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1.
Nihon Kokyuki Gakkai Zasshi ; 49(9): 623-8, 2011 Sep.
Artículo en Japonés | MEDLINE | ID: mdl-22073605

RESUMEN

We reviewed the clinicopathological characteristics of lung abscesses retrospectively. We analyzed 89 patients hospitalized from July 1984 to May 2009. Most were men (76/89). There were large proportions with alcohol consumption (29.2%) and dental caries or gingivitis (60.7%). Furthermore, those without other diseases accounted for only 13.5%. Predominant infectious species were clear in 43 cases (48.3%) including identification of bacteria. The identification rate of predominant bacteria improved from 38.5% to 56.0% after initiation of the introduction of expectoration culture, bronchoscopic specimen collection and gingival culture in 2003, facilitating clarification of the predominant bacteria. The Streptococcus anginosus group with predominant bacteria being slightly aerobic streptococci, anaerobic bacterium, and aerobic bacterium was detected in 10, 12, and 31 cases, respectively. The improvement in the identification rate of predominant bacteria was achieved by carrying out examination with close liaison with the staff of our inspection room. In selecting antimicrobials based on diagnostic significance, we should focus on positive identification of predominant bacteria, a factor which appears to have major clinical significance.


Asunto(s)
Absceso Pulmonar/microbiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Bacterias Aerobias/aislamiento & purificación , Comorbilidad , Femenino , Humanos , Absceso Pulmonar/complicaciones , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Streptococcus anginosus/aislamiento & purificación
2.
Lymphat Res Biol ; 4(3): 143-52, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-17034294

RESUMEN

BACKGROUND: Lymphangioleiomyomatosis (LAM) is a rare destructive lung disease characterized by an abnormal proliferation of smooth muscle-like cells (LAM cells) in the lung and along the axial lymphatics. LAM demonstrates a heterogeneous clinical course, but there is no serum surrogate marker available for assessing the disease severity or predicting the disease progression. Since the authors have recently demonstrated the extensive LAM-associated lymphangiogenesis and its potential role in progression and metastasis of LAM cells, they hypothesized that serum levels of lymphangiogenic growth factors might be increased in LAM and become a surrogate marker for disease severity. METHODS AND RESULTS: VEGF-A, VEGF-C, and VEGF-D in serum of 44 patients with LAM were measured by enzyme-linked immunosorbant assay. Only VEGF-D was significantly increased in LAM patients as compared with age- and gender-matched healthy volunteers (n=24) (LAM vs. control, geometric mean 95% CI; 1069.3 pg/mL (809.4 approximately 1412.6) vs. 295.9 pg/mL (262.6 approximately 333.5), p<0.0001). Serum VEGF-D levels negatively correlated with variables of pulmonary function tests, FEV1/FVC (forced expiratory volume in one second/forced vital capacity) (r=-0.365, p<0.05) and %DLco/VA (the percentage of diffusing capacity for carbon monoxide/alveolar volume to the predicted value) (r=-0.560, p<0.001). As expected, the group who received hormone therapy showed more deteriorated pulmonary function with higher serum VEGF-D levels than the group who was just observed without hormone therapy. Immunohistochemical examination of lung specimens demonstrated the positive immunoreactivity of LAM cells for VEGF-D. CONCLUSION: Serum VEGF-D levels may be a valuable surrogate marker for evaluating the disease severity in LAM.


Asunto(s)
Linfangioleiomiomatosis/sangre , Factor D de Crecimiento Endotelial Vascular/sangre , Adulto , Femenino , Volumen Espiratorio Forzado/efectos de los fármacos , Volumen Espiratorio Forzado/fisiología , Hormonas/farmacología , Hormonas/uso terapéutico , Humanos , Leiomioma/metabolismo , Linfangioleiomiomatosis/tratamiento farmacológico , Linfangioleiomiomatosis/fisiopatología , Persona de Mediana Edad , Miocitos del Músculo Liso/metabolismo , Pruebas de Función Respiratoria , Neoplasias Uterinas/metabolismo , Factor A de Crecimiento Endotelial Vascular/sangre , Factor C de Crecimiento Endotelial Vascular/sangre , Factor D de Crecimiento Endotelial Vascular/metabolismo , Capacidad Vital/efectos de los fármacos , Capacidad Vital/fisiología
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