1.Standard of ear size in Korean children.
Journal of the Korean Pediatric Society 1992;35(8):1089-1095
2.Clinical Observation on isolated TRH deficient Congenital Hypothyroidism.
Journal of the Korean Pediatric Society 1990;33(10):1388-1393
No abstract available.
Congenital Hypothyroidism*
3.A Case of Bleomycin induced Streaky Pigmentation and Scleroderma.
Han Gyu CHOI ; Sung Wook RO ; Myeung Nam KIM ; Chang Kwun HONG ; Byung In RO
Annals of Dermatology 1999;11(3):202-205
Bleomycin, a tumoricidal antibiotic agent, may produce unusual cutaneous manifestations such as pigmentation scleroderma, and gangrene. We report a case of the development of linear streaky pigmentation and cutaneous scleroderma in a patient treated with bleomycin for choriocarcinoma of undescented testis. The patient was 45-year-old male presented with linear brown and slate gray streaking over the trunk and extremities after three cycles of chemotherapy(bleomycin, etoposide, cisplatine). After the fourth cycle of the same chemotherapy, 18 weeks after initiation of bleomycin, the development of cutaneous scleroderma-like conditions was observed involving the same sites. Histopathologic examination showed increased basal pigmentation and thick collagen bundles through the entire dermis, extending to the subcutis. Herein, we describe a case of streaky pigmentation and scleroderma in association with bleomycin anticancer chemotherapy simultaneously in a patient.
Bleomycin*
;
Choriocarcinoma
;
Collagen
;
Dermis
;
Drug Therapy
;
Etoposide
;
Extremities
;
Female
;
Gangrene
;
Humans
;
Hyperpigmentation
;
Male
;
Middle Aged
;
Pigmentation*
;
Pregnancy
;
Testis
4.Attitudes of General University Students and Medical College Students Toward Conducting an Autopsy.
Jeong A KIM ; Gil Ro HAN ; Juck Joon HWANG
Korean Journal of Legal Medicine 1999;23(1):20-34
The attitude toward the use of autopsies affects the incidence of performance of the procedure. In foreign countries, many studies on this subjects have been conducted. However, in Korea, no study has been reported. We hypothesized that the general university students may be negative, whereas the medical college students may have positive attitude toward the use of autopsies. In contrary to our hypothesis, there existed only a little difference for the attitude toward conducting an autopsy between the general university students and the medical students. Both groups had positive attitudes toward autopsy. When the medical students become medical doctors, the main reason for not requesting patients to be conducted an autopsy is that their family members may feel offended. These results show that the low incidence of autopsy cases in Korea is caused not by the attitude of the general population, but by the attitude of medical doctors. Thus, we should make every effort to increase the incidence of autopsy by educational programs and discussions about autopsy and death.
Autopsy*
;
Humans
;
Incidence
;
Korea
;
Students, Medical
5.Growth promoting effect of recombinant methionyl-growth hormone in children with chronic renal failure.
Jeon Seok HAN ; Yong CHOI ; Hyung Ro MOON
Journal of the Korean Pediatric Society 1992;35(10):1355-1360
No abstract available.
Child*
;
Human Growth Hormone
;
Humans
;
Kidney Failure, Chronic*
6.Motherless Case in Paternity Testing.
Hye Seung LEE ; Jae Won LEE ; Gil Ro HAN ; Juck Joon HWANG
Korean Journal of Legal Medicine 1999;23(1):72-81
In parentage testing DNA profiles are used to link the alleged father with paternity by matching their patterns. The probative value of a match is often calculated by multiplying together the estimated frequencies with which each particular VNTR or STR pattern occurs in a reference population. When this calculating method applies to the motherless case of paternity disputes, a calculation must usually be based on types determined for the child and the alleged father. In such case, the first consideration is to exclude a man from paternity of a child when the man did not have the child's paternal allele at some loci, or if the paternal allele cannot be determined, when the man had neither of the child s alleles. The second is to evaluate the DNA evidence when a man is not excluded by the paternal allele. This work is to provide theories of paternity analysis with three approach methods for the motherless case, and to evaluate their efficiency compared to the trio case when the man tested is not excluded. Consequently, the motherless case offers lower probability exclusion and questionable cumulative paternity index than those of the trio case as being typed with 14 STR loci(CSF1PO, TH01, TPDX, vWA, D5S818, D13S317, D7S820, D16S539, FGA, D21S11, FES/FPS, F13A1, D18S80, D17S5). Since the motherless case in paternity disputes is less efficient for paternity exclusion of the child, the use of genetic maker systems with the higher value of mean exclusion chance(MEC) and exact levels of the relative probability of paternity must be of importance considered in the analysis of such deficiency cases.
