1.Diabetes mellitus as a predictor for late recovery of vestibular neuritis
Kang Min Park ; BongSoo Park ; Kyong Jin Shin ; Sam Yeol Ha ; JinSe Park ; Sung Eun Kim
Neurology Asia 2014;19(4):393-397
The time course of recovery in vestibular neuritis varies between individuals. The aim of this study was
to identify the predictors for the early or late recovery of vestibular neuritis. The inclusion criteria were
patients 1) who had an acute onset of vertigo lasting at least 24 hours, 2) with a horizontal-torsional
unidirectional spontaneous nystagmus, and 3) with a canal paresis of 20% or more on the bithermal
caloric tests. The primary endpoint for this study was an early or late recovery of vestibular neuritis as
a dependent variable. A functional level scale was used to define the late recovery (5 or more points) at
seven days after the symptom onset. The secondary endpoint was the duration of hospitalization. One
hundred twenty eight patients met the inclusion criteria for this study, and among them, 71 patients
had an early recovery. Multiple logistic regression analysis showed that diabetes mellitus was the only
independent significant variable for the prediction of a late recovery of vestibular neuritis. In addition,
the diabetes mellitus was a predicting variable for long duration of hospitalization. Diabetes mellitus
was a predictor for a late recovery of vestibular neuritis.
2.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
3.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*
4.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.
5.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
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
8.Cytologic Findings of Parathyroid Carcinoma: Report of Two Cases.
Yun Hee JIN ; Yong Wook PARK ; Mi Sheon JIN ; Seung Sam PAIK ; Se Jin JANG ; Moon Hyang PARK
Korean Journal of Cytopathology 2003;14(1):1-6
Parathyroid carcinoma is a rare disorder accounting for 0.5% to 5% of parathyroid neoplasia. Diagnosis of parathyroid carcinoma in fine needle aspiration cytology(FNAC) is difficult because all characteristic features of parathyroid carcinoma can be recognized in parathyroid adenoma or hyperplasia. Cellular atypism cannot be used for the diagnostic criteria of parathyroid carcinoma as malignancies of most other organs. We experienced two cases of cytologic features of parathyroid carcinoma confirmed by histologic examination. The majority of tumor cells formed large cohesive clusters, although individual tumor cells were also present. The tumor cells displayed rather pleomorphic round to oval nuclei, occasional prominent nucleoli, and distinct cytoplasmic margin. Occasionally karyolysis, anuclear cells, and nonepithelial cell clusters were noted. The histologic findings showed a partially lobulated architecture, with admixture of sheets of chief cells, oxyphil cells, and occasional water clear cells. The tumor infiltrated into the thyroid parenchyme and perithyroidal soft tissue. The electron microscopic study of case 1 disclosed typical findings of parathyroid neoplasm; clusters of secretory chief cells with centrally located round to ovoid nuclei, moderately clumped heterochromatins and one or two nucleoli. The tumor cells showed conspicous interdigitation of contiguous cell membrane and intercellular microvilli.
Biopsy, Fine-Needle
;
Cell Membrane
;
Cytoplasm
;
Diagnosis
;
Heterochromatin
;
Hyperplasia
;
Microscopy, Electron
;
Microvilli
;
Oxyphil Cells
;
Parathyroid Neoplasms*
;
Thyroid Gland
;
Water
9.Effect of Partial Glossectomy on Speech of Down Syndrome Children.
Yong Sam PARK ; Won Yong YANG ; Jin Young KIM ; Su Jung KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 2001;28(3):289-294
The anatomy of oral cavity in Down syndrome is characterized by hypotonic macroglossia, small oral cavity, and narrow palate with high-arch shape. Because of such characteristics, patients show difficulty in articulation, resonance and phonation. They also suffer from respiratory difficulty due to narrow upper respiratory tract which is exaggerated by hypertrophied tonsil and adenoid. So far we operated on 100 children with Down syndrome for partial glossectomy in average volume of 4.6 cc. We analyzed the results by means of questionnaires and speech test with multi-speech model 3700 program before and after the operation. After partial glossectomy, we observed that they could close their lips comfortably, and it can mitigate the stigma of Down syndrome. We could also observe the improvement in voice quality, pitch, resonance and articulation. Through paired t-test using SAS, we analyzed value of F1, F2-F1, and changes of fundamental frequency(Fo). After partial glossectomy, anteriorly positioned tongue of Down patients became significantly smaller in size and be located posteriorly.
Adenoids
;
Child*
;
Down Syndrome*
;
Glossectomy*
;
Humans
;
Lip
;
Macroglossia
;
Mouth
;
Palate
;
Palatine Tonsil
;
Phonation
;
Surveys and Questionnaires
;
Respiratory System
;
Tongue
;
Voice Quality
10.Clinical Approach of Ultrasonography in the Diagnosis of Intussusception in Infant and Children.
Hee Tang LIM ; Jin Kil PARK ; Hong Ju CHOI ; Jae Sam KIM ; Hyo Kyung SHIN ; Chul Hoi GU
Journal of the Korean Pediatric Society 1994;37(5):649-654
Thirty consecutive patient seen in a pediatric out patient and emergency department, in whom the diagnosis of intussusception was considered, had an ultrasound examination of the abdomen before the barium enema. The peak age was 5~12 month (range 4~34 month). Intussusception was detected by ultrasonography in all 25 cases proved by barium enema (sensitivity 100%). Normal findings on ultrasonography correlated with a negative barium enema results in 5 of 5 cases (negative predictive value=100%). No intussusception was missed by ultrasonography. To determine which patient would most benefit from ultrasonography, we divided patients into either a high risk group (100% intussusception) or a low risk group (37.5% intussusception) on the basis of clinical symptoms. We conclude that ultrasonography can be used as a rapid sensitive screening procedure in the diagnosis or exclusion of childhood intussusception. Probability of surgical reduction was associated with size of of total thickness and external rim thickness.
Abdomen
;
Barium
;
Child*
;
Diagnosis*
;
Emergency Service, Hospital
;
Enema
;
Humans
;
Infant*
;
Intussusception*
;
Mass Screening
;
Ultrasonography*