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나건연 ( Gun Yoen Na ),김용현 ( Young Hyeon Kim ),민복기 ( Pok Kee Min ),황성주 ( Sung Joo Hwang ) 대한피부과학회 1996 대한피부과학회지 Vol.34 No.5
A 6-month-old female infant pre~sented with multiple, slightly depressed pea-sized erythematous macules on. the abdomen and the chest since birth, which together with obese, short stature, short neck, and round face suggested Albrights hereditary osteodystrophy(AHO). Some of the lesions were palpable as hard nodules or plaques in deep dermis. After 3 months follow up, the erythem- atous hue faded out, subcutaneous nodules and plaques enlarged. Skin biopsy specirnen demonstrated a bone formation in deep dermis. Serum calcium and phosphorus levels were lower and upper normal ranges, respectively and serum parathyroid hormone was increased in 69.1 pg/ml (normal, 9-55pg/ml). As pseudohypoparathyroidism including this case mostly exhibit characteristic morphologic features of AHO, the subcutaneous ossification may be a presenting feature. (Kor J Dermatol 1996;34(5): 842-846)
남성형 탈모증 환자에서 시행한 모속이식술 52예에 대한 치료효과 분석
민복기,황성주,김도원,정상립,김정철,나건연 ( Pok Kee Min,Sung Joo Hwang,Do Won Kim,Sang Lip Chung,Jung Chul Kim,Gun Yoen Na ) 대한피부과학회 1997 대한피부과학회지 Vol.35 No.5
Background: There have been numerous methods to treat androgenetic alopecia but few methods to treat it effectively and permanently. Objective : The purpose of this study was to evaluate bundle hair grafting as an effective treatment for patients with androgenetic alopecia. Methods : Bundle hair grafiing was performed on 52 patients with androgenetic alopecia who had visited the department of dermatology, Kyungpook National University Hospital and Fatima Hospital. Questionaires regarding cosmetic satisfaction, side effects and general efficacy were recorded by patients themselves one year after hair grafting. Results : The results are as follows : 1. The loss of transplanted hair was most common during the third week(48.1%) after hair grafting. 2. The regrowth of the hair on the recipient site was most common during the 4th month(59.6 %) after the hair graft. 3. Bundle grafting afforded excellent cosmetic satisfaction even after one session in the alopecic area, 4. Facial edema, temporary sensory loss on the donor site, folliculitis and small pitted scarring were seen 19.2%, 5.8%, 1.9% and 3.8% of patients, respectively. 5. The disadvantages were the time necessary to carry out the procedure and the need for an experienced operator and assistants. Conclusion : We concluded that bundle hair grafting was an effective and safe therapeutic method for patients with androgenetic alopecia. (Korean J Dermatol 1997;35(5): 893-901)
Methotrexate로 치료한 타카야수 동맥염에 동반된 괴저성 농피증
김종근 ( Jong Keun Kim ),서준혁 ( Jun Hyuk Seo ),윤준철 ( Jun Cheol Yoon ),박도회 ( Do Hwae Park ),조민재 ( Min Jae Jo ),이찬우 ( Chan Woo Lee ),백애란 ( Ae Lan Paik ),민복기 ( Pok Kee Min ),나건연 ( Gun Yoen Na ),오동호 ( Dong Ho 대한류마티스학회 2006 대한류마티스학회지 Vol.13 No.1
Pyoderma gangrenosum (PG) is a vasculitic process, often associated with systemic diseases, including Takayasu`s arteritis (TA), rheumatoid arthritis, and inflammatory bowel disease. Most cases of PG associated with TA have been observed in Japan. However, this association is not commonly observed in North American and European patients. PG is often refractory to therapy, requiring high dosages of glucocorticoids. Here, we describe a case of recalcitrant PG that was associated with TA and successfully treated with methotrexate.
조영재 ( Young Jae Cho ),이상우 ( Sang Woo Lee ),임성택 ( Seung Taek Lim ),김종근 ( Jong Keun Kim ),김영호 ( Young Ho Kim ),이찬우 ( Chan Woo Lee ),오동호 ( Dong Ho Oh ),민복기 ( Pok Kee Min ),나건연 ( Gun Yoen Na ),박지영 ( Ji Yo 대한류마티스학회 2004 대한류마티스학회지 Vol.11 No.3
Sweet`s syndrome is an uncommon reactive dermatosis characterized by fever, poly-morphonuclear leukocytosis, painful erythematous cutaneous plaques and dense dermal infiltrate of neutrophils at the skin lesions. Unlike Sweet`s syndrome associated with patients with malignancies, autoimmune diseases, antecedent infectons-most commonly the upper respiratory infections, it is reported to be rarely associated with systemic lupus erythematosus (SLE). Here we report a rare case of young female with Sweet`s syndrome and SLE presenting with high fever.