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신장 이식 환자에서 통상적인 용량의 비스무트 포함 약제 복용 후 발생한 피부 과다색소침착 1예
최우석 ( Woo Suk Choi ),최하늘 ( Han Ul Choi ),정지용 ( Ji Yong Jung ),장제현 ( Jae Hyun Chang ),정우경 ( Woo Kyung Chung ),이현희 ( Hyun Hee Lee ) 대한신장학회 2011 Kidney Research and Clinical Practice Vol.30 No.6
A 59-year-old male presented with multiple hyperpigmented skin with hyperkeratotic scaly patches on hands, feet and face. Bismuth containing compound had been prescribed two months before then due to epigastric pain, an adverse effect of steroid pulse therapy for acute rejection of transplanted kidney. Laboratory findings showed acute kidney injury and elevated liver enzyme. He stopped taking bismuth containing compound and all symptoms were gone after two months. Although there is no report on interaction between bismuth and immunosuppressant, it requires precaution to prescribe bismuth containing compounds in transplanted patients with acute kidney injury.
진기남,정우경,장승연,Jin, Ki-Nam,Chung, Woo-Kyung,Jang, Seung-Yon 대한예방의학회 1997 예방의학회지 Vol.30 No.2
The purpose of this study is to examine the factors influencing the allergic rhinitis patients' satisfaction with laser surgery. The data were collected by telephone interviews with 211 patients who visited I university hospital. The statistical methods used for the analysis were factor analysis, reliability test, and hierarchical multiple regression. We find that satisfaction level is a function of not only the surgery outcome but also the socio-psychological experience during treatment. With the improvement in nasal allergic condition, patients were more likely to be satisfied with medical services. And patients who had positive experience with physicians and facilities reported higher satisfaction level. While the surgery outcome explained 68% of the variation of satisfaction level, socio-psychological experience explained 23% of it. This result clearly shows that physicians need to pay attention to the socio-psychological aspect as well as the technical aspect of medical services.
결절성경화증 환자에서 신장과 간 혈관근지방종 및 폐 침범 2예
이현희 ( Hyun Hee Lee ),정우경 ( Woo Kyung Chung ),장제현 ( Jae Hyun Chang ),정지용 ( Ji Young Jung ),성지윤 ( Ji Yoon Sung ),나선영 ( Sun Young Na ),성연미 ( Yon Mi Sung ) 대한내과학회 2010 대한내과학회지 Vol.79 No.6
Tuberous sclerosis (TS) involves multiple organs. Angiomyolipoma of the liver or kidney is one of the clinical manifestations of TS. However, coexistent renal and hepatic angiomyolipoma associated with TS is a rare condition. Pulmonary involvement is extremely rare, and occurs in only 0.1~1% of TS. We report two cases of concurrent renal and hepatic angiomyolipomas with pulmonary involvement in patients with TS. The first case was a 35 year-old woman who showed multiple angiomyolipomas in the liver and both kidneys and cystic parenchymal changes in the lungs. The other case was a 27-year-old woman who showed multiple angiomyolipomas in the liver and both kidneys, and multinodular pulmonary shadows. To the best of our knowledge, this is the first reported case of renal and hepatic angiomyolipomas associated with pulmonary involvement in Korea. (Korean J Med 79:705-709, 2010)
박철희 ( Cheul Hee Park ),정낙소 ( Nak So Chung ),정우경 ( Woo Kyung Chung ),방수미 ( Soo Mee Bang ),이종호 ( Jong Ho Lee ),정재걸 ( Jae Gul Chung ),이준승 ( Joon Seung Lee ) 대한내과학회 2005 대한내과학회지 Vol.69 No.-
There are only a few reports of glomerulonephritis associated with polycythemia vera (PV). These cases include diffuse mesangial proliferative glomerulonephritis (mesPGN), Henoch-Schonlein purpura nephritis, focal segmental glomerulonephritis and IgA nephropathy. In 1983, Plomley et al. reported on 3 cases of mesPGN in patients with PV for the first time. However the possibility that these cases were IgA nephropathy could not be excluded since there was no data of electron microscopic or immnunofluorescent (IF) study. We report a case of idiopathic mesPGN combined with PV. A 46-year-old male was referred to our hospital because of proteinuria and splenomegaly on his routine medical examination. While undergoing investigation for the proteinuria, the patient was found to have a high hemoglobin (22.3 g/dL) and hematocrit (68.8%) levels. At that time, the urinary protein excretion was 3.0 g in 24 hour. We diagnosed the patient as a case of PV by World Health Organization criteria. The renal biopsy revealed focal mesangial proliferation with expansion of the matrix. On IF study, there was no deposition of IgA, IgG and C3 in the mesangium. (Korean J Med 69:S884-S889, 2005)
급성 포르피리아 발작중 발생한 심한 저나트륨혈증 1 예
정철원(Chul Won Jung),전은실(Un Sil Jeon),정우경(Woo Kyung Chung),김원석(Won Seog Kim),조종태(Jong Tai Cho),안규리(Cu Rie Ahn),한진석(Jin Suk Han),김성권(Suhng Gwon Kim),이정상(Jung Sang Lee) 대한내과학회 1995 대한내과학회지 Vol.49 No.2
Hepatic porphyria shows impaired heme biosynthesis predominantly in the liver and usually presents with abdominal pain, vomiting, photosensitivity and neurologic abnormalities and sometimes with hyponatremia accompanied by syndrome of inappropriate antidiuretic hormone secretion(SIADH). We report a case seemed to be a hereditary coproporphyria presenting with acute abdominal pain and vomiting. She had severe hyponatremia with the feature of SIADH and peripheral neuropathy which was provoked by the ingestion of alcohol, poor oral intake and by the administration of imipramine. She was thought to have hereditary coproporphyria by the clinical feature, stool porphyrin and quantitation of the 24 hour urine δ-aminolevulinic acid, porpho-bilinogen and porphyrins. Supportive treatment with NaCI infusion and propranolol resulted in symptomatic recovery and she was discharged after education of precipitating factors.