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Differentiation of jaundice in infancy: An application of radionuclide biliary studies

✍ Scribed by Gerald S. Johnston; Richard C. Rosenbaum; J. Laurance Hill; John N. Diaconis


Book ID
102436527
Publisher
John Wiley and Sons
Year
1985
Tongue
English
Weight
321 KB
Volume
30
Category
Article
ISSN
0022-4790

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✦ Synopsis


Atresia and hypoplasia of the bile ducts are the most common congenital biliary anomalies of clinical importance. Surgical correction can help about 10% of these infants. However, surgery should be performed within the first month of life to avoid irreversible liver parenchymal changes. It is difficult to separate the surgical condition, biliary atresia, from conditions in which the trauma of laparotomy should be avoided, such as neonatal hepatitis and other clinically indistinguishable causes of obstructive jaundice. Radionuclide imaging with the 99mTc-labeled N-substituted iminodiacetic acids (HIDA, PIDIDA, DISIDA, etc) have been helpful in the differential diagnosis of biliary atresia.


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