2.A study on the quantitative evaluation of hoarseness using sonograph.
Young Sam YOO ; Kwang Hyun KIM ; Jin Young KIM
Korean Journal of Otolaryngology - Head and Neck Surgery 1991;34(1):148-158
No abstract available.
Evaluation Studies as Topic*
;
Hoarseness*
3.Effect of SOD Pretreatment on Ultrastructural Changes in Rectus Femoris Muscle of Rats After Irradiation.
Doo Jin PAIK ; Kyu Hee HAN ; Ho Sam CHUNG
Korean Journal of Anatomy 1998;31(4):513-524
Irradiation which acts directly and produces the reactive oxygen radicals by ionizing water molecules, causes significant morbidity and mortality. The muscle is damaged by direct action, oxygen radicals and the alterations of microcirculation and metabolism after irradiation. The changes of SOD immunoreactivities in muscles of the rats after irradiation were observed. The ultrastructural changes of the irradiated muscles with the pretreatment of SOD (superoxide dismutase) or without were also investigated. A total of 60 healthy Sprague-Dawley male rats weighing from 200g to 250g were used as experimental animals. Under urethane (1.15g/kg. IP.2 times) anesthesia,30 Gy irradiation to lower extremities by PICKER-C9 Cobalt-60 teletherapy unit was done. 15,000 unit/kg of SOD was administered intraperitoneally 1 hour before irradiation. The experimental animals were sacrificed 1 day, 3 days, 7 days, 2 weeks and 4 weeks after irradiation. The superficial portions of the mid-belly of the rectus femoris muscles were obtained and sliced into portions, 2 mm in length, 1 mm in width and in thickness. The specimens were prepared by routine methods for the electron microscopic observation. All preparations were stained with uranyl acetate and lead citrate and observed with a Hitachi-600 electron microscope. The other parts of mid-belly of the rictus femoris muscles were sectioned in 14 micrometer thickness with cryostat at -20 degrees C. The immunoreactivities of SOD by use of antihuman Cu, Zn-and Mn-SOD antibodies were observed. The results were obtained as follows . 1. After irradiation, the immunoreactivities of SOD in the rictus femoris muscle were decreased. 2 weeks after irradiation, the immunoreactivities of Cu, Zn-SOD were trace, which was lowest.4 weeks after irradiation, the immunoreactivities were trace or weak. 1 day after irradiation, the immunoreactivities of Mn-SOD were trace, which was lowest. The immunoreactivities of Mn-SOD were increased gradually 4 weeks after irradiation, the immunoreactivities of Mn- SOD were moderate or weak. 2. The ultrastructural changes in the rectus femoris muscles of the rats were getting severer and severer after irradiation. 2 weeks after irradiation, unclear A band and I band, myofibrillolysis, increased and dilated cistemae of sarcoplasmic reticulum and mitochondria with dilated cristae and electron lucent matrix were seen. 4 weeks after irradiation, lysis of sarcomere and increased cisternae of sarcoplasmic reticulum were seen. 3. The ultrastructural changes in the rectus femoris muscles of the rats were getting worse and worse after 3 days of irradiation with the pretreatment of SOD. 2 weeks after irradiation with the pretreatment of SOD, myofibrillolysis, increased and dilated cisternae of sarcoplasmic reticulum and damaged mitochondria were seen. 4 weeks after irradiation with the pretreatment of SOD, the ultrastructures of rectus femoris muscles were recovered to normal. Consequently, after irradiation of 30 Gy, the immunoreactivities of SOD are decreased and SOD attenuates the reversible changes of ultrastructures in muscles.
Animals
;
Antibodies
;
Citric Acid
;
Humans
;
Lower Extremity
;
Male
;
Metabolism
;
Microcirculation
;
Mitochondria
;
Mortality
;
Muscles
;
Quadriceps Muscle*
;
Rats*
;
Rats, Sprague-Dawley
;
Reactive Oxygen Species
;
Sarcomeres
;
Sarcoplasmic Reticulum
;
Superoxide Dismutase
;
Urethane
4.A Case of Hereditary Anhidrotic Ectodermal Dysplasia.
Jong Won LEE ; Jin Kyung JUNG ; Jin Gun BANG ; Jin Sam RHO ; Jung Hee PARK
Journal of the Korean Pediatric Society 1994;37(10):1453-1456
Hereditary anhidrotic ectodermal dysplasia is a rare condition characterized by underdeveloped ectodermal structure including the skin, teeth or skin appendages. The patient has characteristic feature of anhidrosis, hypotrichosis and defective dentition. We experienced a case of hereditary anhidrotic ectodermal dysplasia in a l-month-old male infant who had unexplained recurring fever, anhidrosis and characteristic facial feature, so we established the diagnosis with clinical feature and skin biopsy.
Biopsy
;
Dentition
;
Diagnosis
;
Ectoderm
;
Ectodermal Dysplasia*
;
Fever
;
Humans
;
Hypohidrosis
;
Hypotrichosis
;
Infant
;
Male
;
Skin
;
Tooth
5.A Case of palisaded, Encapsulated Neuroma.
