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한국인에서의 악성 흑생종에 대한 임상 및 병리 조직학적 연구 - 대한피부과학회 피부병리연구분과위원회 공동연구 -
이미우 ( Mi-Woo Lee ),고재경 ( Jai-Kyoung Koh ),권경술 ( Kyung-Sool Kwon ),김낙인 ( Nack-In Kim ),김상원 ( Sang-Won Kim ),김수남 ( Soo-Nam Kim ),김방순 ( Bang-Soon Kim ),김유찬 ( You-Chan Kim ),김종민 ( Jong-Min Kim ),명기범 ( Ki- 대한피부과학회 2003 대한피부과학회지 Vol.41 No.1
Backgorund ; Malignant melanoma in Korean has been increasing as in other countries, but there is no nationwide survey of malignant melanoma in Korea. Objective : The aim of this study was to document the clinical and histopathological features of cutaneo
한국인에서의 피부 림프종의 임상 및 병리조직학적 연구 - 대한피부과학회 피부병리연구분과위원회 공동연구 -
이미우 ( Mi-Woo Lee ),고재경 ( Jai-Kyoung Koh ),권경술 ( Kyung-Sool Kwon ),김낙인 ( Nack-In Kim ),김상원 ( Sang-Won Kim ),김수남 ( Soo-Nam Kim ),김방순 ( Bang-Soon Kim ),김유찬 ( You-Chan Kim ),김종민 ( Jong-Min Kim ),명기범 ( Ki- 대한피부과학회 2003 대한피부과학회지 Vol.41 No.1
Background: The relative frequency and clinicopathologic characteristics of lymphomas vary according to geography and race. Data on the features of cutaneous lymphoma in Korea are limited. Objective . The aim of this study was to document the relative occ
김종우,윤영묵,김태형,김동석,김상원 ( Jong Woo Kim,Young Mook Yoon,Tae Hyung Kim,Dong Seok Kim,Sang Won Kim ) 대한피부과학회 1997 대한피부과학회지 Vol.35 No.3
We have encountered a rare case of erythema nodosum-like leukemia cutis associated with acute myelocytic leukemia(AML) in a 57-year-old male. He was in good health until about 2 weeks prior to admission, when the systemic symptoms of high fever, anorexia, general weakness and malaise, and subcutaneous nodules developed. The nodules were multiple, red and noted bilaterally on the pretibial areas. Histological findings of his skin lesions showed diffuse cellular infiltrates intermingled with leukemic cells predominantly involving the adipose tissues. The cells displayed negative stainirig to antibodies CD3 and CD20, but positive staining to LCA. The diagnosis of AML(M4) was made by blood and bone marrow studies. He had a rapid downhill course and was discharged after 2 weeks of admission, with no anti-cancer chemotherapy. (Kor J Dermatol 1997;35(3): 556 - 560)
김종우,윤영묵,김동석,김상원 ( Jong Woo Kim,Young Mook Yoon,Dong Seok Kim,Sang Won Kim ) 대한피부과학회 1997 대한피부과학회지 Vol.35 No.2
We report a case of cutaneous B cell lymphoma in a 68-year-old male who had primarily developed two 2.0 * 2.0 * 0,6cm sized, dome shaped, dark red colored tumors on the medial side of his left thigh about 4 months previously. His general condition was good and laboratory results were within normal limits, except for the enlargement of aortocaval, paraaortic and left inguinal lymph nodes. Histopathological examinations revealed diffuse dense infiltration of large atypical cells with vesicular nuclei and large prominent nucleoli in the entire dermis. They were largely composed of centroblast and immunoblast-like cells and showed positive reactions to the leukocyte common antigen, and L26 and CD22 was related to peripheral B-cell lineage in the immunohistochemical study. The skin lesions improved completely with an m-BACOD regimen. There was no relapse over a 3-year follow-up period. (Kor J Dermatol 1997;35(2): 312-316)
Atypical Polypoid Dermatofibroma
김장오 ( Jang Oh Kim ),김종우 ( Jong Woo Kim ),윤영묵 ( Young Mook Yoon ),김상원 ( Sang Won Kim ) 대한피부과학회 1996 대한피부과학회지 Vol.34 No.5
