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서성준(Seong Jun Seo),홍창권(Chang Kwun Hong),송계용(Kye Yong Song),김범준(Beom Joon Kim),김유진(Yu Jin Kim) 대한피부과학회 2002 대한피부과학회지 Vol.40 No.9
Relapsing polychondritis is a rare systemic disorder manifested by recurring episodes of inflammation in cartilagenous tissues including the eye, the audiovascular systems, We describe a 53-year-old oriental woman with a one month history of painful swelling of both accompanied by intermittent hoarseness, dyspnea, impaired visual acuity, and swelling of hands. Both ear were typically uninvolved. Auricle including cartilaginous tissues were histologically examined, which revea1ed loss of basophilic staining, degenerative changes, inflammatory cells infiltrations with eosinophils and neutrophils, and perichon4rial inflammation of the cartilage. Oral prednisolone and colchicine were prescribed and the succid resolulion of both ears swelling were observed. As the disease progressed optic neuritis and chewing difficu1ty by non-erosive motion limit of temporo-mandibular joints developed, (Korean J Dermatol 2002;40(9) : 1111~1115)
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)
김범준(Beom Joon Kim),서성준(Seong Jun Seo),송계용(Kye Yong Song),홍창권(Chang Kwun Hong) 대한피부과학회 2002 대한피부과학회지 Vol.40 No.6
Cheilitis granulomatosa is a rare disorder of uncertain etiology and characterized by a recurrent orofacial swelling, which was described by Miescher in 1945 lot the first time. Symptoms usually manifest during adolescence and initially transient, but subsequently a chronic progressive disability develops. No efficient mode of therapy is yet available. A 71-year-old woman presented with a prominent upper lip swelling which had persisted for more than 6 years. There were no fissuring of the tongue and facial palsy. Oral prednisone was instituted for 6 months with moderate clinical improvement. 2 years later, multiple biopsies we, performed at the hard palate, gingiva. and inferior turbinate. And the specimens from the gingiva and inferior turbinate showed scattered non-caseating granulomas, consistent with `Cheilitis Granulomatosa.` We present here our experience with long-term trial of oral corticosteroid in a 71-year-old woman with cheilitis granulomatosa who had suffered recurrent labial swelling.
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)
홍지연 ( Ji Yeon Hong ),서준혁 ( Joon Hyuk Suh ),이갑석 ( Kapsok Li ),서성준 ( Seong Jun Seo ) 대한피부과학회 2018 대한피부과학회지 Vol.56 No.7
Focal acral hyperkeratosis (FAH) is a rare genodermatosis inherited by autosomal dominant transmission; however, some sporadic cases have also been reported. FAH is characterized by multiple late-onset crateriform hyperkeratotic papules with a yellow color on the border of the hands and feet. A 31-year-old man presented with yellowish discrete flat-topped papules on the lateral side of his palms and fingers. The patient had a family history of similar lesions throughout three generations. The histological findings revealed hyperkeratosis with mild hypergranulosis in the epidermis, and the dermis showed no specific changes including elastorrhexis. These clinicopathologic findings were consistent with the diagnosis of FAH. Herein, we report a rare case of FAH with autosomal dominant inheritance. (Korean J Dermatol 2018;56(7):443∼446)
노용관 ( Yong Kwan Rho ),유광호 ( Kwang Ho Yoo ),김지영 ( Ji Young Kim ),이갑석 ( Kap Sok Li ),서성준 ( Seong Joon Seo ),홍창권 ( Chang Kwun Hong ),송계용 ( Kye Yong Song ) 대한피부과학회 2009 대한피부과학회지 Vol.47 No.1
Epidermal nevi are harmatormas that are the result of developmental malformations of the epidermis, and these lesions present with a variety of clinical and histological characteristics. Some tumors can arise in epidermal nevi because epidermal nevi develop from multipotent germinative cells. We report here on a 57-year-old woman who had epidermal nevi arranged in a linear pattern since childhood. Her epidermal nevi were located in her left chest, arm and shoulder, upon which multiple trichillemal cysts seemed to develop after several years. We think that this patient with linear epidermal nevi associated with multiple trichilemmal cysts is a rare and distinctive case. (Korean J Dermatol 2009;47(1):55~58)
