1.Radiological evaluation of recurrent pyogenic cholangitis
Joo Nam BYON ; Doo Young CHUNG ; Chee Jang SUH ; Jong Jin WON
Journal of the Korean Radiological Society 1984;20(3):615-622
Recurrent pyogenic cholangitis (RPC) is defined as a condition in which there is a primary bacterial cholangitis, characterized clinically by recurrent attacks of fever, chills, abdominal pain, and jaundice. 17 cases of recurrent pyogenic cholangitis at Won Kwang University Hospital during the past three years were analyzedby clinical, radiological and surgical findings. The results were as follows; 1. Peak incidence was noted at fifth decade (35%) and the raio of male to female was almost eual (1:1.1). 2. Most of patients were undernurished andrural population in low socio-economic state. 3. The characteristic and most frequent symptoms were fever, chills,abdominal pain, and jaundice. 4. Serum alkaline phosphatase level was elevated almost 4 times to the upper limitof normal. 5. There was a history of cholecystectomy with or without T-tube drainage in 65% of 17 cases. 6. The cholangiographic findings in the biliary trees were stricture, stones and dilated ducts, and occured more commonly in the left hepatic duct than right. 7. Most stones of biliary trees were pigment stones, and occasionally muddystones were seen. 8. Most of the organism obtained from bile culture were E. coli, supported an infective etiology.
Abdominal Pain
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Alkaline Phosphatase
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Bile
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Chills
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Cholangitis
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Cholecystectomy
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Constriction, Pathologic
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Drainage
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Female
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Fever
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Hepatic Duct, Common
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Humans
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Incidence
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Jaundice
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Male
;
Trees
2.A study on hypophosphatemic vitamin D resistant rickets in a family
Doo Young CHUNG ; Joo Nam BYON ; Chee Jang SUH ; Jong Jin WON
Journal of the Korean Radiological Society 1984;20(3):582-590
Hypophosphatemic vitamin D resistant rickets is a form of rickets characterized by typical structural deformities and roentgenographic and metabolic changes. It has a strong familial tendency and appear to be genetically transmitted. Authors experienced 7 patients with hypophosphatemic vitamin D resistant rickets which have been manifested through three generation in a family at Won-Kwang University Hospital from Dec.1982 to May1984. Authors studied hypophosphatemic vitamin D resistant rickets clinically, radiologically, biochemically andpathologically, and reported with review of literatures.
Congenital Abnormalities
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Humans
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Rickets
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Rickets, Hypophosphatemic