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박경득(Kyung Deuk Park),임성빈(Sung Bin Im),한승경(Seung Kyung Hann),박윤기(Yoon Kee Park) 대한피부과학회 1992 대한피부과학회지 Vol.30 No.6
Persistent light reaction is a condition of chronic photodermatitis in which photosensitive reaction persists even after the rernoval of all photosensilizers. A 56-year-old man had experienced a recurrent dermatitis involving primarily the face, neek, forearms and hands for 9 years, this condition was aggravated by sunexposure. Photopatch testing disclosed a strongly positive reaction to chloropromazine, promethazine, acid trichlorocarbanilide, Phototesting also revealed lowered MED with UVA and UVB thar norrmal mean value. (Kor J Dermatd 1992;30(8):901-905)
Methicillin 내성 황색 포도상구균에 의한 다발성 절종증
박경득(Kyung Deuk Park),조남준(Nam Joon Cho),방동식(Dong Sik Bang),김덕현(Duck Hyun Kim) 대한피부과학회 1993 대한피부과학회지 Vol.31 No.1
Staphylococcus aureus is one of many causative agents of the fu uncles. As the S. aureus strains resistant to penicillinase-repsistant penicillins (methicillin-resistant S. aureus, MRSA) are more frequently isolated, their accuiate identification became a very important step in selection of an appropriate therapeutic regimen. We report herein a case of multiple furunculosis caused by metkicillin-resistant S. aureus in a 11-year-old male patient, who was successfully treated with sulbactam/ampicillin and amikacin. (Kor J Dermatol 1993; 31(1): 83-86)
박욱화(Wook Hwa Park),박태현(Tae Hyun Park),박경득(Kyung Deuk Park),방동식(Dong Sik Bang),전수일(Soo Il Chun) 대한피부과학회 1995 대한피부과학회지 Vol.33 No.1
The onset of systemic scleroderma in the first. decade of lif occurs in less than 1.5% of instances. Systemic sclerodrma in childhood have been characterized by less severe visceral involvement and a benign course We report a boy, aged 7 years, with a history of Raynaid; phenomenon and dysphagia. He had a mask-like face, flexion contracture of hands and knee joints, digital pitting scars, ichthyosiform skin change on leg and hyperpigrnented induration on all extremities and trunk. Antinuclear antibodies were positive in nucleolar type and Scl-70 antiocy was also present. On radiologie study, the pattern of reflux esophagitis and resorption of the listal ends of all phalanges were nated. Histopathological findings were compatible with sclerodma. He was treated with Penicillamine-D and oral corticosteroic with good improvernent. (Kor J Dermatol 1995; 33(1): 183-187)
Prednisolone과 Interferon alfa - 2a로 치료하여 호전된 미만성 신생아 혈관종증
조흔정 ( Heun Jung Cho ),김동건 ( Dong Kun Kim ),박경득 ( Kyung Deuk Park ),양창현 ( Chang Hyun Yang ),이진용 ( Jin Yong Lee ),김길영 ( Kir Young Kim ) 대한피부과학회 1996 대한피부과학회지 Vol.34 No.6
Diffuse neonatal hemangiomatosis is a disease often with a fatal out,come, characterized by widespread capillary hemangiomias of the skin and visceral organs. A 6 month old-girl was diagnosed to have diffuse neonatal hemangiomatosis by her multiple hemangiomas on the skin, liver, brain, lung and oral mucosa. She was treated with prednisolone 1.5-2rng/kg/day for 9 months and combined interferon alfa-2a 3 million unit/m2/day for 5months. During the treatment the number and size of hemangio~rnas were markedly r'duced. (Kor J Dermatol 1996;34(6): 1039-1043)
실신을 동반한 우측 관상동맥굴에서 기인한 좌관상동맥의 기형의
한대희 ( Dae Hee Hahn ),고현철 ( Hyeon Cheol Koh ),홍정운 ( Jung Un Hong ),박기수 ( Gi Soo Park ),김경중 ( Gyung Jung Kim ),박경득 ( Kyung Deuk Park ),이상칠 ( Sang Chil Lee ) 대한내과학회 2014 대한내과학회지 Vol.87 No.6
Congenital anomalies of the coronary artery are associated with various symptoms including syncope, myocardial ischemia, and sudden cardiac death. The abnormality depends on the adjacent structure and pathway of the coronary artery. Most patients with an anomalous left coronary artery that arises from a right coronary sinus of the valsalva have no symptoms and are usually diagnosed at autopsy. Therefore, their first symptom might present as sudden death, particularly when the left coronary arterial course is between the aorta and the pulmonary trunk. Symptomatic patients could be diagnosed early with an anomalous coronary artery, and the risk of fatal events could be decreased by surgical correction. Here, we report the case of 62-year-old male who experienced a first episode of syncope with an anomalous left coronary artery arising from the right sinus of the valsalva with a separate orifice from the right coronary artery. He is alive and in good health receiving medical treatment, and has had no medical events for over 2 years. (Korean J Med 2014,87:722-727)