1.A case of hidrotic ectodermal dysplasia.
Chul Jong PARK ; Jin Wou KIM ; Si Yong KIM ; Hyung Ok KIM ; Chung Won KIM
Korean Journal of Dermatology 1991;29(6):842-845
No abstract available.
Ectodermal Dysplasia*
2.A Case of POEMS Syndrome.
Seung Churl PAIK ; Jeong Ki RHEE ; Si Yoing KIM ; Hyung Ok KIM ; Chung Won KIM
Korean Journal of Dermatology 1988;26(4):592-596
POEMS syndrome is an unusual plasma cell dyscrasia with multisystemie manifestations featuring polyneuropathy, organomegaly, endocrinopsthy, M protein and skin changes. We have seen a 49-year-old woman presenting with hyperpigmentation, hypertrichosis, hyperhidrosis, and taut thickened skin of the extremities as a skin manifestation of this syndrome. We review the literature and report a case.
Extremities
;
Female
;
Humans
;
Hyperhidrosis
;
Hyperpigmentation
;
Hypertrichosis
;
Middle Aged
;
Paraproteinemias
;
POEMS Syndrome*
;
Polyneuropathies
;
Skin
;
Skin Manifestations
3.Solitary Keratoacanthoma Developing on an Acupuncture Site.
Young Min PARK ; Si Yong KIM ; Hyung Ok KIM ; Chung Won KIM
Annals of Dermatology 1993;5(1):64-68
A 61-year-old woman, who had been treated by acupuncture on the glabellar region due to frontal headache ten days ago, had a rapidly growing tumor on that region. Histopathologically, the tumor was shown to be a central crater filled with eosinophilic keratin & a marginal but-tress formed by invagination of the epidermis. According to clinical & histopatholpgical findings, we can easily diagnose our case as solitary keratoacanthoma. As shown in our case, we think that acupuncture should be counted as one of the causative factors in the development of solitary keratoacanthoma.
Acupuncture*
;
Eosinophils
;
Epidermis
;
Female
;
Headache
;
Humans
;
Keratoacanthoma*
;
Middle Aged
4.Solitary Keratoacanthoma Developing on an Acupuncture Site.
Young Min PARK ; Si Yong KIM ; Hyung Ok KIM ; Chung Won KIM
Annals of Dermatology 1993;5(1):64-68
A 61-year-old woman, who had been treated by acupuncture on the glabellar region due to frontal headache ten days ago, had a rapidly growing tumor on that region. Histopathologically, the tumor was shown to be a central crater filled with eosinophilic keratin & a marginal but-tress formed by invagination of the epidermis. According to clinical & histopatholpgical findings, we can easily diagnose our case as solitary keratoacanthoma. As shown in our case, we think that acupuncture should be counted as one of the causative factors in the development of solitary keratoacanthoma.
Acupuncture*
;
Eosinophils
;
Epidermis
;
Female
;
Headache
;
Humans
;
Keratoacanthoma*
;
Middle Aged
5.A study on the menarche and the menstrual pattern of handicapped person.
Hyung Nam KIM ; Joong Il KIM ; Si Young JEONG ; Jae Sik SHIM ; Young Su JIN
Korean Journal of Obstetrics and Gynecology 1992;35(7):1025-1037
No abstract available.
Disabled Persons*
;
Female
;
Humans
;
Menarche*
6.Extended thymectomy in myasthenia gravis.
Kwang Jo CHO ; Hyung Ryul LEE ; Jong Won KIM ; Hwang Kiw CHUNG ; Si Chan SUNG
The Korean Journal of Thoracic and Cardiovascular Surgery 1992;25(12):1516-1522
No abstract available.
Myasthenia Gravis*
;
Thymectomy*
7.Congenital Herditary Stromal Dystrophy of the Cornea.
Si Il RYU ; Hyung Jun KIM ; Jyung Sik KWAK
Journal of the Korean Ophthalmological Society 1991;32(1):1-8
In 1978, a nonprogressive corneal dystrophy was seperated from other causes of congenital opacification on the basis of unique clinincal findings and characteristic electronmicroscopic findings. This disorder, termed congenital hereditary stromal dystrophy, appears to the result of disordered stromal fibrogenesis. Recently, the autors have experienced 4 members of a family with typical electronmicroscopic findings of congenital heaeditary stromal dystrophy of the cornea. In this report we describe the characteristic findings of congenital hereditary stromal dystrophy.
Cornea*
;
Humans
8.Circadian Variation of Ventricular Premature Complex in Hypertension and Ischemic Heart Disease Patients.
