http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
베체트병의 결절홍반모양 병변에 대한 임상 및 병리조직학적 고찰
장은주 ( Eun Joo Jang ),이지연 ( Ji Yeoun Lee ),김미경 ( Mi Kyeong Kim ),윤태영 ( Tae Young Yoon ) 대한피부과학회 2011 大韓皮膚科學會誌 Vol.49 No.6
Background: The clinical and histopathological aspects of erythema nodosum-like lesions (ELLs) in patients with Behcet`s disease (BD) may resemble those of classic erythema nodosum (EN). Although a few articles that compared ELL and EN in Korean patients have been published in the English literature, there is no comparative study between ELL and EN in the Korean dermatologic literature. Objective: The purpose of this study was to evaluate the clinical and histopathological differences between ELL and EN. Methods: We reviewed all the medical records, photographs and histopathological slides of 33 patients with ELL and 47 patients with EN at our clinic between 2000 and 2009. For all the patients, their diagnosis was confirmed based upon the clinicopathologic correlation and long term follow-up of at least more than 1 year. Results: Compared with EN, ELLs were associated with the following characteristics: a past history of inflammatory plaques and nodules (p=0.037), a relapsing course (p<0.001), dermal infiltration of neutrophils (p=0.001), mixed panniculitis (p<0.001) and subcutaneous vasculitis (p<0.001). In 6 patients (18.2%) the ELLs were the initial major symptom of BD and they didn`t have other main symptoms of BD. Compared with the patients with EN, all these patients had inflammatory plaques or nodules on other areas as well as on the lower extremities (p=0.006) and they had a relapsing course (p<0.001). In this group the mean duration of an initial major symptom to the diagnosis of BD was 16.7 months. Conclusion: Our results show that ELLs in BD can be distinguished from EN by some clinical and histopathological differences. Especially, in the patient with ELLs without other main symptoms of BD, the occurrence of lesions above the lower extremities and the relapsing course may be important clues to suspect a diagnosis of BD and to exclude a diagnosis of EN. (Korean J Dermatol 2011;49(6):499∼505)
장은주 ( Eun Joo Jang ),이동윤 ( Dong Yoon Lee ),이지연 ( Ji Yeoun Lee ),윤태영 ( Tae Young Yoon ) 대한피부과학회 2009 대한피부과학회지 Vol.47 No.11
Woolly hair is normal for most black people, but it is usually abnormal for persons of a non-African or non-Negroid background. A 5-year-old girl visited our clinic complaining of a hair abnormality. Her hair had been tightly curled, fine, and hypopigmented on the entire scalp since birth. Her uncle`s son had similar abnormalities of his scalp hairs. On the scanning electron microscopy, the patient`s hair revealed cuticular damage with splintering. To the best of our knowledge, this is the first description of a patient with woolly hair who has familial history in Korea. (Korean J Dermatol 2009;47(11):1284~1287)
과음 후 비혼수 상태의 환자에서 발생한 한선 괴사를 동반하는 수포성 병변
장은주 ( Eun Joo Jang ),이동윤 ( Dong Yoon Lee ),이지연 ( Ji Yeoun Lee ),김미경 ( Mi Kyeong Kim ),윤태영 ( Tae Young Yoon ) 대한피부과학회 2011 대한피부과학회지 Vol.49 No.11
Bullae and sweat gland necrosis is an entity previously reported to occur in comatose patients. Since its first description in comatose patients after carbon monoxide intoxication, similar lesions have also been reported in comatose patients after overdose with several drugs and in immobilized non-comatose patients. To our knowledge, there have been only three occurrences of bullae and sweat gland necrosis after alcohol intake in the Korean dermatologic literature. These cases were never described, but only summarized in a table of an original article. Herein, we more fully describe a case of bullae and sweat gland necrosis in a non-comatose patient after alcohol intake. The case demonstrates conclusively that bullae and sweat gland necrosis can occur not only in a comatose patient but also in a non-comatose patient. (Korean J Dermatol 2011;49(11):1028∼1031)
장은주 ( Eun Joo Jang ),이동윤 ( Dong Yoon Lee ),이지연 ( Ji Yeoun Lee ),김미경 ( Mi Kyeong Kim ),윤태영 ( Tae Young Yoon ) 대한피부과학회 2011 대한피부과학회지 Vol.49 No.9
Since its first description in 1887 as the appearance of psoriatic lesions in the uninvolved skin of psoriatic patients as a consequence of trauma, the Koebner phenomenon has been described in numerous diseases. Several types of injury can trigger the Koebner phenomenon, such as physical injury, surgical wound, irritation, sunburn, or radiation therapy. In this report, we describe a 43-year-old woman who developed erythema multiforme which was accompanied by the Koebner phenomenon after getting acupuncture and cupping glass therapy. The purpose of the report is to broaden our awareness of the spectrum of injury that can trigger the Koebner phenomenon. (Korean J Dermatol 2011;49(9):809~811)
겨드랑이에 발생한 다모증이 동반된 유아기 섬유성 과오종 1예
장은주 ( Eun Joo Jang ),이동윤 ( Dong Yoon Lee ),이지연 ( Ji Yeoun Lee ),윤태영 ( Tae Young Yoon ) 大韓皮膚科學會 2009 大韓皮膚科學會誌 Vol.47 No.12
Fibrous hamartoma of infancy is a rare benign lesion that presents as a solitary, painless, flesh-colored, subcutaneous mass. Most of these lesions occur in the axillary region, the upper arm, the upper trunk, the inguinal area and the external genital area. The lesion histologically consists of three different components in varying proportions: well-defined fibrous trabeculae, primitive mesenchyme and, mature adipose tissue. Overlying skin changes are uncommon, including alternations in pigmentation, eccrine gland hyperplasia and increased hair. To the best of our knowledge, only 6 cases of fibrous hamartoma of infancy with hypertrichosis have been reported. In these six cases, the lesions were located on the buttocks and back, which were non-predilection sites. We report the first case of fibrous hamartoma of infancy with hypertrichosis on the axilla, which is known as a predilection site. (Korean J Dermatol 2009;47(12):1400∼1402)
귀밑샘의 상피-근육상피암종의 세침흡인 세포소견 -2예 보고-
이혜경,장은주,김주헌,강동욱,손현진,박미자,Lee, Hye-Kyung,Jang, Eun-Joo,Kim, Joo-Heon,Kang, Dong-Wook,Son, Hyun-Jin,Park, Mee-Ja 대한세포병리학회 2008 대한세포병리학회지 Vol.19 No.2
Epithelial-myoepithelial carcinoma (EMC) is a rare low grade malignant tumor of the salivary glands and it shows a characteristic biphasic population of epithelium and myoepithelium. It shows various cytologic and histologic features, so making an exact diagnosis is difficult. We report here on two cases of epithelial-myoepithelial carcinoma arising from the parotid gland and we compare the cytologic findings of the aspirated samples with the histologic findings of the tumors. We think the finding of mixed pattern of large, clear myoepithelia and small epithelia is the most valuable finding in the diagnosis of EMC.