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307 THE DIAGNOSTIC VALUE OF ENDOSCOPIC RETROGRADE QqOLANGIO-PANCREATICOGRAPHY (ERCP) IN PATIENTS WITH ~OLESTATIC SYNDP~ WITHOUT DIIATEDDUCTS. S.H. Yap~ S.P. Strijk x, U.J.G.M. van Haelst xx Div. Of G.I. and liver disease, Dept. of Med., XDept. of diagnostic Radiology and XXDept. of Pathology, St. Radboud Univ. Hospital, Nijmegen, The Netherlands For the diagnosis of a cholestatic syndrome, clinical features and biochemical data are necessary. However, visualization of biliary tree is important for distinguishing between medical and surgical jaundice. For the diagnostic evaluation of cholestatic patients without evidence of dilated ducts on ultrasonogram, a percutaneous liver biopsy has beenusually re- con~nended as the procedure of choice. To determine the values of ERCP and liver biopsy in such patients, 59 patients (28 males, 31 females, 17-79 years) with cholestatic syndrome (alk. phosphatase >2 times of normal value, predominating over the increased levels of serum transaminases) were studied. Most of these patients were jaundiced or complained of itching. The, findings of these two methods of investigations were concordant in 38 patients, while a non-concordant finding was found in 11 patients (4 patients with normal ERCP and extrahepati¢ cholestasis on histology, 2 patients with normal histology and duct 5tenosis, 5 patients with hepatocellular abnormalities (steatosis, PBC, chr. hepatitis) and duct stenosis). The final clinical diagnosis was obtained in all but 13 patients. Conclusion: ERCP is an useful diagnostic aid in cholestasis also in patients with non-dilated ducts on ultrasonogram. A percutaneous liver biopsy is only indicated in such patients when the ERCP failed to demonstrate biliary abnormalities. In case of extrahepatic cholestasis diagnosed by a liver biopsy, ERCP is still necessary to facilitates the management of patien~ with biliary and/or pancreatic disease. 308 ACTIVATED T LYMPHOCYTES IN CHILDREN WITH CHRONIC ACTIVE HEPATITIS (CAH) A.Yeo, L.Alvlggi,D.Vergani,G.Mieli-Vergani, A.P.Mowat Depts of Child Health and Immunology*, King's College Hospital, London. Ia-antigen is detected on T-lymphocytes when the are actively involved in immune- reactions, e.g. viral disease (mononucleoSis) and immune-mediated disorders (rheumatoid arthritis, Grave's disease, Juvenile diabetes, SLE). To investigate whether activation of T-lymphocytes plays a role in the immune-mechanisms leading to CAH we have determined numbers of Ia +re T-cells in 11 samples from 9 children with CAH. Controls were 15 age- matched healthy children and 14 children with other chronic liver diseases. T-lymphoeytes were purified by E-rosetting and Ia+ve T-cells were detected by direct immunofluorescence with anti-Ia monoclonal antibody. Numbers of Ia+ve T-cells were significantly higher in patients with uncontrolled CAH (mean 8.2 SD 1.8) when compared to healthy controls (2.8 - 1; p < 0.01, Hank test) and to other chronic liver diseases (3.5+- 0.9 ; p(O.O1, Rank test) but were normal in 6 treated patients with inactive disease (.2.9 ~ 1.3). Two patients with high numbers of Ia+ve T-cells at diagnosis showed normal values when retested during immuno- suppressive treatment. Increased numbers of Ia+ve T-cells in CAH, but not in other chronic liver diseases, and their return to normal during effective treatment, suggest the participation of activated T-lymphocytes in the immune-mechanisms leading to liver damage in CAN. S154

The diagnostic value of endoscopic retrograde cholangio-pancreaticography (ERCP) in patients with cholestatic syndrome without dilated ducts

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307 THE DIAGNOSTIC VALUE OF ENDOSCOPIC RETROGRADE QqOLANGIO-PANCREATICOGRAPHY (ERCP) IN PATIENTS WITH ~OLESTATIC SYNDP~ WITHOUT DIIATEDDUCTS.

