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개에서 xylazine으로 유발한 서맥에 대한 내관혈(PC-6) 뜸요법의 회복 효과
박성민,박형진,서경원,송근호,Park, Seong-Min,Park, Hyung-Jin,Seo, Kyoung-Won,Song, Kun-Ho 대한수의학회 2013 大韓獸醫學會誌 Vol.53 No.2
This study was performed to investigate the effect of Nei Guan (PC-6) moxibustion stimulation on artificial bradycardia of dogs. Xylazine was injected for inducing bradycardia. Rectal temperature, systolic blood pressure, respiratory rate, heart rate were recorded every 10 minutes for 120 minutes. Systolic blood pressure significantly increased on 40 min (p < 0.05) after xylazine injection, compared with those of control group. Heart rate significantly increased on 40 min (p < 0.01), 50 min (p < 0.01), 60 min (p < 0.01), 70 min (p < 0.01), 80 min (p < 0.01), 100 min (p < 0.01), 120min (p < 0.01) after xylazine injection, compared with those of control group. In conclusion, moxibustion of Nei Guan (PC-6) showed recovery effect in xylazine induced bradycardia in dogs.
전립선암 환자에서 Leuprolide Acetate에 의한 이물육아종
박성민 ( Sung-min Park ),김정민 ( Jeong-min Kim ),김건욱 ( Gun-wook Kim ),문제호 ( Je-ho Mun ),송마가렛 ( Margaret Song ),김훈수 ( Hoon-soo Kim ),김병수 ( Byung-soo Kim ),김문범 ( Moon-bum Kim ),고현창 ( Hyun-chang Ko ) 대한피부과학회 2016 대한피부과학회지 Vol.54 No.6
Leuprolide acetate is an established luteinizing hormone-releasing hormone (LHRH) agonist used as a first-line treatment in advanced prostate cancer. An 80-year-old man presented with a localized erythematous patch with an indurated plaque and nodule and pustules on the left upper arm. The patient had been treated for metastatic prostate cancer with subcutaneous injections of leuprolide acetate 18 months previously. Histopathologic findings revealed granulomas with multinucleated giant cells from the dermis to the subcutaneous fat layer. The granuloma contained numerous round vacuoles. Cultures from the tissue for bacteria, fungi, and mycobacteria were all negative. The diagnosis of leuprolide acetate-induced foreign body granuloma was made by clinicopathologic findings. Various theories on the mechanism of local reactions to leuprolide have been suggested. The formation of granulomas may be related to the poly (lactic-co-glycolic acid) polymers or leuprolide itself. The depth of injection could have also contributed; therefore, intramuscular injection is recommended to minimize granuloma formation. To the best of our knowledge, there has been no reported case of leuprolide-induced foreign body granuloma in a patient with prostate cancer in the Korean literature. Dermatologists need to know that leuprolide acetate depot injection may cause a granulomatous reaction. (Korean J Dermatol 2016;54(6):477∼480)
중등도-중증의 한국인 건선 환자에서 Ustekinumab의 효과와 안전성에 관한 연구
박성민 ( Sung Min Park ),김정민 ( Jeong Min Kim ),김건욱 ( Gun Wook Kim ),문제호 ( Je Ho Mun ),송마가렛 ( Margaret Song ),김훈수 ( Hoon Soo Kim ),고현창 ( Hyun Chang Ko ),김문범 ( Moon Bum Kim ),김병수 ( Byung Soo Kim ) 대한피부과학회 2015 대한피부과학회지 Vol.53 No.8
Background: Ustekinumab, a fully human monoclonal immunoglobulin antibody that targets the P40 subunit shared by interleukin (IL)-12 and IL-23 has emerged as a promising treatment for moderate to severe psoriasis. However, to date, there are no ‘clinical practice setting’ data on ustekinumab in Korean patients with psoriasis. Objective: To assess the clinical efficacy and safety of ustekinumab in Korean patients with psoriasis. Methods: Prospective data were gathered during the follow-ups of 34 consecutive chronic plaque psoriasis patientstreated with ustekinumab for a minimum of 16 weeks at a single referral center. Patients’ demographics, Psoriasis Area Severity Index (PASI) score, Physicians’ Global Assessment (PGA), Dermatologic Life Quality Index (DLQI), and adverse events were investigated. Results: The mean PASI score significantly decreased after the first administration of ustekinumab (paired t-test, p< 0.05). Twenty-one of 34 patients (61.8%) had obtained near-complete clearance (PASI 90) upon the last follow-up visit. No unexpected adverse events other than herpes zoster and elevated liver enzymes were observed. Conclusion: Ustekinumab can be of benefit in the treatment of Korean psoriasis patients, as it was associated with a rapid and satisfactory response and was well tolerated. (Korean J Dermatol 2015;53(8):617∼622)
