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1.
Ann Thorac Surg ; 79(1): 254-7; discussion 254-7, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15620952

ABSTRACT

BACKGROUND: In patients undergoing lung resection for non-small cell lung cancer (NSCLC), the primary TNM (tumor-regional lymph node-distant metastasis) staging system is the best prognostic factor. However, it is necessary to investigate other factors that could more accurately predict a patient's prognosis. In this study we evaluated the significance of positive intraoperative pre-resectional lavage in patients with NSCLC. METHODS: We enrolled 84 patients (79 men, 5 women) aged between 36 and 81 years (mean age, 64.8 years) undergoing a major lung resection for NSCLC, with no preoperative evidence of pleural effusions. Intraoperatively, the patients were given a pre-resectional pleural lavage with physiologic saline solution. The fluid was aspirated and sent to cytology. RESULTS: Pre-resectional pleural lavage was positive in 19 patients (22.6%). The lavage was positive in 7.3% in patients with early stage I disease (3/41) and 37.2% in patients with stage II/III disease. In the group of 16 patients with chest wall neoplastic involvement (T3), 9 had a positive lavage (56.2%; p = 0.05). No significant correlation was found between positive lavage and nodal status, visceral pleural involvement, or histologic findings. Patients with malignant cells in the pre-resectional lavage had a significantly shorter survival than patients with a negative lavage (p = 0.025). CONCLUSIONS: A positive cytology finding of intraoperative pre-resectional pleural lavage could be an important prognostic factor in patients undergoing major lung resection for NSCLC. Patients with a positive lavage should be upstaged. However, larger series are needed to define accurately the role of this technique in early stage lung cancer.


Subject(s)
Carcinoma, Non-Small-Cell Lung/pathology , Intraoperative Care/methods , Lung Neoplasms/pathology , Pleural Cavity/cytology , Pleural Effusion, Malignant/diagnosis , Therapeutic Irrigation , Adenocarcinoma/pathology , Adenocarcinoma/secondary , Adenocarcinoma/surgery , Adult , Aged , Aged, 80 and over , Carcinoma, Non-Small-Cell Lung/mortality , Carcinoma, Non-Small-Cell Lung/surgery , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/secondary , Carcinoma, Squamous Cell/surgery , Female , Follow-Up Studies , Humans , Life Tables , Lung Neoplasms/mortality , Lung Neoplasms/surgery , Male , Middle Aged , Neoplasm Invasiveness , Neoplasm Staging , Pleural Effusion, Malignant/pathology , Pneumonectomy , Predictive Value of Tests , Prognosis , Survival Analysis
2.
J Leukoc Biol ; 73(6): 739-46, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12773506

ABSTRACT

In the present study, by comparing the responses in wild-type (WT) mice and mice lacking [knockout (KO)] the 5-lipoxygenase (5-LO), we investigated the role played by 5-LO in the development of acute inflammation. When compared with carragenan-treated 5-LOWT mice, 5-LOKO mice, which had received carrageenan, exhibited a reduced degree of pleural exudation, polymorphonuclear cell migration. Lung myeloperoxidase activity, an index of neutrophil infiltration, was significantly reduced in 5-LOKO mice in comparison with 5-LOWT. Lung-tissue sections from carrageenan-treated 5-LOWT mice showed positive staining for intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), P-selectin, and E-selectin, which were mainly localized around vessels. The intensity and degree of ICAM-1, VCAM-1, P-selectin, and E-selectin were markedly reduced in tissue section from carrageenan-5-LOKO mice, which also improved the histological status of the inflamed lungs. Taken together, our results clearly demonstrate that 5-LO modulates neutrophil infiltration in the acute lung inflammation.


Subject(s)
Arachidonate 5-Lipoxygenase/physiology , Pleurisy/etiology , Pneumonia/etiology , Animals , Arachidonate 5-Lipoxygenase/genetics , Carrageenan , Cell Adhesion Molecules/analysis , Cell Adhesion Molecules/immunology , Cell Adhesion Molecules/metabolism , Immunohistochemistry , Mice , Mice, Knockout , Neutrophil Infiltration , Nitric Oxide/biosynthesis , Pleurisy/chemically induced , Pleurisy/metabolism , Pleurisy/pathology , Pneumonia/chemically induced , Pneumonia/metabolism , Pneumonia/pathology
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