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정석준 ( Suck Joon Jung ),승나르 ( Na Reu Seung ),서영주 ( Young Ju Seo ),박은주 ( Eun Ju Park ),김철우 ( Chul Woo Kim ),조희진 ( Hee Jin Cho ),김광호 ( Kwang Ho Kim ),김광중 ( Kwang Joong Kim ) 대한피부과학회 2008 대한피부과학회지 Vol.46 No.7
Pilar sheath acanthoma is a rare, benign follicular hamartoma commonly affecting middle-aged and elderly individuals. It is characterized by a small, solitary, skin-colored papule situated on the head and neck, particularly around the upper lip. The lesion shares some features with trichofolliculoma and dilated pore of Winer, so it should be differentiated from these. Cytokeratin (CK) is a useful marker for studying the origin of epithelial tumors. We report a case of pilar sheath acanthoma which originated from outer root sheath using CK. (Korean J Dermatol 2008;46(7):955~957)
정석준 ( Suck Joon Jung ),승나르 ( Na Reu Seung ),서영주 ( Yeong Ju Seo ),박은주 ( Eun Ju Park ),김철우 ( Chul Woo Kim ),조희진 ( Hee Jin Cho ),김광호 ( Kwang Ho Kim ),김광중 ( Kwang Joong Kim ) 대한피부과학회 2007 대한피부과학회지 Vol.45 No.12
Estrogen dermatitis is a rare cutaneous disorder characterized by recurrent cyclic eruptions during the luteal phase of the menstrual cycle. The clinical manifestations include pruritus, urticaria, vesicles, papules and eczematous eruptions. A 22-year-old female patient presented with a skin lesion on the back of 6 years periodic duration. She had been recurrently suffering from pruritic eruptions that appear during the luteal phase of the menstrual cycle and resolve after menses. An intradermal skin test to estrogen showed a positive result, but showed negative results to progesterone. After antiestrogen tamoxifen therapy, the lesions were found to have significantly improved. (Korean J Dermatol 2007;45(12):1291∼1293)
이산화탄소 레이저를 이용한 표재성 피부지방종양모반의 치료
정석준 ( Suck Joon Jung ),김현준 ( Hyun Joon Kim ),서영주 ( Yeong Ju Seo ),박은주 ( Eun Ju Park ),김철우 ( Chul Woo Kim ),김광호 ( Kwang Ho Kim ),김광중 ( Kwang Joong Kim ) 대한피부과학회 2007 대한피부과학회지 Vol.45 No.10
Nevus lipomatosus cutaneous superficialis (NLCS) is a fairly uncommon lesion characterized by ectopic adipose tissue in the dermis. It presents as soft yellowish papules or cerebriform plaques occurring usually on the buttock or thigh with a wrinkled surface. We report a case of NLCS in 38-year-old female who presented reddish brown colored cerebriform tumors on her buttock and was treated by CO2 Laser. To our knowledge this is the first case of NLCS treated by CO2 Laser, path of except by excisional surgery. (Korean J Dermatol 2007;45(10):1093∼1095)
김현준 ( Hyun Joon Kim ),정석준 ( Suck Joon Jung ),박은주 ( Eun Joo Park ),김철우 ( Chul Woo Kim ),조희진 ( Hee Jin Jo ),김광호 ( Kwang Ho Kim ),김광중 ( Kwang Joong Kim ) 대한피부과학회 2007 대한피부과학회지 Vol.45 No.1
Papular elastorrhexis is a rare disorder in which children or adolescents present with asymptomatic, non-follicular, 1~5 mm firm white papules on the trunk and extremities. Histologically, there are focal areas of collagen homogenization with decreased and fragmented elastic fibers. Most reported cases are sporadic, but familial occurrence has been described. We report an uncommon and interesting case of papular elastorrhexis in both a brother and sister. (Korean J Dermatol 2007;45(1):82~86)
승나르 ( Na Reu Seung ),정석준 ( Suck Joon Jung ),박은주 ( Eun Joo Park ),김철우 ( Chul Woo Kim ),조희진 ( Hee Jin Cho ),김광호 ( Kwang Ho Kim ),김광중 ( Kwang Joong Kim ) 대한피부과학회 2007 대한피부과학회지 Vol.45 No.5
Cutaneous, diffuse, large B-cell lymphoma (DLBCL) is characterized by a diffuse dermal infiltration which is composed of large centroblasts and immunoblasts. It is subdivided into a primary form arising from the skin and a secondary form which is metastasized from the lymph node. Secondary DLBCL has a more aggressive clinical course than the primary form. We report a 39-year-old female patient who presented with a 2 cm sized, erythematous, subcutaneous nodule on her left upper arm. She had been treated for brain-diffuse, large B-cell lymphoma which occurred 5 years before. The histopathologic and immunohistochemical examinations of the skin lesion also showed diffuse, large, B-cell lymphoma. (Korean J Dermatol 2007;45(5):458~461)
Tretinoin 국소 도포로 호전된 비립종양 특발성 피부 석회증
최우진 ( Woo Jin Choi ),정석준 ( Suck Joon Jung ),서영주 ( Yeong Ju Seo ),박은주 ( Eun Ju Park ),조희진 ( Hee Jin Jo ),김광호 ( Kwang Ho Kim ),김광중 ( Kwang Joong Kim ) 대한피부과학회 2008 대한피부과학회지 Vol.46 No.12
Milia-like idiopathic calcinosis cutis is a rare entity. It is characterized by micronodular, whitish papules resembling milia. Histopathological examination shows small nodular foci of calcium within the superficial dermis, which are surrounded by thick collagen and inflammatory cells. Although the pathogenesis and treatment remain unclear, spontaneous resolution of the lesions may occur. We report a case of milia-like idiopathic calcinosis cutis in a 7-year-old girl who improved after treatment with tretinoin cream. (Korean J Dermatol 2008;46(12):1640∼1643)