1.Comparison and correlation of carcinoembryonic antigen levels betwwen peripheral blood and inferior mesenteric vein blood, and gallbladder bile, and rectal secretion.
Byung Soo DO ; Yon Woong CHUNG ; Sang Woon KIM ; Jae Hwang KIM ; Min Chul SHIM ; Koing Bo KWUN
Journal of the Korean Society of Coloproctology 1991;7(2):105-111
No abstract available.
Bile*
;
Carcinoembryonic Antigen*
;
Gallbladder*
;
Mesenteric Veins*
2.A Case of Ureteritis Cystica.
Chan Euy CHUNG ; Do Gyun YANG ; Se Woong KIM ; Dong Hwan LEE ; Young Jai LEE
Korean Journal of Urology 1990;31(5):777-780
Ureteritis cystica is one of the cystic diseases formed in the mucosa or submucosa of the renal pelvic, ureter and bladder by chronic inflammation or irritation. A rare case of ureteritis cystica confirmed by ureteroscopy is presented with review of the literatures.
Inflammation
;
Mucous Membrane
;
Ureter*
;
Ureteroscopy
;
Urinary Bladder
3.The Relation between Idiopathic Macular Hole and Perifoveal Vitreous Detachment.
Do Hyun CHUNG ; Don Il HAM ; Se Woong KANG
Journal of the Korean Ophthalmological Society 2002;43(12):2430-2438
PURPOSE: To determine the relation between the pathogenesis of idiopathic macular hole and perifoveal vitreous detachment using OCT scan. METHODS: On 28 eyes with idiopathic macular hole stage 1,2,3 which was graded according to using the classification described by Gass and on 123 eyes from the normal contrast group, OCT scan were performed to obtain axial views of the vitreoretinal interface in the posterior pole. The incidence of perifoveal vitreous detachment was assessed. RESULTS: 18 of the 28 eyes (64.2%) from the macular hole group and 15 of the 123 eyes (12.1%) from the normal contrast group had perifoveal vitreous detachment on OCT scan. The difference was statistically significant (p<0.05).There was no statistically significant difference on the incidence of perifoveal vitreous detachment according to stage of macular hole. CONCLUSIONS: These results led to the conclusion that there is a significant relation between the pathogenesis of macular hole and the papillofoveal traction.
Classification
;
Incidence
;
Retinal Perforations*
;
Tomography, Optical Coherence
;
Traction
;
Vitreous Detachment*
4.Immunohistochemical Localization of Phospholipase D1 in Developing Rat Forebrain.
Jeong Sun CHOI ; Do Sik MIN ; Jin Woong CHUNG ; Myung Hoon CHUN ; Mun Yong LEE
Korean Journal of Anatomy 2001;34(4):427-434
Phospholipase D (PLD), one of the intracellular signal transduction enzymes, may play an important role in developing brain. However, the developmental regulation of PLD protein has not been determined. In the present study, we investigated the temporal and spatial expression of PLD isozyme, PLD1 in the developing rat forebrain using an affinity-purified peptide antibody against PLD1. Our data showed that immunoreactivity for PLD1 was first seen in the germinal zone of the lateral ventricle, differentiating neurons and their processes at embryonic day 18 (E18). At E20, clusters of immunoreactive cells were observed in the medial germinal zone of the lateral ventricle, restricted zones of the frontal and parietal cortex, the nuclei of the medial septum and the diagonal band. During the first postnatal week, there was an increase in the number and staining intensity of the immunoreactive neurons in the cerebral cortex, which peaked at postnatal day 7 (P7). During the second postnatal week, there was an abrupt decrease in the number of immunoreactive cortical pyramidal neurons. By P14, only a few of the pyramidal neurons in cerebral cortex layer V were immunoreactive. These results revealed that expression of PLD1 protein at various stages of development of the septum and cerebral cortex is differentially regulated. This suggests that PLD1 may regulate the developmental processes of some neuronal populations.
Animals
;
Brain
;
Cerebral Cortex
;
Immunohistochemistry
;
Lateral Ventricles
;
Neurons
;
Phospholipase D
;
Phospholipases*
;
Prosencephalon*
;
Rabeprazole
;
Rats*
;
Signal Transduction
5.A case of nephrogenic diabetes insipidus caused by obstructive uropathy due to prostate cancer.