S.H. Yap~ S.P. Strijk x, U.J.G.M. van Haelst xx Div. Of G.I. and liver disease, Dept. of Med., XDept. of diagnostic Radiology

and XXDept. of Pathology, St. Radboud Univ. Hospital, Nijmegen, The Netherlands

For the diagnosis of a cholestatic syndrome, clinical features and biochemical data are necessary. However, visualization of biliary tree is important for distinguishing between medical and surgical jaundice. For the diagnostic evaluation of cholestatic patients without evidence of dilated ducts on ultrasonogram, a percutaneous liver biopsy has beenusually re- con~nended as the procedure of choice. To determine the values of ERCP and liver biopsy in such patients, 59 patients (28 males, 31 females, 17-79 years) with cholestatic syndrome (alk. phosphatase >2 times of normal value, predominating over the increased levels of serum transaminases) were studied. Most of these patients were jaundiced or complained of itching. The, findings of these two methods of investigations were concordant in 38 patients, while a non-concordant finding was found in 11 patients (4 patients with normal ERCP and extrahepati¢ cholestasis on histology, 2 patients with normal histology and duct 5tenosis, 5 patients with hepatocellular abnormalities (steatosis, PBC, chr. hepatitis) and duct stenosis). The final clinical diagnosis was obtained in all but 13 patients. Conclusion: ERCP is an useful diagnostic aid in cholestasis also in patients with non-dilated ducts on ultrasonogram. A percutaneous liver biopsy is only indicated in such patients when the ERCP failed to demonstrate biliary abnormalities. In case of extrahepatic cholestasis diagnosed by a liver biopsy, ERCP is still necessary to facilitates the management of patien~ with biliary and/or pancreatic disease.

308 ACTIVATED T LYMPHOCYTES IN CHILDREN WITH CHRONIC ACTIVE HEPATITIS (CAH)

A.Yeo, L.Alvlggi,D.Vergani,G.Mieli-Vergani, A.P.Mowat

Depts of Child Health and Immunology*, King's College Hospital, London.

I a - a n t i g e n i s d e t e c t e d o n T - l y m p h o c y t e s w h e n t h e a r e a c t i v e l y i n v o l v e d i n i m m u n e - r e a c t i o n s , e . g . v i r a l d i s e a s e ( m o n o n u c l e o S i s ) a n d i m m u n e - m e d i a t e d d i s o r d e r s ( r h e u m a t o i d a r t h r i t i s , G r a v e ' s d i s e a s e , J u v e n i l e d i a b e t e s , S L E ) . To i n v e s t i g a t e w h e t h e r a c t i v a t i o n o f

T - l y m p h o c y t e s p l a y s a r o l e i n t h e i m m u n e - m e c h a n i s m s l e a d i n g t o CAH we h a v e d e t e r m i n e d n u m b e r s o f I a + r e T - c e l l s i n 11 s a m p l e s f r o m 9 c h i l d r e n w i t h CAH. C o n t r o l s w e r e 1 5 a g e - m a t c h e d h e a l t h y c h i l d r e n a n d 14 c h i l d r e n w i t h o t h e r c h r o n i c l i v e r d i s e a s e s . T - l y m p h o e y t e s w e r e p u r i f i e d b y E - r o s e t t i n g a n d I a + v e T - c e l l s w e r e d e t e c t e d b y d i r e c t i m m u n o f l u o r e s c e n c e w i t h a n t i - I a m o n o c l o n a l a n t i b o d y . N u m b e r s o f I a + v e T - c e l l s w e r e s i g n i f i c a n t l y h i g h e r i n p a t i e n t s w i t h u n c o n t r o l l e d CAH ( m e a n 8 . 2 SD 1 . 8 ) w h e n c o m p a r e d t o h e a l t h y c o n t r o l s ( 2 . 8 - 1 ; p < 0 . 0 1 , H a n k t e s t ) a n d t o o t h e r c h r o n i c l i v e r d i s e a s e s (3 .5+- 0 . 9 ; p ( O . O 1 , R a n k t e s t ) b u t w e r e n o r m a l i n 6 t r e a t e d p a t i e n t s w i t h i n a c t i v e d i s e a s e ( . 2 . 9 ~ 1 . 3 ) . Two p a t i e n t s w i t h h i g h n u m b e r s o f I a + v e T - c e l l s a t d i a g n o s i s s h o w e d n o r m a l v a l u e s w h e n r e t e s t e d d u r i n g i m m u n o - s u p p r e s s i v e t r e a t m e n t . I n c r e a s e d n u m b e r s o f I a + v e T - c e l l s i n CAH, b u t n o t i n o t h e r c h r o n i c l i v e r d i s e a s e s , a n d t h e i r r e t u r n t o n o r m a l d u r i n g e f f e c t i v e t r e a t m e n t , s u g g e s t t h e p a r t i c i p a t i o n o f a c t i v a t e d T - l y m p h o c y t e s i n t h e i m m u n e - m e c h a n i s m s l e a d i n g t o l i v e r d a m a g e i n CAN.

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