1.Adrenogenital Syndrome Combined with Congenital Hypothyroidism.
Jong Woon CHOI ; Woo Sik CHEONG ; In Kyu YI
Journal of the Korean Pediatric Society 1994;37(11):1607-1609
No abstract available.
Adrenogenital Syndrome*
;
Congenital Hypothyroidism*
2.Clinical Study of Mycoplasma Pneumoniae Infection in Children.
Jong Woon CHOI ; Hoan Jong LEE ; Byung Kiu PARK ; Hyung Ro MOON
Journal of the Korean Pediatric Society 1990;33(3):315-323
No abstract available.
Child*
;
Humans
;
Mycoplasma pneumoniae*
;
Mycoplasma*
;
Pneumonia, Mycoplasma*
3.Clinical Consideration of Coarctation of the Aorta.
Jong Woon CHOI ; Kyung Hee PARK ; Jung Yun CHOI ; Yong Soo YOON
Journal of the Korean Pediatric Society 1990;33(5):651-657
No abstract available.
Aortic Coarctation*
4.A Case of Systemic Fibromuscular Dysplasia with Renovascular Hypertension and Superior Mesenteric Arterial Aneurysm.
Jong Woon CHOI ; Sang Min YOON ; Young Chae JOO
Journal of the Korean Pediatric Society 1997;40(6):872-876
No abstract available.
Aneurysm*
;
Fibromuscular Dysplasia*
;
Hypertension, Renovascular*
5.Surface ECG Findings of the Patients with Left Isomerism.
Jae Kon KO ; Seong Ho KIM ; Jong Woon CHOI ; Dug Ha KIM ; Heung Jae LEE
Korean Circulation Journal 1991;21(6):1237-1241
Surface ECG findings in 29 patients with left isomerism were reviewed. Among the total 46 wave axis distributions, 25(54%) were abnormal axis, not originated from sinus node. Congenital atrioventricular block was found in 2 children. 6 patients showed the bradycardia and junctional escape rhythm intermittently or persistently. 4 of them, not related with heart surgery, were much older than 2 patients who showed these ECG findings after heart surgery. These ECG findings suggested the possibility of occurrence of sinus node or subsidiary pacemaker dysfunction in the patients with left isomerism, especially in the older patients. So we thought that electrophysiologic evaluation is necessary in some patients with left isomerism.
Atrioventricular Block
;
Axis, Cervical Vertebra
;
Bradycardia
;
Child
;
Electrocardiography*
;
Humans
;
Isomerism*
;
Sinoatrial Node
;
Thoracic Surgery
;
United Nations
6.Surface ultrastructure of Pygidiopsis summa (Digenea: Heterophyidae) adult flukes.
Jong Yil CHAI ; Woon Mok SOHN ; Sung Yil CHOI ; Soon Hyung LEE
The Korean Journal of Parasitology 2002;40(3):107-112
A scanning electron microscopic study was performed on the surface ultrastructure of Pygidiopsis summa (Digenea: Heterophyidae) adults. Metacercariae were collected from gills and muscles of mullets (Mugil cephalus) caught in a known endemic area, and adult flukes were harvested from dogs after 8 weeks of experimental infection. The worm was calabash form with its posterior part broader than the anterior part. Tegumental spines were densely distributed over the body surface, except on the suckers and genital apparatus, and around the excretory pore. Well differentiated spines were observed on the anterior half of the body, with 14-16 tips ventrally, and 19-20 tips dorsally. On the oral sucker, three pairs of type I sensory papillae (uni-ciliated knob-like swellings) and one pair of type II sensory papillae (aciliated round-swellings) were observed on the anterior and posterior parts of the lip, respectively. On the lip of the ventral sucker, one pair of type II sensory papillae was distributed only on its posterior part. Sperms were seen emerging from or entering into the genital apparatus. The results showed that the surface ultrastructure of P. summa was unique among the heterophyid trematodes, especially in digitation of tegumental spines and in distribution of sensory papillae on oral and ventral suckers.
Animals
;
Dogs
;
Heterophyidae/*ultrastructure
;
Microscopy, Electron, Scanning
7.Neuroblastoma : Computed Tomographic Finding.