Seung Jung KIM ; Si Hoon PARK ; Gil Ja SHIN ; Woo Hyung LEE
Korean Circulation Journal 1995;25(3):581-588
BACKGROUND: Circadian rhythms have been described for acute myocardial infarction, sudden cardiac death, cerebrovascular disease, ischemic heart disease, and ventricular arrhythmia. Most of studies reported that the frequency of ventricular permature contractions(VPC's) shows a peak in day time. We tried to see that the circadian rhythm of VPC's in hypertension and ischemic heart disease(IHD) patients. And we will also studied the relationship between heart rate and frequencey of VPC's. METHOD: Twenty four hour holter monitoring was performed in hypertensive patients (N=23), ischemic heart disease patients(N=25), and normal control group(N=30). We tested the circadian pattern of VPC's and heart rates and the relationships of the frequency of VPC's and heart rates. RESULT: In hypertension group, a peak incidence of heart rate is between 5 and 8 P.M., in ischemic heart disease group, between 3 and 6 P.M.. In control group, the heart rate shows a peak beteen 1 and 3 P.M.. The frequency of VPC's in hypertension group shows the first peak between 4 and 10 P.M., and the second peak beteen 7 and 10 A.M.. In ischemic heart disease group, they show a peak between 2 and 8 P.M..In control group, there was no circadian variation for the frequency of VPC;s. Both in hypertension and IHD patients group, there was significant correlation between the frequency of VPC's and the heart rates. CONCLUSION: It seemed that VPC' were more frequently occurred in relation to the increase of heart rate in the afternoon, in hypertensive and ischemic heart disease patients.
Arrhythmias, Cardiac
;
Circadian Rhythm
;
Death, Sudden, Cardiac
;
Electrocardiography, Ambulatory
;
Heart
;
Heart Rate
;
Humans
;
Hypertension*
;
Incidence
;
Myocardial Infarction
;
Myocardial Ischemia*
;
Ventricular Premature Complexes*
9.The Differential Developmental Neurotoxicity of Valproic Acid on Anterior and Posterior Neural Induction of Human Pluripotent Stem Cells
Jeongah KIM ; Si-Hyung PARK ; Woong SUN
International Journal of Stem Cells 2025;18(1):49-58
Valproic acid (VPA), widely used as an antiepileptic drug, exhibits developmental neurotoxicity when exposure occurs during early or late pregnancy, resulting in various conditions ranging from neural tube defects to autism spectrum disorders. However, toxicity during the very early stages of neural development has not been addressed. Therefore, we investigated the effects of VPA in a model where human pluripotent stem cells differentiate into anterior or posterior neural tissues. Exposure to VPA during the induction of neural stem cells induced different developmental toxic effects in a dose-dependent manner. For instance, VPA induced cell death more profoundly during anteriorly guided neural progenitor induction, while inhibition of cell proliferation and enhanced differentiation were observed during posteriorly guided neural induction. Furthermore, acute exposure to VPA during the posterior induction step also retarded the subsequent neurulation-like tube morphogenesis process in neural organoid culture. These results suggest that VPA exposure during very early embryonic development might exhibit cytotoxicity and subsequently disrupt neural differentiation and morphogenesis processes.
10.The Differential Developmental Neurotoxicity of Valproic Acid on Anterior and Posterior Neural Induction of Human Pluripotent Stem Cells
Jeongah KIM ; Si-Hyung PARK ; Woong SUN
International Journal of Stem Cells 2025;18(1):49-58
Valproic acid (VPA), widely used as an antiepileptic drug, exhibits developmental neurotoxicity when exposure occurs during early or late pregnancy, resulting in various conditions ranging from neural tube defects to autism spectrum disorders. However, toxicity during the very early stages of neural development has not been addressed. Therefore, we investigated the effects of VPA in a model where human pluripotent stem cells differentiate into anterior or posterior neural tissues. Exposure to VPA during the induction of neural stem cells induced different developmental toxic effects in a dose-dependent manner. For instance, VPA induced cell death more profoundly during anteriorly guided neural progenitor induction, while inhibition of cell proliferation and enhanced differentiation were observed during posteriorly guided neural induction. Furthermore, acute exposure to VPA during the posterior induction step also retarded the subsequent neurulation-like tube morphogenesis process in neural organoid culture. These results suggest that VPA exposure during very early embryonic development might exhibit cytotoxicity and subsequently disrupt neural differentiation and morphogenesis processes.