Alleles
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Child
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Dissent and Disputes
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DNA
;
Fathers
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Humans
;
Paternity*
7.A Clinical Study of Herpes Zoster During the Last 10 Years.
Eun Sil HAN ; Heung Ryeol CHOI ; Seong Jun SEO ; Chang Kwun HONG ; Byung In RO
Korean Journal of Dermatology 1994;32(2):286-293
BACKGROUND: Herpes zoster is characterized by vesicular skin lesions over the unilateral sensory dermatomes being caused by the reactivation of varicella-zoster virus and its incidence seems to be increasing recently. OBJECTIVE: The purpose of this study was to elucidate the epidemiology and the clinical characteristics of herpes zoster. METHODS: The authors observed 877 cases of herpes zoster clinically for annual incidence, age, sex, monthly distribution, predilection site, associated disease, and complications at the Department of Dermatology in Chung-Ang University Hospital during a 10 years period(1982.9-1992.8). RESULTS: 1) The annual incidence averaged over 10 years was 2.26%(877 cases of total 38.717 outpatients) being on the increase recently. 2) The age distribution was in the range of 2-86 years old being most prevalent in the 6th decade and there was equal sex ratio(444:433). 3) There was no statistically significant monthly or seasonal variation in the incidence of herpes zoster. 4) The most common anatomical distribution was thoracic dermatome(51.7%), followed by trigeminal(17.1%), cervical(16.1%), lumbar (10.6%), sacral(1.4%)and multiple deramatomic involvement(3.1%). Left or right side was affected in about the same ratio(439:437), and bilateral involvement was in 1 case. 5) Associated disease of herpes zoster were observed in 210 patients(23.9%) ; hypertension(7.0%), diabetes mellitus(4.1%), tuberculosis(1.8%), postoperative status(0.7%), malignancy(0.7%), gastric ulcer(0.7%), and so on, 6) The most common complication of herpes zoster was postherpetic neuralgia(7.4%), followed by eye complication(2.1%), bacterial infection(1.4%), scar formation(0.7%), neurogenic bladder(0.2%), Ramsay-Hunt syndrome(0.2%), motor paralysis(0.1%), herpes zoster generalisatus(0.1%) 7) The incidence of postherpetic neuralgia increased with age and was highest in trigeminal dermatome. 8) Recurrence of herpes zoster was observed in 4 patients(0.5%). CONCLUSION: According to this study, the annual incidence of herpes zoster showed a tendency to increase recently but there was no significant monthly or seasonal variation. The anatomical distribution was most commom on the thoracic dermatome. The incidenc of postherpetic neuralgia increased with age being most common in trigeminal nerve.
Age Distribution
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Cicatrix
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Dermatology
;
Epidemiology
;
Herpes Zoster*
;
Herpesvirus 3, Human
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Incidence
;
Neuralgia, Postherpetic
;
Recurrence
;
Seasons
;
Skin
;
Trigeminal Nerve
8.Angiofollicular Lymph Node Hyperplasia(Castleman's disease): 3 cases report.