Mycoplasma pneumoniae에 의해 발생한 피부발진과 점막염
박성민 ( Sung-min Park ),김정민 ( Jeong-min Kim ),김건욱 ( Gun-wook Kim ),문제호 ( Je-ho Mun ),송마가렛 ( Margaret Song ),김훈수 ( Hoon-soo Kim ),김병수 ( Byung-soo Kim ),김문범 ( Moon-bum Kim ),고현창 ( Hyun-chang Ko ) 대한피부과학회 2017 大韓皮膚科學會誌 Vol.55 No.3
Mycoplasma pneumoniae (M. pneumoniae) is one of the most common causes of respiratory tract infections in pediatric and adult populations worldwide. M. pneumoniae is also associated with extrapulmonary complications, such as mucocutaneous eruptions. In dermatologic disorders, M. pneumoniae infection is known to be associated with erythema multiforme and Stevens-Johnson syndrome in children and young adults. Recently, several cases with M. pneumoniae-associated mucositis, which lacks typical target lesions, have been reported. The term Mycoplasmainduced rash and mucositis was suggested as a revised version of the term, Mycoplasma pneumoniae-associated mucocutaneous disease, which previously included erythema multiforme and Stevens-Johnsons syndrome. This revision helps to distinguish Mycoplasma-induced rash and mucositis, which has a distinct morphology, mild disease course, and potentially important clinical implications regarding treatment. Herein, we report a patient with Mycoplasma-induced rash and mucositis. (Korean J Dermatol 2017;55(3):186∼190)
결합조직모반만을 보인 환자에서 유전자검사를 통해 진단된 결절경화증
박성민 ( Sung-min Park ),김정민 ( Jeong-min Kim ),김건욱 ( Gun-wook Kim ),문제호 ( Jeho Mun ),송마가렛 ( Margaret Song ),김훈수 ( Hoon-soo Kim ),고현창 ( Hyun-chang Ko ),김병수 ( Byung-soo Kim ),김문범 ( Moon-bum Kim ) 대한피부과학회 2017 大韓皮膚科學會誌 Vol.55 No.1
Tuberous sclerosis complex (TSC) is a neurocutaneous disorder with variable manifestations. The diagnosis is based on clinical criteria, and is divided into definite, probable, and possible TSC. If patients present with mild symptoms, clinicians may hesitate to perform further evaluations because of the high economic burden. A 16-year-old male presented with multiple skin-colored papules on the lower back and buttock. The histopathologic findings were compatible with connective tissue nevi (CTN). No other findings were observed with the exception of one hypomelanotic macule on the left shin. As the patient`s parents wished to confirm the diagnosis, genetic testing was performed, and a TSC1 gene mutation was detected. With this genetic result, further evaluations were performed without hesitation. Genetic testing is a sensitive and specific modality for the diagnosis of TSC. We report a case of TSC presenting with CTN only, in which genetic testing was very useful to confirm the diagnosis and to determine the appropriateness of further high-cost studies. (Korean J Dermatol 2017;55(1):56∼59)
각종 간질환 및 수혈 경력 환자에서 C 형 간염 바이러스 항체의 발현 양상
박성민(Sung Min Park),주기중(Kee Joong Ju),이창환(Chang Hwan Lee),심영웅(Young Woong Shim),송갑영(Kap Young Song) 대한내과학회 1993 대한내과학회지 Vol.45 No.2
Background: We studied the prevalence of Hepatitis C viruses in various liver diseases in Korea using recombinant viral antigen (C 100-3) to evaluate its etiological significance and routes of transmission. Methods: A total of 256 patients with chronic renal failure who experienced transfusion or hepatocellular disease were tested for serum HBsAg & Ab, HBcAb, Anti-HCV, AST, ALT and some were performed liver biosy for diagnostic purpose. The 46 cases of acute hepatitis, 78 cases of chronic hepatitis, 25 cases of liver cirrhosis, 30 cases of hepatocellular carcinoma, 15 cases of hemodyalysis patients, 62 cases of hepatitis B virus carrier were studied. Results: 1) There were 1.2% Anti-HCV positive patients among 256 cases. Among them there were 32.0% of liver cirrhosis, 16.7% of hepatocellular carcinoma, 20.0% of hemodialysis patients, 8.7% of acute hepatitis, 11.5% of chronic hepatitis, 4.8% of hepatitis B virus carrier (Table 1). 