1.A case of mucocele of the sphenoid sinus causing complete visual loss.
Young Min KIM ; Young Min PARK ; Young Cho KOH
Korean Journal of Otolaryngology - Head and Neck Surgery 1992;35(4):590-595
No abstract available.
Mucocele*
;
Sphenoid Sinus*
2.DNA ploidy of gastric cancer and it's adjacent mucosa.
Dong Yi KIM ; Chol Gyoon CHO ; Young Kook CHO
Journal of the Korean Cancer Association 1992;24(2):227-232
No abstract available.
DNA*
;
Mucous Membrane*
;
Ploidies*
;
Stomach Neoplasms*
3.A Case of Lupus Vulgaris Developed on the Glasn Penis.
Young Pio KIM ; Jil Heyeun CHO
Korean Journal of Dermatology 1976;14(3):247-253
A 36-year-old rnarried man showed an irregularly shaped, brownish red, relatively well dernarcated and not indurated. ulcer margin with moderately uneven yellowish base on his glan penis, which had begun as erythematous macules ahout 4 nonths prior to consultation. No discomfort was associated with the ulcer. With the aid of clinicopthological a.nd histopathological studies, the authors diagnosed this skin disease as Lupus Vulgaris. Both the literature and clinical obserbation identify the face as the site of predilection for Lupus Vulgaris. Because of this patient's remarkable site of presentation, a review of the litrature is presented along with the case report.
Adult
;
Humans
;
Lupus Vulgaris*
;
Male
;
Penis*
;
Skin Diseases
;
Ulcer
4.The metastatic features in the colorectal cancer.
Journal of the Korean Surgical Society 1992;42(5):643-649
No abstract available.
Colorectal Neoplasms*
5.A comparative study on the efficacy of low-dose intradermal hepatitis B vaccination.
Journal of the Korean Academy of Family Medicine 1992;13(1):28-34
No abstract available.
Hepatitis B*
;
Hepatitis*
;
Vaccination*
6.Genetic Observation of Familial Benign Chronic Pemphigus ( Hailey - Hailey Disease ) and Report of Two Cases with Review of Literatures.
Young Pio KIM ; Jill Heyeun CHO
Korean Journal of Dermatology 1975;13(1):61-68
Familial Benign Chronlc Pemphigus (Hailey-Hailey disease) is relatively rare, persistent, recurrent vesiculo-bullous and inheritable dermatitis. Forty-nine and twenty four year-old two Korean men,affecting classical form of Hailey-Hailey disease, manifested circinated or configurated form of impetiginous, vesiculo-bullous, crusted and pigmented skin lesions over the axillae, neck, shoulder, lower abdornen, inguinal, inner aspect of upper portion of thigh, genito-crural and popliteal space of the skin, There were seen also actively inflammatory border that spread peripherally producing circinate and configurate patterns, and found satellite lesions resembling cutaneous candidiasis in some areas of the lesion. However, eye lesion or lymphnode swelling was not found. Nikolsky sign was present in both patients. The patients had pruritus, intense or slight, over the lesion. The onset of the disease in the cases was mid-twenty and early twenty, and the durations were over twenty years and three years, respectively, and genetic observation on the families revealed that four persons in the two generations and eight persons in the four generations were affected, respectively, and ratio of male to female affected were 5: 1. Routine laboratory examinations including bacteriological and mycological studies revealed non-specific findings. Histopathologic studies showed acantholytic and individual cells in the intra-epidermal bulla, and lacunae, villi, single basal cell lined papillae appearing at the bottom of the bulla, and so-called "dilapidated brick wall" appearance to be seen at the top of blula. Authors discussed the gentic pattern of Familial Benign Chronic Pemphigus (Hailey-Hailey disease) in the two families and presented two cases of the disease with laboratory examinations, histopathological findings and clinical symptoms of the patients, and confirmed that the disease is transmitted as "irregular autosomal dominant" trait, and stressed the difference in frequency, of the diseae according to sex, I.e., in male were more prevalent than female, and reviewed the related literatures af the disease.
