1.A Case of Cholecysto-gastro-colonic Fistula with Upper Gastrointestinal Bleeding.
Min Kyu PARK ; Yun Jin CHUNG ; In Yub BAEK ; Hyeong Seok KIM ; Sang Soo BAE ; Su Ok LEE ; Kyoung Suk LEE ; Jong Kyu KWON
The Korean Journal of Gastroenterology 2013;61(5):290-293
Biliary enteric fistula is an abnormal pathway often caused by biliary disease. It is difficult to diagnose the disease because patients have nonspecific symptoms. A 67-year-old woman presented with hematemesis and melena. She was diagnosed with Dieulafoy lesion on the gastric antrum and underwent endoscopic hemostasis using hemoclips. Follow-up upper gastrointestinal endoscopy revealed an abnormal opening on a previous treated site that was suggestive of biliary enteric fistula. Abdomen simple X-ray and abdominal dynamic CT scan showed pneumobilia and cholecysto-gastric fistula. The patient had cholecystectomy and wedge resection of the gastric antrum, followed by right extended hemicolectomy because of severe adhesive lesion between the gallbladder and colon. She was diagnosed with cholecysto-gastro-colic fistula postoperatively. We report on this case and give a brief review of the literatures.
Aged
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Biliary Fistula/complications/*diagnosis/surgery
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Cholecystectomy
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Endoscopy, Gastrointestinal
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Female
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Gastric Fistula/complications/*diagnosis/surgery
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Gastrointestinal Hemorrhage/complications/*diagnosis
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Humans
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Intestinal Fistula/complications/*diagnosis/surgery
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Tomography, X-Ray Computed
2.Improved severe hepatopulmonary syndrome after liver transplantation in an adolescent with end-stage liver disease secondary to biliary atresia.
Tae Jun PARK ; Keun Soo AHN ; Yong Hoon KIM ; Hyungseop KIM ; Ui Jun PARK ; Hyoung Tae KIM ; Won Hyun CHO ; Woo Hyun PARK ; Koo Jeong KANG
Clinical and Molecular Hepatology 2014;20(1):76-80
Hepatopulmonary syndrome (HPS) is a serious complication of end-stage liver disease, which is characterized by hypoxia, intrapulmonary vascular dilatation, and liver cirrhosis. Liver transplantation (LT) is the only curative treatment modality for patients with HPS. However, morbidity and mortality after LT, especially in cases of severe HPS, remain high. This case report describes a patient with typical findings of an extracardiac pulmonary arteriovenous shunt on contrast-enhanced transesophageal echocardiography (TEE), and clubbing fingers, who had complete correction of HPS by deceased donor LT. The patient was a 16-year-old female who was born with biliary atresia and underwent porto-enterostomy on the 55th day after birth. She had been suffered from progressive liver failure with dyspnea, clubbing fingers, and cyanosis. Preoperative arterial blood gas analysis revealed severe hypoxia (arterial O2 tension of 54.5 mmHg and O2 saturation of 84.2%). Contrast-enhanced TEE revealed an extracardiac right-to-left shunt, which suggested an intrapulmonary arteriovenous shunt. The patient recovered successfully after LT, not only with respect to physical parameters but also for pychosocial activity, including school performance, during the 30-month follow-up period.
Adolescent
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Anoxia
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Arteriovenous Fistula/etiology
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Biliary Atresia/*diagnosis/etiology
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Cyanosis/complications
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Dyspnea/complications
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Echocardiography, Transesophageal
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End Stage Liver Disease/complications/*surgery
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Female
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Hepatic Artery/abnormalities
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Hepatopulmonary Syndrome/*diagnosis/ultrasonography
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Humans
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*Liver Transplantation
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Osteoarthropathy, Secondary Hypertrophic/complications