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한을희(Eul Hee Han),권경술(Kyung Sool Kwon),정태안(Tae Ahn Chung) 대한피부과학회 1983 大韓皮膚科學會誌 Vol.21 No.1
Human sparganosis is not uncommon and over 60 cases are reported in Korea but the case infested with multiple spargana is rare. The case we are reporting here is a 33 year-old Korean male having had an abscess and several bean-sized nodules on the left thigh. The patient had the history of eating frogs as a tonic food 3 years ago. Five spargana were removed from the lesions by surgical excision. Two of them were alive and other three were degenerated or calcified.
권경술(Kyung Sool Kwon),한을희(Eul Hee Han),정태안(Tae Ahn Chung),임명규(Myeong Kyoo Lim),박성귀(Sung Kwi Park) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.2
A case report of a 60 year-old man with lichen aureus of leg is presented. Clinically the solitary golden to purple colored patch consists of lichenoid papules, plsque, and mild petechiae around the lesion, and the histology reveals a dense and bandlike infiltrate hugging thepidermis. It consists of lymphocytes, histiocytes, eosinophils, and many extravasated erythrocytes and hemosiderin in dermis, but a few red cells and increased melanin pigment can also be seen in the epidermis. The eruption is mildly itchy and has been present 6 months. (Kor J Dermatol 1994; 32(2): 342-315)
권경술(Kyung Sool Kwon),한을희(Eul Hee Han),정태안(Tae Ahn Chung),신항계(Hang Kye Shin),김천기(Cheon Gi Kim) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.1
A 51-year-old female developed a distinctive perioral rash, conisting of discrete or confluent erythematous papules for one and a half years. Histopathologic examiriation revealed upper dermal granulomas admixed with lymphoytes. Pieces of hair shaft were staincd peri-dish by AFB in the center of granuloma, which might play a role in the formation of the granuloma She also had used corticosteroid ointment intermittently duririg this time. There were no associated systemic abnormalities. The lesions resolved after two month treatment with oral corticosteroid and tetrac cline. (Kor J Dermatol 1994; 32(1): 182-185)
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)
어린선양 사르코이드증 ( Ichthyosiform sarcoidosis )
최석주(Suk Joo Choi),한을희(Eul Hee Han),권경술(Kyung Sool Kwon),정태안(Tae Ahn Chung) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.1
Although acquired ichthyosis has been associated with a number of systemic illnesses, an association with sarcoidosis has rarely been reported. We report a patient with aquired ichthyosis of the lower and upper extrimities whose diagnosis of cutaneous sarcoidosis was confirmed by histologic examination. Systemic involvement in the patient revealed occular, pulmonary and nerve disease. A diagnosis of sarcoidosis must be considered when a patient presents with acquired ichthyosis. (Kor J Dermatol 1994; 32(1): 172-176)
범발성 색소이상증 - 4대에 걸쳐 상염색체 우성 유전 양상을 보인 1가족예 -
신항계(Hang Kye Shin),한을희(Eul Hee Han),권경술(Kyung Sool Kwon),정태안(Tae Ahn Chung) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.3
Dyschromatosis universalis hereditaria is a rare pigmentary disorder characterized by widespread mothed hyperpigmentation and hypopigmentation. We report a 40-year-old male patient with numerous hyperpigmenter, and hypopigmented macules all over the body except on the palms and soles. The family history revealed similar pigmentary changes in 5 other members through 4 generations, and we could guess the hereditary pattern of the disease of this family to be autosomal dominant inheritance. (Kor J Dermatol 1994; 32(3): 493-497)
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
신항계(Hang Kye Shin),한을희(Eul Hee Han),권경술(Kyung Sool Kwon),정태안(Tae Ahn Chung) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.3
Cerebriform intradermal melanocytic nevus is a cause of cutis veticis gyrata, a morphologic term which describes the hypertrophy and folding of the skin, typically occurring on the scslp, to present a gyrate or cerebriform appearance. We report a 37-year-old woman with a 17 x 22cm soft, convoluted mass over most of the occipital, parietal, and temporal scalp. At birth, she had a small brownish macide on the occipital scalp that enlarged to form this extensive lesion. Histologically, nests of nevus cells were shown in the upper and the mid dermis. (Kor J Oermatol 1994; 32(3): 488-492)
김천기(Cheon Gi Kim),차형기(Hyung Gi Cha),한을희(Eul Hee Han),권경술(Kyung Sool Kwon),정태안(Tae Ahn Chung) 대한피부과학회 1994 대한피부과학회지 Vol.32 No.2
Basal cell carcinoma(BCC) is the most common human malignancy. It involves the face and neck most frequently. However, BCC can very rarely occur on external glenitalia such as scrotum and vulva. We report two cases of serotal and vulvar BCCs in a 67 year old imale and a 43 year old female. He suffered from well defineril erythematous to violet colored plaque with central erosion on the left scrotum for 5 years. She had a brown black colored plaque on the left vulva for 8 years. They did not show any metastatic foci from g!rimary cutaneous lesions, and underwent surgical excision and curettage respectively. (Kor J Derrinatol 1994; 32(2): 342-346)
권경술,한을희,정태안 대한피부과학회 1982 大韓皮膚科學會誌 Vol.20 No.3
We present two cases of linear lichen simplex chronicus. One is a 44-year-old male patient who had a linear licbenified patch on the left upper extremity, and the other is a 45-year-old female patient who had linear pruriginous nodules on the right lower extremity. The one is coincidental with localized lichen simplex chronicus, the other is coincidental with prurigo nodularis histopathologically.