secreted and intracellular proteins; 4) measurements of steady state procollagenase mRNA by Northern blot analysis suggest that the LPS effect is mediated at a pre-translational level; and finally 5) on a per cell basis, human alveolar macrophages cultured under optional conditions secrete approximately 20% of the collagenase and approximately 10% of the TIMP elaborated by stimulated human fibroblasts. We conclude that procollagenase and TIMP secretion by human alveolar macrophages in vitro is strikingly responsive to variations in cell culture conditions and that an especially noteworthy selective upregulation of procollagenase secretion by LPS is probably modulated by a transcriptional mechanism. The macrophage synthetic potential for procollagenase suggests a potentially important role for these cells in directly mediating collagen turnover.


Asunto(s)
Colagenasas , Fibroblastos/enzimología , Lipopolisacáridos , Macrófagos/enzimología , Colagenasa Microbiana/biosíntesis , Alveolos Pulmonares , Adulto , Células Cultivadas , Medios de Cultivo , Inhibidores Enzimáticos/inmunología , Inhibidores Enzimáticos/metabolismo , Precursores Enzimáticos/biosíntesis , Precursores Enzimáticos/metabolismo , Sangre Fetal , Fibroblastos/efectos de los fármacos , Humanos , Macrófagos/efectos de los fármacos , Colagenasa Microbiana/antagonistas & inhibidores , Colagenasa Microbiana/inmunología , Colagenasa Microbiana/metabolismo , Biosíntesis de Proteínas , Inhibidores Tisulares de Metaloproteinasas
8.
Chest ; 94(1): 193-5, 1988 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-3383632

RESUMEN

Interstitial pneumonitis in sarcoidosis is rare. When present, it confined to areas of active granuloma formation. We report finding widespread interstitial pneumonitis and fibrosis in a patient with sarcoidosis. Due to the focal sampling of pulmonary tissue by transbronchial biopsy, a finding of interstitial pneumonitis does not exclude a diagnosis of sarcoidosis.


Asunto(s)
Enfermedades Pulmonares/patología , Pulmón/patología , Fibrosis Pulmonar/patología , Sarcoidosis/patología , Adulto , Biopsia , Femenino , Humanos
9.
Chest ; 93(2): 427-9, 1988 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-3338316

RESUMEN

Previous reports of respiratory complications from cocaine abuse have focused on pulmonary barotrauma or a reduction in carbon monoxide diffusing capacity. We report a patient who developed life-threatening alveolar hemorrhage following repeated inhalation of alkaloid cocaine.


Asunto(s)
Cocaína , Hemorragia/inducido químicamente , Enfermedades Pulmonares/inducido químicamente , Trastornos Relacionados con Sustancias/complicaciones , Adulto , Femenino , Hemorragia/patología , Humanos , Enfermedades Pulmonares/patología , Alveolos Pulmonares/patología
10.
Am Rev Respir Dis ; 135(6): 1281-5, 1987 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-2438967

RESUMEN

Elastase activity directed against lung extracellular matrix is currently believed to be important in the pathogenesis of pulmonary emphysema. Although human alveolar macrophages degrade elastin when in direct contact with this substrate in vitro, studies of free elastase activity in medium conditioned by human alveolar macrophages have yielded variable results. As human alveolar macrophages secrete the tissue inhibitor of metalloproteinases (TIMP), an inhibitor of collagenase and of other connective-tissue-derived mammalian metalloproteinases, we speculated that this inhibitor's effects might extend to macrophage elastase. Using metalloproteinase elastase from the murine macrophagelike cell line P388D1, we observed that human alveolar macrophage conditioned medium inhibits metalloproteinase elastase and that this inhibitory activity could be blocked by specific antibody to TIMP. Alpha 2-macroglobulin, another proteinase inhibitor secreted by alveolar macrophages, also inhibited metalloproteinase elastase, but its inhibitory capacity was not blocked by antibody to TIMP. Because detergents are often included in elastase assays, we examined the effects of sodium dodecyl sulfate (SDS). Buffers containing SDS and SDS-treated elastin were found to exert diverse effects on metalloproteinase elastase, TIMP, and alpha 2-macroglobulin activities, including a marked inhibition of metalloproteinase elastase activity by SDS-containing buffers. These findings suggest that detection of secreted metalloproteinase elastase activity by human alveolar macrophages is complicated by the concomitant release by these cells of inhibitors of metalloproteinases, and that assay conditions can markedly influence the results.


Asunto(s)
Inhibidores Enzimáticos/metabolismo , Macrófagos/metabolismo , Metaloendopeptidasas , Inhibidores de Proteasas , Alveolos Pulmonares/citología , Anticuerpos/inmunología , Endopeptidasas/metabolismo , Inhibidores Enzimáticos/inmunología , Inhibidores Enzimáticos/farmacología , Humanos , Técnicas In Vitro , Metaloproteinasa 12 de la Matriz , Dodecil Sulfato de Sodio/farmacología , Inhibidores Tisulares de Metaloproteinasas , alfa-Macroglobulinas/farmacología
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