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Case Report : Localized Sweet`s Syndrome in an Irradiated Field
Ga Youn Lee,Mi Ok Do,Seong Hyun Kim,Hae Young Choi,Ki Bum Myung,You Won Choi 대한피부과학회 2009 Annals of Dermatology Vol.21 No.3
Sweet`s syndrome is a reactive dermatosis characterized clinically by fever, leukocytosis, and multiple, erythematous, painful plaques. Histopathologic examination reveals a band-like dense dermal inflammatory infiltrate composed mainly of neutrophils with papillary dermal edema, and no features of vasculitis. We report a case of a 56-year-old female diagnosed with cervical cancer, who underwent surgery and concurrent chemoradiation therapy. Approximately 3 years after completing treatment, she presented with erythematous plaques, principally within the radiation field; the skin biopsy showed features consistent with Sweet`s syndrome. (Ann Dermatol 21(3) 300~303, 2009)
이가연 ( Ga Youn Lee ),최유원 ( You Won Choi ),명기범 ( Ki Bum Myung ),최혜영 ( Hae Young Choi ) 대한피부과학회 2009 대한피부과학회지 Vol.47 No.7
Eccrine syringofibroadenoma (ESFA) is a rare, benign adnexal neoplasm of eccrine ductal differentiation. It shows variable clinical findings ranging from a solitary papule or nodule to multiple lesions withlinear or diffuse distribution. Typically, it occurs as a solitary nodule on the extremities of elderly people. Histopathologic findings usually show proliferation of anastomosing cords and strands of cuboidal epithelial cells embedded in fibrovascular stroma. We report an uncommon case of solitary eccrine syringofibroadenoma with plasma cell infiltration on the dorsum of the foot of a 53-year-old man. (Korean J Dermatol 2009;47(7):846~849)
이가연 ( Ga Youn Lee ),한유진 ( You Jin Han ),최유원 ( You Won Choi ),명기범 ( Ki Bum Myung ),최혜영 ( Hae Young Choi ) 대한피부과학회 2010 大韓皮膚科學會誌 Vol.48 No.7
We report here on a 63-year-old woman who presented with recurrent bruise-like infiltrative plaques on the left leg without systemic symptoms or laboratory abnormalities. The histopathologic findings showed an infiltration of panniculus by small to medium-sized atypical lymphocytes. But the prominent lymphoid atypia, fat necrosis, vascular thrombosis, erythrophagocytosis and striking dominance of CD8+lymphocytes seen in subcutaneous panniculitis-like T-cell lymphoma (SPTCL) were not detected. The diagnosis of atypical lymphocytic lobular panniculitis (ALLP) was made based on these histopathologic and clinical features. The lesions responded well to systemic steroid treatment. But the CD4/CD8 ratio in the later lesion was more decreased than that of the initial lesion, and the patient is under clinical follow up. (Korean J Dermatol 2010;48(7):637∼641)
이현주 ( Heun Joo Lee ),이승재 ( Seung Jae Lee ),박지혜 ( Ji Hye Park ),최종원 ( Chong Won Choi ),이가영 ( Ga Young Lee ),김원석 ( Won Serk Kim ),윤상웅 ( Sang Woong Youn ) 대한피부과학회 2013 대한피부과학회지 Vol.51 No.3
Sarcoidosis is a multisystem disorder. Among various morphologies of cutaneous sarcoidosis, micropapular sarcoidosis is a rare form of cutaneous sarcoidosis. Clinically, the syndrome presents with the micropapules on the skin. Micropapular sarcoidosis involves the eyes frequently, while lung involvement is not common. Herein, we report a case of micropapular cutaneous sarcoidosis with ocular involvement. A 35-year-old Korean woman, with a history of uveitis and glaucoma, presented with progressive, tiny papular skin lesions. The histologic findings showed granulomatous inflammation composed of epithelioid granulomas in the upper dermis. The chest computed tomography showed no abnormalities. The patient in this case was diagnosed as having micropapular sarcoidosis and was treated with oral prednisolone. (Korean J Dermatol 2013;51(3):199∼201)