1.Unusual Presentation of Thymic Carcinoma: Hypertrophic Osteoarthropathy.
Seok Jin KIM ; Jae Hong SEO ; Chul Won CHOI ; Eung Seok LEE ; Bo Kyoung SEO ; Jun Suk KIM
The Korean Journal of Internal Medicine 2003;18(2):125-128
Hypertrophic osteoarthropathy is characterized by clubbing and periosteal new bone formation along the shaft of the long bones of the extremities. Although various intrathoracic malignancies have been associated with the development of HOA, it has been extremely rare for HOA to occur in a patient with a thymic carcinoma. Recently, we experienced a 63-year-old woman diagnosed as a thymic carcinoma with hypertrophic osteoarthropathy. She had both digital clubbing and cortical thickening in her lower extremities identified radiologically. We herein describe this case with a review of the literature.
Carcinoma/complications/*diagnosis
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Female
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Human
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Middle Aged
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Osteoarthropathy, Secondary Hypertrophic/*etiology
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Thymus Neoplasms/complications/*diagnosis
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