1.Comparison of Techniques for Correcting the Prominent Ear in Rabbits.
Jin Soo KO ; Seung Han KIM ; Seung Hong KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1999;26(5):1035-1039
The relative merits of cartilage scoring versus suturing in techniques for correcting the prominent ear remains a subject of debate among leading plastic surgeons. We compared a variety of echniques for correcting the prominent ear in 72 rabbit ears using scoring, horizontal mattress sutures, and combination scoring and suturing. The ears were splinted with a right-angle fold for 3 postoperative weeks, and the animals were sacrificed after 8 weeks. Suturing techniques in combination with scoring maintained an angulation significantly closer to the desired 90 degrees than cartilage scoring or cartilage suturing only(p<0.05). Histological analysis demonstrated a significant increase in cartilage hyperplasia by suturing alone, whereas the other techniques achieved only mild to moderate increases. We recommend cartilage scoring and suturing through skin incision on severe degrees of prominent ear, and cartilage needle scoring and buried suturing through slit incision on mile-to-moderate degrees of prominent ear.
Animals
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Cartilage
;
Ear*
;
Hyperplasia
;
Needles
;
Rabbits*
;
Skin
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Splints
;
Sutures
2.A case of baboon synrome due to mercury smoke of an amulet.
Jin Ho HONG ; Seung Hyun HONG ; Kee Chan MOON
Korean Journal of Dermatology 1993;31(4):607-611
Baboon syndrome is used to denote a systemic allergic contact dermititis with a characteristic color and distribution pattern. It is also referred to as mercury exanthem, because inhalation of mercury vapor usually causes the skiri lesion in a sensitized person. Diffuse pi,ikish erythema of the buttock, upper inner thigh, and axilla are characteristic features. We report a case of baboon syndrome developed after exposure to the smoke of a burning amulete a charm written on a piece of paper in a 12 year-old female. Mercury sensitivity was confirrned by a patch test. Atomic absorption by a spectrographic method and Scanning electron microscopy/energy dispersive for analysis X-ray detected mercury in the urine and the ed scraped pigments from the amulet, respectively.
Absorption
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Axilla
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Burns
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Buttocks
;
Child
;
Erythema
;
Exanthema
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Female
;
Humans
;
Inhalation
;
Papio*
;
Patch Tests
;
Smoke*
;
Thigh
3.Septoplasty through open rhinopasty.
Jin Soo KO ; Moo Hyun PAIK ; Seung Hong KIM
Journal of the Korean Society of Aesthetic Plastic Surgery 2000;6(1):36-43
No abstract available.
4.REPAIR OF NERVE DEFECTS WITH EXPANSION TECHNIQUE: HISTOMORPHOMETRIC STUDY ON NERVE REGENERATION.
Cheol Kyu KIM ; Seung Han KIM ; Seung Hong KIM ; Jin Soo KIM ; Mee Kyung KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1997;24(5):908-916
No abstract available.
Nerve Regeneration*
5.Five Cases of Agminated Lentigines.
Seung Hyun HONG ; Jin Ho HONG ; Hae Jun SONG ; Chil Hwan OH
Korean Journal of Dermatology 1995;33(5):983-987
Agminated lentigines may be defind as a circumscribed grouping of small pigmented macules arranged in a small or large group, often in a segmental pattern, each macule consisting of a lentiginous epidermal proliferation of melanocytes. We report five cases of agminated lentigines in otherwise healthy persons. Histologic exarnination of the pigmented lesion revealed findings consistent with lentigo simplex.
Humans
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Lentigo*
;
Melanocytes
6.The Effect of Tricyclic Antidepressant(Dothiepin) on Sleep in Depressed Patients: A Polysomnographic Study.
Seung Chul HONG ; Jin Hee HAN ; Sung Pil LEE ; Seung Kyu BANG
Journal of Korean Neuropsychiatric Association 1998;37(4):728-736
OBJECTIVE: This study was designed to investigate 1) sleep changes after antidepressant(dothiepin) treatment, and 2) sleep variables which seem to be associated with clinical response in the depressed patients. METHODS: The subjects consisted of 16 patients who fullfilled the criteria for major depression by the Diagnostic and Statistical Manual,(4th edition). Their sleep was recorded using polysomnography at the baseline and after one week and three weeks of dothiepin treatment. All subjects were further interviewed using Hamilton Rating Scale for Depression (HRSD) to rate the severity of their depression. High response to the drug was defined as a reduction of more than 50% of the HRSD score. Result : The results were as follows : 1) Depressed patients after dothiepin treatment showed more total sleep time(p=0.019), shorter sleep latency(p=0.05), less awake time(p=0.033), more sleep efficiency(p=0.018), more stage 2 sleep(p=0.002), less REM time(p=0.000), and longer REM sleep latency(p=0.004) than before treatment. 2) There were no differences in sleep variables between those who received 1 week and 3 weeks of dothiepin treatment except of th shortening of sleep latency after 3 weeks(p<0.05). 3) Depressive symptom scores on HRSD were reduced after 1 week and 3 weeks of dothiepin treatment as compared with the baseline. 4) High responers showed a tendency of increased wake time(p=0.054), while their stage 4 sleep decreased after 1 week of dothiepin treatment as compared with the low responders(p=0.0136). Conclusions : These results suggest that sleep of the depressed patients after dothiepin treatment tends to be nomalized and sleep chages seem to appear early in the treatment phase. In addition, clinical response might be associated with greater wake time at the baseline and lesser atage 4 sleep 1 week of dothiepin treatment.
