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김용준 ( Yong Joon Kim ),김명남 ( Myeung Nam Kim ),홍창권 ( Chang Kwun Hong ),송계용 ( Kye Yong Song ),노병인 ( Byung In Ro ) 대한피부과학회 1996 대한피부과학회지 Vol.34 No.5
Microcystic adnexal c~arcinoma(MAC) is an unusual carcinoma of eccrine glands, composed of pilar and: weat. duct structures. We report here a 64-year-old man with MAC on his left cutaneous upper lip. Microscopically, the tumor consisted of nests and gland-like str~i~ictures within desmoplastic stroma, and it stained positively for carcinoembryonic antigen. The clinical appearance and histopathologic findings of t,he tumor may be mistaken for other benign and malignant entities. The patient was treated with excision and skin flap, and no recurrence over a 31-month follow up period. (Kor J Dermatol 1996;34(5): 823-826)
김용준 ( Yong Joon Kim ),서성준 ( Seong Jun Seo ),김명남 ( Myeung Nam Kim ),홍창권 ( Chang Kwun Hong ),송계용 ( Kye Yong Song ),노병인 ( Byung In Ro ) 대한피부과학회 1996 대한피부과학회지 Vol.34 No.5
Background: Dermatofihromas are relatively common benign tumors which occur in the skin. However, clinical and histopathological studies have been rarely reported in Korea. Objective : This study was taken to evaluate the clinical and histopathological features of dermatofibromas in Korea. Methods : Fifty cases of dermatofibromas were selected from 10 years of laboratory files for during the period January 1985 to December 1994 at Chung Ang University Hospitals. Results : 1. The age range was from 18 to 61 and the average age at diagnosis was 38.7(male;37.6, female;39.4). The ratio of male to female was 1.0: 1.6(19:31). 2. The diameter of the dermatofibromas : 1) 5-20mm;32 cases(64.0%), 2) 5mm>;8 cases(16.0 %), 3) 20mm<;7 cases(14.0%), 4) unrecorded;3 cases(6.0%). 3. The most common color was brown(14 cases, 28.0% ), and other common colors were skin-color(7 cases, 14.0%), red(4 cases, 8.0%), black(3 cases, 6.0%), violaceous(2 cases, 4.0%), unknown(20 cases, 40.0%). 4. Thirty seven cases(74.0%) had solitary lesions, and thirteen cases(26.0%) had multiple lesions. 5. The lower extremeties(39 cases, 50.6%) were the most common sites followed by the back (10 cases, 13.0%), upper extremities(9 cases, 11.7%), shoulders(8 cases, 10.4%), abdomen(4 cases, 5.2%), hands(2cases, 2.6%), face(2 cases, 2.6%), neck(2 cases, 2.6%), breast(1 case, 1.3%). 6. Histopathologically, fibrous types were seen in 40 cases(80.0%), cellular types in 3 cases(6.0 %), mixed types in 5 cases(10.0%), and sclerosing hemangiomas in 2 cases(4.0%). Conclusion : The 50 cases of dermatofibromas, which were confirmed at Chung Ang University Hospitals from January 1985 to December 1994, were reviewed clinically and histopathologically. (Kor J Dermatol 1996;34(5): 769-774)
김범준 ( Beom Joon Kim ),김유진 ( Yu Jin Kim ),김명남 ( Myeung Nam Kim ),노병인 ( Byung In Ro ),송계용 ( Kye Yong Song ) 대한피부과학회 2002 대한피부과학회지 Vol.40 No.12
The nenrofibromatoses are a heterogenous set of genetic disorders having clinical manifestations that involve the skin, the nervous system, or both. Vitiligo is a pigmentary disorder in which acquired destruction of melanocytes causes depigmented patches of various shapes and sizes. Although the cause is unknown, various theories such as the autoimmune, autocytotoxic, and neural hypotheses have been proposed. We report two cases of neurofibromatosis with vitiligo in the same patients, which is the nut report of concurrence of type I neurofibromatosis and vitiligo. (Korean J Dermatol 2002;40(12) : 1561∼1565)
노용관 ( Yong Kwan Rho ),김범준 ( Beom Joon Kim ),김명남 ( Myeung Nam Kim ),노병인 ( Byung In Ro ) 대한피부과학회 2008 대한피부과학회지 Vol.46 No.6
Background: Androgenetic alopecia is the most common form of hair loss in people with a genetic predisposition. It is characterized by the miniaturization of terminal hair follicles and the formation of vellus-like follicles. Objective: The aim of this study was to evaluate the prevalence, clinical manifestation, genetic and endocrine factor, and associated diseases of Korean patients with androgenetic alopecia. Methods: We studied 789 Korean men and women with androgenetic alopecia. A detailed history was taken and their hormonal values were measured. A pelvic ultrasound scan was performed to check for abnormalities the ovaries and uterus of 56 women with androgenetic alopecia. Results: The number of men was 1.9 times more (520) than that of women (269). Most of them were in their twenties (male 223; 42.8%, female 85; 31.5%). In the 520 male patients, Norwood class IIIv was dominant (161 patients; 30.9%). In the 269 female patients, Ludwig class I was superior (218 patients; 81%). 395 (75.9%) of male patients and 198 (73.6%) of female patients had a family history of androgenetic alopecia. The most common associated disorder was seborrheic dermatitis (male 407; 78.2%, female 155; 57.6%). And others included atopic dermatitis, hypertension, thyroid disease, etc. Serum testosterone levels were increased in 92 (17.6%) of the male patients and in 36 (13.3%) of the female patients. Abnormal pelvic ultrasound findings were observed in 10 (18%) of 56 female patients, and the conditions were ovarian cysts (8.9%), Uterine myoma (5.4%), uterine mass (2%), endometrial mass (2%). Conclusion: Androgenetic alopecia is a disease that has genetic and familial tendency and is associated with the androgen level. The number of androgenetic alopecia patients was increasing and type IIIv was most common in the male patients. The pelvic ultrasound showed an increased rate of abnormal findings in the female patients with androgenetic alopecia, but ultrasound is not an appropriate routine test to evaluate. (Korean J Dermatol 2008;46(6):729∼735)