Jeong Hee PARK ; Gil Ro HAN ; Hee Jin CHANG ; Jin Hee SOHN ; Jung Il SUH
Korean Journal of Pathology 1992;26(3):298-305
Angiofollicular lymph node hyperplasia(AFLNH) was first described in 1956 by Castleman et al. It was initially reported as a solitary mediastinal mass but multicentric and extranodal disease is now well known. Histologically two distinct variants, e.g. the hyaline vascular type and the plasma cell type, of AFLNH are recognized. And the plasma cell type is typically associated with clinical syndrome consisting of fever, anemia, elevated erythrocyte sedimentation rate and polyclonal hypergammaglobulinemia. Recently, we experineced three cases of AFLNH. Histologically, two cases were hyaline vascular type, that were presented as a right supraclavicular mass of 49-year-old female, and as an anterior mediastinal mass of 53-year-old female. The remaining one case was plasma cell type that was presented as a left axillary mass of 63-year-old male. The former two cases showed typical features of hyaline vascular type but in case 1, exuberant proliferation of hyalinized vessels of capillary size was characteristic feature. The latter case of plasma cell type characteristically showed clinical syndrome consisting of fever, hypoalbuminemia, polyclonal hypergammaglobulinemia. All cases were presented as a single mass and they were well after surgical excision.
Female
;
Humans
9.Two Case of Watson-Alagille Syndrome.
Heon Seok HAN ; Soo Heum LIM ; Young Sun KIM ; Jeong Kee SEO ; Hyung Ro MOON
Journal of the Korean Pediatric Society 1985;28(10):1047-1051
No abstract available.
10.A Clinical Study of Androgenetic Alopecia.
Eun Sil HAN ; Myeung Nam KIM ; Chang Kwun HONG ; Byung In RO
Korean Journal of Dermatology 1995;33(1):44-52
BACKGROUND: Androgenetic alopecia is considered to be a genetically determined disorder influenced by age and androgen. The proportion of patients with androgenetic alopecia among the total number of patients with alpecia seems to be gradually increasing. OBJECTIVE: The purpose of this study is to determine the family history, clinical and endocrine status of the patients with androgenetic alopectia. METHODS: 387 patients with androgenetic alopecia who had visited the Department of Dermatology, Yongsan Hospital, College of Medicine, Chung-Ang University during the last 4 years (1990.1-1993.12)were examined. RESULTS: 1) Annual incidence of androgenetic alopecia among the total number of alopecia patients averaged over 4 years was 38.95 having increased recently. 2) There were 286 male and 101 female patients being most prevalent in the 3rd decade in both sexes. 3) Patients younger than 30 years old, patients with premature androgenetic alopecia, made up 687.5% of the male patients and 56.4 of the female patients with androgenetic alopecia. 4) Of the 73 male patients Hamilton's type III was most common (46, 63.0%). 5) Of the 34 female patients Ludwig's type I was most common (21, 61.2%). 6) there was a family history of baldness in 39.4% of first degree relatives in male patients and 41.25 of first degree relatives in female patients. 7) Associated diseases were observed in 152 (53.1%) of the male patients and 63(62.4%) of the female patients : seborrheic dermatitis (36.7%/35.7%), acne vulgaris (5.2%/5.95), atopic dermatitis, thyroid diseases, pulmonary tuberculosis, depression, and gastrointestinal diseases. In female patients menstrual irregularity, hypertrichosis, and polycystic ovary disease were also observed. 8) Serum testosterone levels were increased in 24 (8.8%0 of male patients and in 17 (17.45) of female patients. CONCLUSION: Based on our findings, the development of androgenetic alopecia is significantly related to the positive family history of baldness. Serum testosterone levels in most patients were within normal limit and were increased only in a small number of the patients with androgenetic alopecia. Therefore, it seems reasonable to suggest that the inhibitory effecfts of androgens on the dermal papilla cells may be mediated by an increased density and/or functional activity of androgen receptors or through an acceleration in the metabolic activity of androgen.
Acceleration
;
Acne Vulgaris
;
Adult
;
Alopecia*
;
Androgens
;
Depression
;
Dermatitis
;
Dermatitis, Atopic
;
Dermatitis, Seborrheic
;
Dermatology
;
Female
;
Gastrointestinal Diseases
;
Humans
;
Hypertrichosis
;
Incidence
;
Male
;
Ovary
;
Receptors, Androgen
;
Testosterone
;
Thyroid Diseases
;
Tuberculosis, Pulmonary