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      • SCOPUSKCI등재

        중복 감염된 표재성 진균증의 균학적 및 면역학적 연구

        이기왕(Ky Wang Lee),김홍직(Hong Jig Kim) 대한피부과학회 1984 大韓皮膚科學會誌 Vol.22 No.4

        This study was to investigate the relationship between the causative strains and lesional sites and to detect the status of cell mediated immunity in the patients with concurrent fungal infections. The authors performed mycological and immunologic studies on 32 patients with concurrent fungal infections who had visited the dermatologic clinic of Soonchunhyang University HospitaI from July 1982 to June 1983. The results were summarized as follows: It was 18 cases that had the positive cultures in all the lesion sites. Among them 12 cases obtained the same causative strains in all lesions of each patierit. The cultured dermatophytes were Trichophyton rubrum, 10 stains, Trichophyton mentagrophytes, 2 strains. 2. Positive inrnediate hypersitivity reaction was observed only in patients with concurrent fungal infection by trichophytin (87. 5%). 3. For the delayed hypersensitivity reaction, the mean skin reaction scores to PPD, candidin, trichophtin were l. 58, 2. 78, 0. 66 respectively in 32 patients with concurrent fungal infection and 1. 89, 2. 47, l. 50 respectively in 17 controls, but the statistically significancies were only in trichophytin (p<0. 05). 4. The mean percentage of total and active T cell counts in peripheraJ blood were 55. 2%, 23. 9% respectively in 18patients, and 64,0%, 29. 8% in controls(p<0. 05). There was a significant decrease of T-cell count in patients with concurrent fungal infections.

      • SCOPUSKCI등재

        선천성 부신 무형성증에 의한 피부 과색소침착증

        김홍직(Hong Jig Kim),김영근(Young Keun Kim),이기왕(Ky Wang Lee) 대한피부과학회 1985 대한피부과학회지 Vol.23 No.3

        In adrenal insufficiency, recognition of the disease in its earlier phases may present a real challenge. The disease, if unrecognized and untreated, carries an almost uniformly poor and frequently fatal prognosis. We report a rare case of congenital adrenal aplasia accompanied by hyperpigmentation on the whole body surface. The diagnosis was confirmed by ACTH stimulation t st and autopsy findings,

      • 결절성 열모증(Trichorrhexis nodosa) 2예

        김홍직,이기왕 순천향대학교 1984 논문집 Vol.7 No.2

        Trichorrhexis nodosa is a distinctive response of the hair shaft to physical or chemical trauma, characterized by the development of node like swellings through which the shaft readily fractures. We experienced two cases of trichorrhexis nodosa. Nodular swelling of the affected hair showed longitudinal fissures and fractures in the cortox. At the site of fracture, a paint-brush like effect was seen.

      • Reiter 증후군 1예

        김홍직,이기왕 순천향대학교 1984 논문집 Vol.7 No.2

        We experienced a case of venereal form of Reiter's syndrome developed in 30 years old non-married woman. She had been suffered from arthritiis, nonspecific urethritis, conjunctivitis and keratoderma blenorrhagica. She was treated with bed rest, short leg splint, Aspirin, corticosteroid for arthritis, tetracycline for nonspecific urethritis, eye drop containing antibiotics and corticosteroid for conjunctivitis and corticosteroid ointment for skin lesion. She was completely cleared 2 months later and the disease was not relapsed for 1 year of follow up period.

      • 피지선 모반 증후군 1예

        김홍직,이기왕 순천향대학교 1984 논문집 Vol.7 No.3

        Nevus sebaceus is first described by Jadassohn and commonly develops on scalp or face as a single lesion. But it may be multiple and assiciated with convulsion, mental retardation, neurologic defects and skeletal defects. It is called nevus sebaceus syndrome which may be considered as a neurocutaneous syndrome when nevus sebaceus is associated with disorders of central nervous system. We experienced a case which was suggested as a nevus sebaceus syndrome because multiple nevus sebaceus were located on scalp, face and chest in a 5-days male newborn but neurologic symptoms were not showed until then.

      • 투명세포 한선종 1례

        김홍직,김영근,이기왕 순천향대학교 1984 논문집 Vol.7 No.4

        Clear cell hidradenoma, now regarded as an eccrine sweat gland tumor on the basis of its enzyme histochemical and electron microscopic features, occurs as a solitary tumor in most instances. The tumors present themselves as intradermal nodules and in most instances measure between 5mm and 30mm in diameter, although they may be larger. Microscopically the tumor composed of characteristic clear epithelial cells which are focally arranged in glandular and cystic patterns. We report a case of clear hidradenoma in a 46-year-old housewife who had suffered from a tumor on her retroauricular area for 6 months. The tumor was a pedunculated soft mass, 1×1×0.7cm in size, and histopathologic findings showed typical clear cell hidradenoma.

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