강성준(Seong Joon Kang),노병선(Byoung Seon Rhoe),김수용(soo Yong Kim),이연희(Yeon Hee Lee),이창일(Chang Il Lee) 대한소화기학회 1993 대한소화기학회지 Vol.25 No.1
N/A Despite the support provided by adjuncts such as total parenteral nutrition, effective antibiotic. and hemodynamic monitoring, esophageal perforations continue to be associated with a mortality rate of more than 20%. In an effort to refine and improve treatment, we reviewed 6 cases of esophageal perforations from January, 1983 to August, 1992. The prevalent age group was 4th to 6th decades. The perforation site was cervical (2), thoracic (1) and distal (3). Clinical findings were fever, pain, dysphagia, and subcutaneous emphysema in cervical esophageal perforations compared with chest pain and epigastric pain in thoracic or distal esnphageal perforations. Causes of esophageal perforation were trauma, 2 cases, in cervical region and spontaneous rupture (Boerhaave syndrome), 4 cases in thoracic and distal region. Preoperatively, we performed simple neck and chest X-ray, esophagoscopy, fiberoptic gastroscopy (FGS) and esophagogram. Mortality was developed in 2 cases (33.3%p) and its causes were sepsis due to mediastinitis with delayed aclmission. In operative management, we recommed primary repair and drainage in cervical esophageal perforation. But in thoracic and distal esophageal perforation, the repair site should be butressed with viable serosal butress such as pleura and pericardium, if possible, to prevent subsequent leak at the suture line. 1n conclusion, early diagnosis and early operation is easential for patients with spill of contrast medium on esophagograms of clinical manifestations of esophageal soilage of the mediastinum or pleural cavities.
김용준,서성준,홍창권,노병인 ( Yong Joon Kim,Seong Jun Seo,Chang Kwun Hong,Byung In Ro ) 대한피부과학회 1997 대한피부과학회지 Vol.35 No.1
A 62 year old man had skin eruptions, general weakness, swallowing difficulty, and fever for 3 months. Diagnosis of dermatomyositis was established on the bases of clinical manifestations, muscle enzyrne study, electromyogram and histopathological findings of skin and muscle. Borrman type g stomach cancer was found by gastroendoscopy and computed tomography. He refused surgical operation for stomach cancer and died 2 months later. (Kor J Dermatol 1997;35(l): 174-178)
조백기,박종갑,김형옥,김성욱,백승철,김진우,김시용,안규중,전재복,오지원,김낙인,이규석,오칠환,김수남,김상태,손숙자,신용우,김동석,이원우,권경술,서대헌,황규왕,이종석,고재경,강원형,정기양,최응호,김기홍,박석돈,강승주,함정희,명기범,김방순,구상완,김병수,원영호,김한욱,송은섭,정병수,노병인,홍창권,박장규,한지윤,김광중,구대원,김종민,김재홍,유희준,양경미 대한의진균학회 1998 대한의진균학회지 Vol.3 No.2
Background: Onychomycosis, especially toenail onychomycosis has become one of the common fungal infection and has historically been regarded as a cosmetic rather than medical problem by many patients, even by physicians. Recently, however, there are several reports that is a refractory disease which may cause a deleterious effect on patiets quality of life (QOL). Objective: The purpose of this study was to investigate the impact of toenail onychomycosis on QOL in Korea and to assess the chandes of QOL after treatment. Methods: Total 1004 patients with toenail onychomycosis which was confirmed by clinical findings and KOH preparation were were enrolled at 47 dermatologic centers in Korea, and interviewed with standardized QOL questionnaire before and after sytemic antifungal treatment. Responses to the questionnaire were scored by 5-point scale (1∼4) and averaged, and were analyzed for 5 dimensions of emotional impact, social impact, symptorn and functional impact, patients views concerning treatment, and relationship with doctor. Results: 1. Before and after treatment, the most serious impact was emotional dimension showing 1.90 and 1.30 in average score (AS), and social (AS: 1.14 and 0.83) and symptom and functional impact (AS: 1.05 and 0.92) was also affected. 2. In female rather than male, statistically more significant impact on patients QOL was observed in all dimensions. 3. After treatment, 3 of 5 dimensions were improved significantly - emotional dimension (AS : from 1.90 to 1.30), social dimension (AS: from 1.14 to 0.83), patients view concerning treatment (AS: from 1.34 to 1.02). 4. The drgree of patients satisfaction at the therapeutic effect was very high- 62.4% (immediately after treatment) and 65.8% (9 months affer initiation of treatment) of patients answered excellent or good. Conclusion: This study confirms that toenail onychomycosis has significant impact on the overall QOL of patients. Also the effect of antifungal therapy on patients QOL were watisfactory. Therefore, both doctor and patient should pay more attention to the treatment of onychomycosis. [Kor J Med Mycol 3(1): 115∼124]
김범준,정유선,김명남,노병인,송계용 대한피부과학회 2002 大韓皮膚科學會誌 Vol.40 No.10
Dermatomyositis is a rare inflammatory myopathy with characteristic skin manifestations and muscular weakness. Immunologic factors are most likely involved in the pathogenesis of the disease. We describe a 44 year old man with a 5 month history of severe pruritus on the trunk and upper extremities with intermittent tremor of upper extremities. Hydroxychloroquine and methotrexate were combined with glucocorticoids for one month, improvement of clinical manifestations could be observed.