Atypical polypoid dermatofibroma(APDF) represents a distinctive clinicopathologic variant of dermatofibroma. We des~<.,ribe an unusual case of APDF occuring on the right butt~ack in a 27-year old female. The lesion was a reddish-hued, rounded, hard protuberant tumor with short pedicle, measuring 2,7 x 2.7 x 1.5cm. Excised tumor showed a well circumscribed dermal le~sion loca- lized in the protruded ar~ea, and dense proliferation of fibrobl~asts and capillaries reminiseent of fi- brous or scle~rosing hema~ngioma type, with prominent focal cellular atypia. The tumor cells were vimentin-positive, but di~rl not express CD34. There was no evidence of recurrence after 18 months postoperative foll~ow-up. (Kor J Dermatol 1996;34(5): 818-822)
Itraconazole 과 Terbinafine 투여에 저항을 보인 파종형 스포로트리쿰증 1예
김동석,김종우,김상원 대한의진균학회 1997 대한의진균학회지 Vol.2 No.2
Sporotrichosis, a deep fungal infection caused by sporothrix schenckii, is mainly treated with potassium iodide(KI) and other antifungal agents, and recently there were reports of cases treated with itraconazole or terbinafine. A 56-year-od female patient presented with multiple painless firm nodules covered with crusts measured 1.0×1.5 ㎝ and 1.0×3.0 ㎝ on the right side of neck and an crythematous plaque with ulceration measured 2.0×2.0 ㎝ on the right cheek for 20 days. Eight months before visit, she noted two subcutaneous nodules on the right side of neck. Excisional biopsy and treatment for tuberculous lymphadentitis were done. There had been no clinical prsponse for 2 months, but new painless nodulse and plaque with ulceration were developed on the opposite side of previous lesions, Biopsy showed a granulomatous change with polymorphic infiltrates, yeast cells and asteroid body. Routine laboratory findings and chest X-ray were not contributory. No evidence of tuberculosis was found in the examination with sputum and tissue. A dark brown to black., moist and wrinkled colony on the Sabouraud's dextrose agar and septate, branched mycelia and clustered conidia on slide culture were shown to be consistent with Sporothrix schenckii. Cutaneous disseminated type of sporotricosis was diagnosed. The treatment was started with 500㎎ of terbinafine daily which was known to be fungicidal, stopping of progression. The regimen was subsequently changed to intraconazole 200㎎ daily for 3 months, but new lesions were developed. So she was treated with saturated solution of potassium iodide. Five drops were given three times a day, and the dose was increased by 5 drops each day to a dose of 30 drops three times a day. Nodular lesions markedly decreased in size in two weeks, but serial tissue cultures were positive. After 3 months of administration, tissue culture was negative. No evidence of clinical relapse was noted after 3 years of follow-up.
Myxoid Liposarcoma : A Case Report
김태형,김종우,김상원,김동석,안기영 대한피부과학회 1996 Annals of Dermatology Vol.8 No.1
We report a case of well-differentiated myxoid liposarcoma in a 27-year-old female, who presented an asymptomatic, firm, deep-seated mass in the medial aspect of her left thigh. The lesion has been insidiously evolving for about one year, with a slow elevation recently over a period of several months leading to a 6.0×8.0㎝-sized mass. The regional lymph nodes were non-palpable. Histologically, the excised mass showed proliferating vimentin-positive lipoblasts in varying degree of differentiation and prominent plexiform capillary patterns, with an abundance of myxoid material in the stroma. Stage Ib was suggested by the AJC staging of the soft tissue sarcoma. She has remained free of any relapse during one-year follow-up since the wide excision of the mass.