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1.
Tuberculosis and Respiratory Diseases ; : 268-272, 2007.
Article in Korean | WPRIM | ID: wpr-15836

ABSTRACT

A tuberculous pleural effusion may be a sequel to a primary infection or represent the reactivation of pulmonary tuberculosis. It is believed to result from a rupture of a subpleural caseous focus in the lung into the pleural space. It appears that delayed hypersensitivity plays a large role in the pathogenesis of a tuberculous pleural effusion. We encountered a 52 years old man with pleural effusion that developed several days after a CT guided percutaneous needle biopsy of a solitary pulmonary nodule. He was diagnosed with TB pleurisy. It is believed that his pleural effusion probably developed due to exposure of the parenchymal tuberculous focus into the pleural space during the percutaneous needle biopsy. This case might suggest one of the possible pathogeneses of tuberculous pleural effusion.


Subject(s)
Humans , Middle Aged , Biopsy, Needle , Hypersensitivity, Delayed , Lung , Needles , Pleural Effusion , Pleurisy , Rupture , Solitary Pulmonary Nodule , Tuberculosis, Pulmonary
2.
The Journal of the Korean Society for Transplantation ; : 131-136, 2005.
Article in Korean | WPRIM | ID: wpr-194944

ABSTRACT

PURPOSE: Transforming growth factor (TGF)-beta1 and Hypoxia inducible factor (HIF)-1alpha are renal fibrogenetic cytokines involved with the fibrosis of renal allograft. The aim of this study was to investigate TGF-beta1 and HIF-1alpha in renal allograft patients. METHODS: Between January, 1995 and February, 2005, we performed 72 renal allograft biopsies from 61 recipients. Immunohistochemical studies were performed with a immunoperoxidase technique using the primary antibody, rabbit anti-human TGF-beta1 polyclonal antibody (C-teminus, 1:1,000, Santa-Cruz Biotechnology, Santa Cruz, CA, USA) and mouse anti-human HIF-1alpha monoclonal antibody (clone H1alpha 67-sup, 1:1,000, Novus Biological Inc., Littleton, CO, USA). RESULTS: Tubular and interstitial TGF-beta1 expressions in CAN were higher than other groups, showing significant differences (P<0.05). HIF-1alpha expression in CAN was much higher than other groups (P<0.05). The glomerular TGF-beta1 expression of the heavy proteinuria (2.5 gm/day <) group was significantly higher than the low proteinuria group (<1.0 gm/day) (P<0.05). The tubular TGF-beta1 expression of the graft functioning group was significantly lower than the graft loss group (P<0.05). CONCLUSION: In conclusion, HIF-1alpha expression in renal allograft strongly suggests the development of CAN as well as tubular or interstitial TGF-beta1 expression. TGF-beta1 expression in the glomerulus shows significant correlation with the amount of 24 hours urine protein. The tubular TGF-beta1 expression has strong correlation with graft survival.


Subject(s)
Animals , Humans , Mice , Allografts , Hypoxia , Biopsy , Biotechnology , Cytokines , Fibrosis , Graft Survival , Immunoenzyme Techniques , Kidney Transplantation , Proteinuria , Transforming Growth Factor beta1 , Transforming Growth Factors , Transplants
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