Seok Jin HONG ; Sam Hyeong KIM ; Hoon KANG ; Sook Ja SON ; Hee Jin JANG
Korean Journal of Dermatology 1998;36(1):173-176
Palisaded, encapsulated neuroma is characterized clinically by a solitary, slowly-growing and dome-shaped papule or nodule, usually accompanied by telangiectasia on the surface, and histopathologically by an encapsulated nodule in the dermis and the palisading arrangement of nuclei. A 57-year-old female patient presented with a 1cm-sized, solitary nodule on the right ala nasi which had been present for about 5 years. The nodule had a tendency to slow growth and it became a polypoid nodule. Telangiectasia was shown on the surface of the lesion. Histopathlogical findings showed a well-defined and encapsulated nodule in the dermis, composed of spindle cells with basophilic and plump nuclei in a palisading fashion. On immunohistochemical staining, the tumor cells of the nodule were positive for S-100 protein, while the capsule of the nodule was negative for S-100 protein. Epithelial membrane antigens were focally positive only on the capsule of the nodule. We report herein a case of palisaded, encapsulated neuroma, one case of which has been reported in Korea.
Basophils
;
Dermis
;
Female
;
Humans
;
Korea
;
Middle Aged
;
Mucin-1
;
Neuroma*
;
S100 Proteins
;
Telangiectasis
6.A case of incontinentia pigmenti.
Soo Am CHUNG ; Won Rae KIM ; Hyung Kun NAM ; Jin Sam NO ; Jung Hee PARK
Journal of the Korean Pediatric Society 1993;36(3):428-433
Down syndrome is the most common autosomal chromosomal abnormality characterized by mental and growth retardation, and by various typical features including prominent epicanthal fold, oblique palpebral fissure, flat nasal bridge, short and broad hand, wide toe interspace, etc. The overall incidence has been shown to be 1:800 deliveries, increasing with advancing maternal age. However, twin cases are extremely rare, and thus far only 500 cases were reported worldwide. We have recently observed 10-day-old male monozygotic twins with Down syndrome, born to a mother of 30 years of age with one normal child. Both have VSD confirmed by 2D-echocardiography, in addition to various typical features. Cytogenetic examination revealed that both have karyotypes of 47, XY, +21. This is the first report in Korea as the authors are aware of.
Child
;
Chromosome Aberrations
;
Cytogenetics
;
Down Syndrome
;
Hand
;
Humans
;
Incidence
;
Incontinentia Pigmenti*
;
Karyotype
;
Korea
;
Male
;
Maternal Age
;
Mothers
;
Toes
;
Twins, Monozygotic
7.Inflammatory Myofibroblastic Tumor in Posterior Mediastinum.
Seung Sam PAIK ; Seok Hoon JEON ; Se Jin JANG ; Moon Hyang PARK ; Jung Dal LEE
Korean Journal of Pathology 1997;31(1):63-67
Inflammatory myofibroblastic tumor(IMT) or inflammatory pseudotumor is a rare, solid tumor that most often affects children. This tumor is characterized by a spindle cell proliferation admixed with a variety of inflammatory cells. Although it has disputed nosology, a distinctive fibroinflammatory and even pseudosarcomatous appearance have been well appreciated. Herein, we report a case of IMT in the posterior mediastinum in a 19-year-old girl with clinical findings. The immunohistochemical and ultrastructural studies on the tumor cells are reported, and their distinctive characteristics are discussed in details.
Cell Proliferation
;
Child
;
Female
;
Granuloma, Plasma Cell
;
Humans
;
Mediastinum*
;
Myofibroblasts*
;
Young Adult
8.A Case of Pseudallescheria boydii Mycetoma.
Sam Hyeong KIM ; Seok Jin HONG ; Hoon KANG ; Sook Ja SON ; Kyae Yong SONG
Korean Journal of Dermatology 1998;36(2):341-345
Pseudallescheria (P.) boydii is a true fungus that is ubiquitous in nature, and has a world-wide distribution. It has been isolated from soil, plant debris, polluted water and sewage. Infection may occur via direct inoculation or inhalation, and usually affects the extremities. It is a common cause of mycetoma characterized by tumefaction, draining sinuses and grains. It has polymorphism due to a complicated life cycle which undergoes teleomorph as well as anamorph stages. Cleistothecia, ascocarp and ascospore may be seen during the teleomorph stages, whereas scedosporium and graphium type may be seen during the anamorph stages. We report a case of P. boydii mycetoma occurring in a 69-year old male. He had multiple nodules with a discharging fistula on a dark red plaque at the dorsum of the right forearm. Cultural isolation for definitive diagnosis showed typical P. boydii. The lesion responded well to daily itraconazole.
Aged
;
Edible Grain
;
Diagnosis
;
Extremities
;
Fistula
;
Forearm
;
Fungi
;
Humans
;
Inhalation
;
Itraconazole
;
Life Cycle Stages
;
Male
;
Mycetoma*
;
Plants
;
Pseudallescheria*
;
Scedosporium
;
Sewage
;
Soil
9.A case of asphyxisting thoracic dystrophy.
Chang Hee BAE ; Jong Min LEE ; In Hee PARK ; Chin Sam RO ; Hyo Jin LEE
Journal of the Korean Pediatric Society 1991;34(6):832-836
No abstract available.
10.Effective Inhibition of Glomerulosclerosis by Adenoviral Vector Expressing Human IL-10.
Young Kook CHOI ; Yong Jin KIM ; Yong Hoon PARK ; Kyu Sam CHOI ; Jong Gu PARK
Korean Journal of Immunology 2000;22(3):187-195
No abstract available.
Humans*
;
Interleukin-10*