오인영 ( In Young Oh ),김현규 ( Hyun Kyu Kim ),박귀영 ( Kui Young Park ),이갑석 ( Kap Sok Li ),김범준 ( Beom Joon Kim ),서성준 ( Seong Jun Seo ),김명남 ( Myeung Nam Kim ),홍창권 ( Chang Kwun Hong ) 대한피부과학회 2012 대한피부과학회지 Vol.50 No.7
Syphilis, the great imitator of skin diseases, is a chronic systemic infectious disease with a waxing and waning course. Clinical manifestations of syphilis are variable in appearance and have been described for centuries. Especially, secondary syphilis is characterized by large diversity of presentation. They include macular, papular, papulosquamous, syphilis cornee, psoriasiform, annular en cockade, nodular, condylomata lata, malignant syphilis, mucosal lesions, loss of the hairs, and alteration of the nails. Nail involvement of syphilis includes changes on nail plate (syphilitic onychia) or periungual tissue (syphilitic paronychia). A 20-year-old man was presented with multiple erythematous broad eroded surfaced papules and macules on the scrotum and scaly exfoliated patch with erythematous swelling on the right thumb with onychodystrophy and mild tenderness on the nail. Serological screening for syphilis showed increased titer for VDRL (1:16) and TPHA (+). After intramuscular treatments with benzathine penicillin G, the skin lesions on the scrotum cleared within 1 month and the nail dystrophy showed slight improvement. (Korean J Dermatol 2012;50(7):628∼631)
유광호 ( Kwang Ho Yoo ),노용관 ( Yong Kwan Rho ),김동하 ( Dong Ha Kim ),박주희 ( Ju Hee Park ),김범준 ( Beom Joon Kim ),김명남 ( Myeung Nam Kim ),한태영 ( Tae Young Han ),이갑석 ( Kap Sok Li ),서성준 ( Seong Jun Seo ),홍창권 ( Cha 대한피부과학회 2009 대한피부과학회지 Vol.47 No.7
Background: Androgenic alopecia (AGA) is characterized by the local and gradual transformation of terminal scalp hair into vellus hair, which has a shorter and thinner shaft. It is the most common form of hair loss in people with a genetic predisposition for baldness. Objective: The aim of this study was to evaluate the prevalence, AGA type, family history, co-morbidity diseases, stress factors and endocrine factors of AGA patients. Methods: We examined a total of 432 male and female AGA patients who visited for two years at the Department of Dermatology, School of Medicine, Chung-Ang University. Results: There were 2.06 times more men (291 patients) than women (141 patients) among the study subjects. Most of the men were in their twenties (108, 37.1%), however, most of the women were in their forties (42, 29.7%). In the 291 male patients, Norwood class IIIv was dominant (120 patients, 41.2%). In the 141 female patients, Ludwig class I was dominant (87 patients, 61.7%). 219 (75.2%) of the 291 male patients and 81 (73.6%) of the 141 female patients had a family history of AGA. 224 (76.9%) of the 291 male patients and 101 (53.4%) of the 141 female patients had a co-morbidity disorder. The most common among these disorders in both the male and female patients was seborrheic dermatitis. Stress factors were observed in 162 (55.6%) of the 291 male patients and in 78 (55.3%) of the 141 female patients. The most common stress factor in both the male and female patients was work tasks. The serum testosterone levels was increased in 51 (17.5%) of the 291 male patients and in 20 (14.1%) of the 141 female patients. Conclusion: Most of the study results are compatible with those of our previous study. Yet the following results were different: (1) the number of female AGA patients in their forties is increasing; and (2) stress was found to be associated with AGA in both the male and female patients. (Korean J Dermatol 2009;47(7):765~771)