Eun Gyoung HONG ; YuJin SUH ; Yoon Sok CHUNG ; Hyeon Man KIM ; Gyu Tae SHIN ; Do Young CHUNG ; Rae Woong PARK
Yonsei Medical Journal 2000;41(1):150-154
Nephrogenic diabetes insipidus (DI) secondary to chronic urinary tract obstruction is a rare disease. The exact cause is unknown but it is likely that increased collecting duct pressures cause damage to the tubular epithelium, resulting in insensitivity to the action of arginine-vasopressin (AVP). A 77-year-old man complaining of polyuria and polydipsia was treated with alpha glucosidase inhibitor under the impression of polyuria due to diabetes mellitus. But his symptoms did not improve. Water deprivation and AVP administration study revealed that the patient had nephrogenic DI. Urinary tract obstruction due to an enlarged prostate was suggested as a principal cause of nephrogenic DI. The patient underwent transurethral resection of the prostate and bilateral subcapsular orchiectomy. After surgery, the urine osmolarity was normalized and the patient became symptom-free. We report a case of nephrogenic DI due to obstructive uropathy which was cured by surgery eliminating obstruction.
Adenocarcinoma/ultrasonography
;
Adenocarcinoma/radionuclide imaging
;
Adenocarcinoma/pathology
;
Adenocarcinoma/complications*
;
Aged
;
Case Report
;
Constriction, Pathologic/etiology
;
Diabetes Insipidus, Nephrogenic/etiology*
;
Human
;
Male
;
Prostatic Neoplasms/ultrasonography
;
Prostatic Neoplasms/radionuclide imaging
;
Prostatic Neoplasms/pathology
;
Prostatic Neoplasms/complications*
;
Urologic Diseases/etiology*
6.Langerhans Cell Sarcoma in Two Young Children: Imaging Findings on Initial Presentation and Recurrence.
Woong Do CHUNG ; Soo Ah IM ; Nak Gyun CHUNG ; Gyeong Sin PARK
Korean Journal of Radiology 2013;14(3):520-524
Langerhans cell sarcoma (LCS) is a neoplastic proliferation of Langerhans cells with malignant cytological features and multi-organ involvement that typically has a poor prognosis. We experienced 2 cases of LCS in children less than 2 years of age and report them based primarily on CT and MR findings. Both children had findings of hepatosplenomegaly with low-attenuation nodular lesions, had multiple lymphadenopathy, and had shown recurrent lesions invading the skull during follow-up after chemotherapy.
Female
;
Hepatomegaly/diagnosis
;
Humans
;
Infant
;
Langerhans Cell Sarcoma/*diagnosis
;
Magnetic Resonance Imaging
;
Mediastinal Neoplasms/*diagnosis
;
Neoplasm Recurrence, Local
;
Skull Neoplasms/*diagnosis
;
Splenomegaly/diagnosis
;
Tomography, X-Ray Computed
7.Midline One-Stage Complete Unifocalization and Repair for Pulmonary Atresia, Ventricular Septal Defect associated with Major Aortopulmonary Collaterals: 1 case report.
Woong Han KIM ; Young Tak LEE ; Sub LEE ; Jung Hyeun BANG ; Wook Sung KIM ; Cheol Hyun CHUNG ; Chan Young NA ; Yoon Seop JEONG ; Jae Jin HAN ; Do Hyun CHUNG ; Ill Sang CHUNG ; Jung Won PARK ; Young Kwan PARK ; Sung Nok HONG
The Korean Journal of Thoracic and Cardiovascular Surgery 1997;30(5):524-527
Pulmonary atresia with ventricular septal defect and major aortopulmonary collaterals is a rare and complex lesion in which great morphologic variability exists regarding the sources of pulmonary blood flow. We report a case of this disease with no true central pulmonary arteries in a 9-month-old-boy successfully treated by one-stage complete unifocalization and repair from a midline sternotomy approach.
Heart Septal Defects, Ventricular*
;
Pulmonary Artery
;
Pulmonary Atresia*
;
Sternotomy
8.Bivenrticular Repair of Double Outlet Right Ventricle with Remote Ventricular Septal Defect.
Jung Hyeon BANG ; Young Tak LEE ; Jae Jin HAN ; Cheol Hyun CHUNG ; Woong Han KIM ; Chan Young NA ; Yoon Seop JEONG ; Wook Sung KIM ; Sub LEE ; Sang Ik KIM ; Il Sang CHUNG ; Jung Won PARK ; Do Hyun CHUNG ; Yung Kwan PARK ; Chong Wan KIM ; Sung Nok HONG
The Korean Journal of Thoracic and Cardiovascular Surgery 1997;30(7):641-646
Understanding of the surgical anatomy of patients with double outlet right ventricle (DORV) is important in the planning of biventricular repair. From May 1995 to September 1996, 7 patients underwent biventricular repair for DORV with remote ventricular septal defect. There were 5 males and 2 females. Age at operation varied from 2 to 9 years(mean 3.4+/-2.7years). Preoperative diagnostic assessment was made by two-dimensional echocardiography and cardiac catheterization. Ventricular septal defect was perimembranous inlet type in all patients. Associated cardiac anomalies were pulmonary atresia in two, pulmonary stenosis in five and tricuspid chordae attachment to conal septum in five. The operations were performed intraventricular repair and pulmonary enlargement in two, REV operation in two, and Rastelli operation in three. There was no early postoperative deaths and complications. The follow-up period was from 1 month to 18months, averaging 10+/-6.1 months. In the past,we considered the Fontan operation indicative as primary choice when DORV was associated with abnormal tricuspid chordal attachment to the conal septum,but now we believe that biventricular repair is feasible for those cases by making conal flap or reattachment method. Biventricular repair has theoretic advantages because it estabilishes normal anatomy and physiology,and it was concluded that the precise preoperative evaluation using both echocardiography and cardiac catheterization was essential to the successful surgery.