Depression
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Dothiepin
;
Humans
;
Polysomnography
;
Sleep, REM
7.Intratendinous Tophaceous Gout Mimicking Cellulitis after Achilles Tendon Repair
Woo Jin SHIN ; Sung-Ha HONG ; Seung-Pyo SUH ; Seung Gi LEE
The Journal of the Korean Orthopaedic Association 2021;56(3):261-265
A diagnosis of gout is often straightforward because gout has well known clinical presentations, laboratory analyses, and radiologic features. On the other hand, gout can mimic other diseases by showing a range of atypical clinical manifestations. This paper reports a 35-year-old male with no prior history of gout who developed tophaceous gout at his previously repaired Achilles tendon 11 years after surgery. He was initially misdiagnosed with cellulitis because of his atypical clinical features. This case is presented with a review of the relevant literature.
8.A Case of Polygrandular Automune type II syndrome associated empty sella.
Jin Soo KIM ; Mi Duk LEE ; Hong Seung KIM ; Choon Hee CHUNG
Journal of Korean Society of Endocrinology 1998;13(2):295-300
The polyglandular autoimmune(PGA) syndrome designate as the dysfimction of endocrine and nonendocrine systems involving two or more organs on the basis of an autoimmune mechanism. There are 3 types of PGA syndrome and their etiology or pathogenesis is still not complete by understood. Type I PGA is present in the patients who have at least two of the triad of Addison's disease, hypopacathyroidism, and chronic mucocutaneous candidiasis. Type II PGA is present in the those who have Addisons disease with autoimmune thyroid disease and/or insulin dependent diabetes mellitus, but who do not have hypoparathyroidism or candidiasis. Type III PGA is present in the one who have autoimmune thyroid disease, without Addisons disease, but with another autoimmune disease report a case of autoimmune polyglandular syndrome type II in a seventy-three years old female patient who had primary adrenal insufficiency, primary hypothyroidism, and empty sella, pulmonary tuberculosis.
Addison Disease
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Autoimmune Diseases
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Candidiasis
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Candidiasis, Chronic Mucocutaneous
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Diabetes Mellitus
;
Female
;
Humans
;
Hypoparathyroidism
;
Hypothyroidism
;
Insulin
;
Polyendocrinopathies, Autoimmune
;
Thyroid Diseases
;
Tuberculosis, Pulmonary
9.Three Cases of Mobius Syndrome in a Family.
Hwan Mo JEONG ; Seung Hee HONG ; Dong Jin SHIN
Journal of the Korean Neurological Association 1996;14(4):1035-1041
Mobius syndrome is generally considered to be a static disorder of congenital origin, and is manifested as unilateral or bilateral facial weakness and lateral gaze limitation. In most instances the syndrome occurs sporadically, but rarely familial cases have been reported. We report a family of three members with Mobius syndrome; a 7-year-old girl, a 6-year-old boy, and their 29-year-old mother. Each patient revealed facial diplegia, and unilateral or bilateral lateral rectus palsy. Brain MRI scans showed normal and there were no definite brainstem dysfunctions on electrophysiologic studies.
Abducens Nerve Diseases
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Adult
;
Brain
;
Brain Stem
;
Child
;
Female
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Mobius Syndrome*
;
Mothers
10.Three Cases of Mobius Syndrome in a Family.
Hwan Mo JEONG ; Seung Hee HONG ; Dong Jin SHIN
Journal of the Korean Neurological Association 1996;14(4):1035-1041
Mobius syndrome is generally considered to be a static disorder of congenital origin, and is manifested as unilateral or bilateral facial weakness and lateral gaze limitation. In most instances the syndrome occurs sporadically, but rarely familial cases have been reported. We report a family of three members with Mobius syndrome; a 7-year-old girl, a 6-year-old boy, and their 29-year-old mother. Each patient revealed facial diplegia, and unilateral or bilateral lateral rectus palsy. Brain MRI scans showed normal and there were no definite brainstem dysfunctions on electrophysiologic studies.
Abducens Nerve Diseases
;
Adult
;
Brain
;
Brain Stem
;
Child
;
Female
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Mobius Syndrome*
;
Mothers