Jae Woon KIM ; Jong Oh CHOI ; Jae Ho CHO ; Mi Soo HWANG ; Bok Hwan PARK
Yeungnam University Journal of Medicine 1996;13(1):134-140
Recently many studies have shown the usefulness of computed tomogram in diagnosing abdominal mass when clinical and conventional radiologic examinations fail to reveal the nature of abdominal mass or the cause of abdominal distension. To evaluate the usefulness of CT in diagnosing neuroblastoma, we retrospectively analyzed computed tomographic findings of 16 neuroblastoma patients, who pathologically proved in Yeungnam University Hospital from 1986 to 1995. The age range of the patients studied were from 8months to 18years. The most frequent sith of origin was adrenal gland and the next was retroperitioneum. The presenting symptoms were palpable mass, abdominal distension, and abdominal pain.- The viewpoints of this analysis were tumoral calcifications, midline cross, shape, margin, internal structure, contrast enhancement patterns, major vessel involvement, and lymph node involvement. ':haracteristic CT findings were 'as follows: Fine dense curvillinear calcification within the tumor(56%), midline cross(50%), lobulation(75%), well-circumscribed margin(56%), cystic degeneration(56%), heterogeneous contrast enhancement(690/o), encasement of major vessels such as aorta, IVC and celiac trunk(50%), and paraaortic lymphadenopathy(87%). We conclude that these CT findings were very common and could be helpful in diagnosting and differentiation neuroblastoma in infant and children.
Adrenal Glands
;
Aorta
;
Child
;
Diagnosis
;
Humans
;
Infant
;
Lymph Nodes
;
Neuroblastoma*
;
Retrospective Studies
8.A Case of Protein-losing Enteropathy in Congestive Heart Failure : Resolution with Prednisolone.
Journal of the Korean Pediatric Society 2001;44(5):587-591
Protein-losing enteropathy can result from primary or secondary intestinal lymphangiectasia. Sec ondary intestinal lymphangiectasia develops as a result of lymphatic obstruction or elevated lym phatic pressure. Cardiac lesions such as constrictive pericarditis, post-Fontan procedure state, and chronic congestive heart failure increase lymphatic pressure and may cause intestinal lymphan giectasia and protein-losing enteropathy. An 11-year-old girl who underwent corrective surgery for Tetralogy of Fallot at two years of age had been suffering from chronic congestive heart failure, taking digitalis and diuretics. She was afflicted with protein-losing enteropathy nine years after surgery. Diagnosis was made by means of radioisotope scan using technetium-99m-labeled albumin. Symptoms were not improved with diet therapy, so prednisolone was given orally and remission was achieved. Although relapses occurred four times, remission was achieved with pre dnisolone at each time. Thereafter the patient remained in remission state over one year after dis continuation of prednisolone.
Child
;
Diagnosis
;
Diet Therapy
;
Digitalis
;
Diuretics
;
Estrogens, Conjugated (USP)*
;
Female
;
Heart Failure*
;
Humans
;
Pericarditis, Constrictive
;
Prednisolone*
;
Protein-Losing Enteropathies*
;
Recurrence
;
Tetralogy of Fallot
9.Clinical Review of Recurrent Kawasaki Disease.
Jong Woon CHOI ; Soon Ki KIM ; Byong Kwan SON
Journal of the Korean Pediatric Society 1996;39(8):1139-1145
PURPOSE: The recurrence of Kawasaki disease has not been considered significant and has not been reported on literatures in Korea. Authors reviewed cases with recurrent Kawasaki disease to get informations about recurrent Kawasaki disease and to know whether there is any factor, if present, that can predict recurrence. METHODS: We reviewed and analyzed the hospital records of patients with recurrent Kawasaki disease who had been admitted to Inha University Hospital from January 1986 through December 1994. RESULTS: The total number of cases with Kawasaki disease was 266 during that period in Inha University Hospital. Seven patients were diagnosed as having recurrent Kawasaki disease, but four of them fulfilled five or more items of the diagnostic criteria for Kawasaki disease. So the proportion of recurrent cases was 1.5%(4/259)(or 2.7% (7/259) ?). Sex ratio was M:F=3:1. The ages at the first episodes of illness were from 7 months to 3 years 2 months (median=24 months), and those of the second episodes were from 11 months to 6 years 3 months (median=4 years 3 months). The intervals between two episodes were from 4 months to 4 years 2 months (median=1 year 9 months). No special aspect could be found in the clinical and laboratory findings of primary cases, compared with other cases with kawasaki disease. The clinical manifestations and courses of recurred cases were not significantly different from those of primary cases, except one recurred case who developed coronary aneurysm. CONCLUSIONS: The recurrence rate of Kawasaki disease seems to be higher than 1.5%(or 2.7%) at least. The risk factors for recurrence could not be found, and there was no specific aspect in the clinical manifestations and courses of recurrent Kawasaki disease.
Coronary Aneurysm
;
Hospital Records
;
Humans
;
Korea
;
Mucocutaneous Lymph Node Syndrome*
;
Recurrence
;
Risk Factors
;
Sex Ratio
10.Two Cases of Ureterocele.
Jong Han CHOI ; In Ho SONG ; Woon Hyung LEE
Korean Journal of Urology 1971;12(1):113-116
No abstract available.
Ureterocele*