Bays
;
Cardiac Catheterization
;
Cardiac Catheters
;
Double Outlet Right Ventricle*
;
Echocardiography
;
Female
;
Follow-Up Studies
;
Fontan Procedure
;
Heart Septal Defects, Ventricular*
;
Humans
;
Male
;
Pulmonary Atresia
;
Pulmonary Valve Stenosis
9.The etiology of acute viral hepatitis for the last 3 years at a single institution in Seoul.
Jang Sik MUN ; Hyung Joon KIM ; Hue CHAE ; Sang Joong KIM ; Hong Ju MOON ; Hyun Woong LEE ; Chang Hwan CHOI ; Jae Hyuk DO ; Sae Kyung CHANG
Korean Journal of Medicine 2008;74(6):624-631
BACKGROUND/AIMS: Hepatitis A is increasing during the recent years in Korea, and sporadic cases of hepatitis E are not rare. We investigated the etiology of acute viral hepatitis, including 27 cases of coinfection with hepatitis A and E, during the last 3 years. METHODS: Retrospective analysis of one hundred eleven patients with acute viral hepatitis at Chung-Ang University Hospital was done from January 2005 to July 2007. The patients were positive for any one of the following tests: IgM anti-HAV, IgM anti-HBc, HCV RNA and IgM anti-HEV. RESULTS: The proportions of acute viral hepatitis A, B and C were 94.6% (105/111), 4.5% (5/111) and 0.9% (1/111), respectively. Among the patients with hepatitis A, 27 patients (24.3%) were positive for IgM anti-HEV. We analyzed 105 patients with either hepatitis A only or they had coinfection of hepatitis A and E. The mean age, the duration of the hospital stay, the mean levels of serum transaminase, bilirubin and albumin and the protrombin time were similar between the patients with hepatitis A only and those with coinfection of hepatitis A and E. All the patients were discharged without serious complication such as fulminant hepatic failure. The biochemical liver function tests were normalized in all patients within 8 weeks. CONCLUSIONS: The most common etiology of acute viral hepatitis in Koreans was the hepatitis A virus. Patients coinfected with hepatitis A and E were observed. The patients with coinfection of hepatitis A and E showed no significant difference in their clinical features and laboratory parameters, as compared to the patients with hepatitis A only.
Bilirubin
;
Coinfection
;
Hepatitis
;
Hepatitis A
;
Hepatitis A Antibodies
;
Hepatitis A virus
;
Hepatitis E
;
Humans
;
Immunoglobulin M
;
Korea
;
Length of Stay
;
Liver Failure, Acute
;
Liver Function Tests
;
Retrospective Studies
;
RNA
10.A Case of Undifferentiated Carcinoma with Osteoclast-Like Giant Cells in the Pancreas.
Suh Yoon YANG ; Jae Hyuk DO ; In Soo OH ; Hyun Woong LEE ; Chang Hwan CHOI ; Sae Kyung CHANG ; Eon Sub PARK
Korean Journal of Medicine 2011;80(1):82-86
Undifferentiated carcinomas with osteoclast-like giant cells are rare pancreatic and periampullary neoplasms that mimic giant cell tumors of bone morphologically. Recently, we experienced an osteoclast-like giant cell tumor arising in the tail of the pancreas. A 76-year-old male was admitted with epigastric discomfort and indigestion. Abdominal computed tomography (CT) and abdominal magnetic resonance imaging (MRI) showed a 3x3-cm mass containing necrotic and hemorrhagic areas in the tail of the pancreas. A distal pancreatectomy and splenectomy were performed. Histological examination showed tumor cell components consisting of mononuclear pleomorphic cells admixed with osteoclastic giant cells. The final diagnosis was undifferentiated carcinoma with osteoclast-like giant cells with ductal adenocarcinoma in the pancreas.
Adenocarcinoma
;
Aged
;
Carcinoma
;
Cellular Structures
;
Dyspepsia
;
Giant Cell Tumors
;
Giant Cells
;
Humans
;
Hydrazines
;
Magnetic Resonance Imaging
;
Male
;
Osteoclasts
;
Pancreas
;
Pancreatectomy
;
Splenectomy