2) Among 184 cases of HBsAg positive patient, 20 cases (10.9%) were Anti-HCV positive and among 72 cases of HBsAg negative patients, 12 cases (16.7%) were Anti-HCV positive (Table 2, 3). 3) Among 32 cases of Anti-HCV positive patients, 20 cases (62.5%) were HBsAg positive and 12 cases were negative (Table 4). 4) Among Anti-HCV positive and HBsAg negative patients, the higher positive response of Anti-HCV were noted in patients with HBcAb positive and increased AST and ALT (Table 5). 5) Among Anti-HCV positive patients, the 65.4% were related to transfusion or acupuncture (Table 6). Conclusion: This study shows that further research for the development of more sensitive and specific diagnostic method for hepatitis C and thorough follow up study for its routes of transmission are needed.
Case Report : Megalencephaly-capillary Malformation Syndrome
박성민 ( Sung-min Park ),김건욱 ( Gun-wook Kim ),조현호 ( Hyun-ho Cho ),김원정 ( Won-jeong Kim ),문제호 ( Je-ho Mun ),송마가렛 ( Margaret Song ),김훈수 ( Hoon-soo Kim ),김병수 ( Byung-soo Kim ),김문범 ( Moon-bum Kim ),고현창 ( Hyun 대한피부과학회 2015 大韓皮膚科學會誌 Vol.53 No.7
Megalencephaly-capillary malformation syndrome is a disorder characterized by megalencephaly or hemimegalencephaly, focal or generalized somatic overgrowth, and vascular malformations. Other characteristic features are neonatal hypotonia, hydrocephalus, developmental delay, syndactyly/polydactyly, frontal bossing, and connective tissue dysplasia. Previously reported patients exhibit wide phenotypic variability in clinical and neuroradiological findings. Differential diagnosis may be challenging for clinicians due to other similar neurocutaneous syndromes. Herein, we report an 11-month-old male infant that presented with extensive, diffuse, reticulated, erythematous patches on his face, trunk, and extremities. Physical examination revealed an increased head circumference (>97 percentile), frontal bossing, hypertrophy of the right arm and leg, and syndactyly on both feet. Borderline developmental delay was identified, and magnetic resonance imaging of the brain revealed an enlarged right cerebral hemisphere and non-obstructive ventriculomegaly. To our knowledge, this is the first report of megalencephalycapillary malformation syndrome in Korean literature. (Korean J Dermatol 2015;53(7):546∼551)
박성민 ( Sung Min Park ),조현호 ( Hyun Ho Cho ),김원정 ( Won Jeong Kim ),문제호 ( Je Ho Mun ),송마가렛 ( Margaret Song ),김훈수 ( Hoon Soo Kim ),김병수 ( Byung Soo Kim ),김문범 ( Moon Bum Kim ),고현창 ( Hyun Chang Ko ) 대한피부과학회 2014 대한피부과학회지 Vol.52 No.5
Subcutaneous sarcoidosis is rare and presents as tender or painless nodules that mostly occur on the extremities. We report a 47-year-old female patient presenting with a 1-month history of multiple asymptomatic subcutaneous nodules on the extremities. The patient had a history of myasthenia gravis for 5 years. Histopathological findings from the subcutaneous nodules showed non-caseating granulomas compatible with sarcoidosis. On inspection for internal involvement, pulmonary sarcoidosis was also detected by chest computed tomography, bronchoalveolar lavage, and transbronchial lung biopsy. The concurrence of sarcoidosis and myasthenia gravis is rare and has not been reported in the Korean literature. It may be supposed that the concurrence of these 2 separate entities is coincidental, but it has been reported that myasthenia gravis with specific antibodies is associated with sarcoidosis. This suggests that a common immunopathogenic mechanism may exist between these 2 diseases. (Korean J Dermatol 2014;52(5):333∼336)