Interstitial Pneumonitis in a Patient with Chronic Hepatitis C and Chronic Renal Failure on Interferon Therapy.
	    		
		   		
		   			
		   		
	    	
    	- Author:
	        		
		        		
		        		
			        		Eun Jung KANG
			        		
			        		
			        		
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			        		Dong Kyun KIM
			        		
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			        		Seong Ran JEON
			        		
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			        		Hyun Sook CHOI
			        		
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			        		Soung Won JEONG
			        		
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			        		Jae Young JANG
			        		
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			        		Joon Seong LEE
			        		
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			        		Soo Taek UH
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Case Report
 - Keywords: Chronic hepatitis C; Interferon; Chronic renal failure; Interstitial pneumonitis
 - MeSH: Antiviral Agents/*adverse effects/therapeutic use; Bronchoalveolar Lavage; Female; Hepatitis C, Chronic/complications/*drug therapy; Humans; Interferon-alpha/*adverse effects/therapeutic use; Kidney Failure, Chronic/complications; Lung Diseases, Interstitial/*chemically induced/pathology/radiography; Middle Aged; Respiratory Function Tests; Tomography, X-Ray Computed
 - From:The Korean Journal of Gastroenterology 2011;58(1):47-52
 - CountryRepublic of Korea
 - Language:English
 - Abstract: After 4-months of alpha interferon (IFN-alpha), a 64-year old woman with chronic hepatitis C developed a cough and dyspnea and showed diffuse infiltrative opacities on her chest X-ray. Her symptoms persisted after stopping the IFN-alpha therapy. Pulmonary function testing revealed a reduced forced vital capacity. High-resolution computed tomography of the lung showed peripheral and peribronchovascular ground glass attenuation and consolidation associated with reticulation. Bronchoalveolar lavage was performed for further evaluation and showed a lymphocyte level of 8.2%, an uncommon finding in IFN-alpha-induced interstitial pneumonitis. We performed a lung biopsy to diagnose her disease and it suggested interstitial pneumonitis. This was considered to be due to the immunomodulatory effects of INF-alpha. Although rare, any sign of significant pulmonary involvement should be evaluated.
 
            