Axilla
;
Candidiasis, Cutaneous
;
Dermatitis
;
Family Characteristics
;
Female
;
Humans
;
Male
;
Neck
;
Pemphigus
;
Pemphigus, Benign Familial*
;
Pruritus
;
Shoulder
;
Skin
;
Thigh
7.Genetic Observation of Familial Benign Chronic Pemphigus ( Hailey - Hailey Disease ) and Report of Two Cases with Review of Literatures.
Young Pio KIM ; Jill Heyeun CHO
Korean Journal of Dermatology 1975;13(1):61-68
Familial Benign Chronlc Pemphigus (Hailey-Hailey disease) is relatively rare, persistent, recurrent vesiculo-bullous and inheritable dermatitis. Forty-nine and twenty four year-old two Korean men,affecting classical form of Hailey-Hailey disease, manifested circinated or configurated form of impetiginous, vesiculo-bullous, crusted and pigmented skin lesions over the axillae, neck, shoulder, lower abdornen, inguinal, inner aspect of upper portion of thigh, genito-crural and popliteal space of the skin, There were seen also actively inflammatory border that spread peripherally producing circinate and configurate patterns, and found satellite lesions resembling cutaneous candidiasis in some areas of the lesion. However, eye lesion or lymphnode swelling was not found. Nikolsky sign was present in both patients. The patients had pruritus, intense or slight, over the lesion. The onset of the disease in the cases was mid-twenty and early twenty, and the durations were over twenty years and three years, respectively, and genetic observation on the families revealed that four persons in the two generations and eight persons in the four generations were affected, respectively, and ratio of male to female affected were 5: 1. Routine laboratory examinations including bacteriological and mycological studies revealed non-specific findings. Histopathologic studies showed acantholytic and individual cells in the intra-epidermal bulla, and lacunae, villi, single basal cell lined papillae appearing at the bottom of the bulla, and so-called "dilapidated brick wall" appearance to be seen at the top of blula. Authors discussed the gentic pattern of Familial Benign Chronic Pemphigus (Hailey-Hailey disease) in the two families and presented two cases of the disease with laboratory examinations, histopathological findings and clinical symptoms of the patients, and confirmed that the disease is transmitted as "irregular autosomal dominant" trait, and stressed the difference in frequency, of the diseae according to sex, I.e., in male were more prevalent than female, and reviewed the related literatures af the disease.
Axilla
;
Candidiasis, Cutaneous
;
Dermatitis
;
Family Characteristics
;
Female
;
Humans
;
Male
;
Neck
;
Pemphigus
;
Pemphigus, Benign Familial*
;
Pruritus
;
Shoulder
;
Skin
;
Thigh
8.Isolation of Echovirus Serotype 25 from Patient with Hand , Foot and Mouth Disease in Pusan , 1998.
Young Hee KIM ; Kyung Soon CHO
Journal of the Korean Society for Microbiology 1999;34(2):157-162
Identification of virus is very importnant in aspects of preventive surveillance system of viral infection. The first isolation of echovirus serotype 25 from hand, foot and mouth disease was accomplished in Pusan, 1998. The authors determined some properties of this virus. Two cases of outbreak were confirmed from the stools of a 3 year-old girl and one 4 year-old boy suffering from hand, foot and mouth disease. Both occurred in April. The isolated viruses showed strong cytopathic effect on RD cells, also on HEp-2, and Vero cell lines after 3 days at 34'C, CO incubation. Isolated virus was identified as echovirus serotype 25 by neutralizing antibody test. Electron micrograph of negative-stained echovirus serotype 25 showed non-enveloped, isometric particle and about 30 nm in diameter.
Animals
;
Antibodies, Neutralizing
;
Busan*
;
Child, Preschool
;
Enterovirus B, Human*
;
Female
;
Foot*
;
Foot-and-Mouth Disease*
;
Hand*
;
Hand, Foot and Mouth Disease
;
Humans
;
Male
;
Vero Cells
10.Study of motor development in cerebral palsy.
Journal of the Korean Academy of Rehabilitation Medicine 1991;15(3):334-341
No abstract available.
Cerebral Palsy*