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이준호(Joon Ho Lee),한을희(Eul Hee Han),권경술(Kyung Sool Kwon),정태안(Tae Ahn Chung) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.1
Cytophagic histiocytic psnniculitis is a histiocytic disorder which is characterized by recurrent subcutaneous nodules, fever, pancytopenia, and abnormal hepatocyte funciion. Most patients had systemic involvement with hepatosplenomegsly and psncytopenia
항생제 피내반응 검사부위에 발생한 Mycobacterium fortuitum 감염증
이준호(Joon Ho Lee),문두찬(Doo Chan Moon),권경술(Kyung Sool Kwon),정태안(Tae Han Chung) 대한피부과학회 1993 대한피부과학회지 Vol.31 No.5
Cutaneous mycobacterial infection can occur with Mycobacterium tube culosis or other mycobacterial agents. The commonest of the group IV rapidly growing mycobacteia Mycobacterium fortuitum, has widespread distribution in natur, and is an uncommon causative agent of human mycobacterial infection. We report herein a case of Mycobacterium fortuitum infection follcwiiig an antibiotics susceptibility test. This 24-year-old man suffered fram ulcerative itchy nodules on the left forearm where the antibiotics susceptibility test was don. The skin biopsy specimen revealedly. iphohistiocytic granulomatous infiltration in the dermis. Culture of the tissue specimen revealed rapicly growing yellowish colonies, which was isolated to Mycobacoterium fortuitum. Among 3 biovariants of M. fortuitum, our case was revealed to he biovariant fortuiiam: Surgical excision was performed followed by the administration of antiliiiitics, and no sign of relapse was noted until now, 1 year since. (Kor J Dermatol 1993;31(5): 769-774)
경화 위축성 태선과 경피증의 감별진단에 있어서 렉틴의 의의
이준호,문두찬,권경술,정태안 ( Joon Ho Lee,Doo Chan Moon,Kyung Sool Kwon,Tae Ahn Chung ) 대한피부과학회 1993 大韓皮膚科學會誌 Vol.31 No.3
Background : Differential diagnosis of lichen sclerosus et atrophicus( SA) and scleroderma is occasionally difficult. Objective : The purpose of this study was to attempt differentiation between the two diseases using imrnunohistochemical stain and lectins. Methods : Paraffin-embeddred sections of 4 cases of LSA and 11 cases of scleroderma were evaluated for this study. Using lectins, such as peanut agglutinin(PNA), siybean agglutinin(SBA), Ulex europaeus agglutinin-I(UEA-I) and Dolichos biflorus agglutinin(DBA) and the avidin-biotin-peroxi-dase complex(ABC) technique, differential lectin binding patterns betv een the two diseases were examined. Results : In the case of LSA, PNA and SBA stained the upper and lower spinous layer of the epidermis, and UEA I also stained the spinous layer of the epidermis weakly, but no DBA was stained. In the case of scleroderma, PNA stained not only the spinous layer but also the basal layer, SBA stained the upper half of the spinous layer but not the lower half of the pinous layer of epidermis. But UEA-I stained the vascular endothelial cells of dermis instead of epidermis, and DBA stained only the basal layer of epidermis. Conclusion : Staining of these 4 lectins on paraffin-embedded sectians using ABC teehnique could be helpful in differenting LSA and scleroderma. (Kor J Dermatol 1993; 31(3): 329-336)
권경술(Kyung Sool Kwon),한을희(Eul Hee Han),정태안(Tae Ahn Chung),최석주(Suk Joo Choi),이준호(Joon Ho Lee) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.1
A 28-year-old female devei,oped five rice-sized erythematous telaniectatic solid papules of her left side of cheek and numerous light brownish flat papules of her face two years before visiting our department of dermatology. Biopsy results of the erythematous papule vere dermal infiltration by well-differentiated, however, somewhat atypical and varying sized plasma cells involving epidermis, and the flat papule was that of verwca plana. Bone marrow aspirate was essentially normal. Primary cutaneous plasmacytoma is a rare disease. A significant proportion of patients with this ent on to develop systemic disease with a poor prognosis. Our patient was not treatead, bit only excised partially for biopsy. All skin lesions involuted two years later spontaneously and rema ns well until now six years later without recurring. (Kor J Dermatol 1994; 32(1): 144-148)