1.A Case of Morgagni Hernia Confirmed by Diagnostic Pneumoperitoneum.
Young Mi HONG ; Hae Seung KIM ; Joong Gon KIM ; Keun LEE ; Seung Yeul YOO
Journal of the Korean Pediatric Society 1982;25(12):1266-1269
No abstract available.
Hernia*
;
Pneumoperitoneum*
2.Transcatheter Closure of Patent Foramen Ovale in a Stroke Patient under the Guidance of Transesophageal Echocardiography.
Sang Sig CHEONG ; Sang Gon LEE ; Myeong Ki HONG ; Seong Wook PARK ; Seung Jung PARK
Korean Circulation Journal 1996;26(3):731-733
Interest in the prevalence of patent foramen ovale(PFO) and its relation to embolic stroke has increased with the sophistication of methods for noninvasive cardiac assessment. The effect of foramen ovale closure on the risk for subsequent strokes is promised. A 22-year old woman was presented with sudden onset of cerebral infarct. She had a patent formen ovale, and right to left shunt during the Valsalva maneuver, which was diagnosed by transesophageal contrast echocardiography. Transcatheter closure of PFO was performed with Rashkind PDA umbrella under the guidance of transesophageal echocardiography. Transcatheter closure of PFO can be accomplised with little morbidity and may reduce the risk of embolic episode.
Echocardiography
;
Echocardiography, Transesophageal*
;
Female
;
Foramen Ovale
;
Foramen Ovale, Patent*
;
Humans
;
Prevalence
;
Stroke*
;
Valsalva Maneuver
;
Young Adult
3.A Case of Adrenal Cavernous Hemangioma.
Jeong Oh LEE ; Seung Hun JEON ; Yang Hoo KIM ; In Gon KIM ; In Gi SEONG ; Bo Hyun HAN
Korean Journal of Urology 2000;41(6):803-806
No abstract available.
Hemangioma, Cavernous*
4.Radiologic findings of osteochondritis dissecans.
Jae seung KIM ; Choong Gon CHOI ; Heung Sik KANG ; Seon Kyu LEE ; Chu Wan KIM
Journal of the Korean Radiological Society 1993;29(3):528-534
To evaluate the radiographic characteristics of osteochondritis dissecans (OCD) and useful parameter for predicting mechanical stability, we retrospectively analysed 26 plain radiographic examinations and seven MR imagings in 28 cases of OCD in 24 patients. Typical radiologic findings were osteochondral defect with sclerotic rim of variable thickeness and osteochondral fragment. Sites of osteochondral defect were medial (35.9%) or lateral (32%) femoral chondyle and medial (7.1%) or lateral (25%) side of talar dome. Sclerotic rim was seen in 24 cases (85%) and osteochondral fragments including nine loose bodies were seen in 21 cases (75%). The size of osteochondral defect with unstable fragment (average 2.05cm) and loose body (2.04cm) in the knee joint were similar to, but statistically larger than that with stable fragment (1.35cm). All osteochondral defects were well visualized on MR images. Abnormalities of articular cartilage and effusion in the interface between the parent bone and fragment were seem in five cases of which there were confirmed three unstable cases arthroscopically. We conclude that size of defect may be a good parameter for predicting mechanical stability and MRI may be useful in the diagnosis of OCD and determining the methods of treatment.
Cartilage, Articular
;
Diagnosis
;
Humans
;
Knee Joint
;
Magnetic Resonance Imaging
;
Osteochondritis Dissecans*
;
Osteochondritis*
;
Parents
;
Retrospective Studies
5.A Case of Potter Syndrome.
Young Mi HONG ; Hae Seung KIM ; Jung Gon KIM ; Keun LEE
Journal of the Korean Pediatric Society 1982;25(11):1181-1184
No abstract available.
6.A Case of Carcinosarcoma of Ovary.
Hyun Jin PARK ; Seung Pil LEE ; Jae Pyang SIM ; Heung Gon KIM ; Kie Jung YUN
Korean Journal of Obstetrics and Gynecology 2000;43(9):1670-1673
No abstract available.
Carcinosarcoma*
;
Female
;
Ovary*
7.A Case of Impetigo Herpetiformis during Pregnancy.
Seong Pil LEE ; Seong Jin HONG ; Su Mi OH ; Heung Gon KIM ; Seung Hun CHA
Korean Journal of Obstetrics and Gynecology 1999;42(8):1864-1868
Impetigo herpetiformis is a rare pustular eruption that may be seen in late pregnancy. It is associated with severe maternal and fetal complications in case of misdiagnosis and delayed treatment. The patient was a 25-years-old multigravida with psoriasis in her past history. At 20weeks gestation, she had been developed erythematous scaly annular patchs with papules and pustules on inner thigh. At 37weeks' gestation, the patient was suffered from a severely pruritic pustular rash with fever and leukocytosis. The skin of the affected areas was biopsied and showed intraepidermal pustular abscess with a neutrophilic infiltrate. Treatment commenced with intravenous fluids, antibiotics, systemic prednisone, steroid creams, and phototherapy(UVB) under the careful fetal well being monitoring. Cesarean section was done due to fetal distress, and a normal healthy male infant was delivered, following which the patient's condition improved rapidly.
Abscess
;
Anti-Bacterial Agents
;
Cesarean Section
;
Diagnostic Errors
;
Exanthema
;
Female
;
Fetal Distress
;
Fever
;
Humans
;
Impetigo*
;
Infant
;
Leukocytosis
;
Male
;
Neutrophils
;
Prednisone
;
Pregnancy*
;
Psoriasis
;
Skin
;
Thigh
8.Pulmonic stenosis with atrial septal defect in a Siamese cat.
Ji Youn KIM ; Sung Wook LEE ; Seung Gon LEE ; Sang Il SUH ; Changbaig HYUN
Korean Journal of Veterinary Research 2017;57(1):63-66
A 6-month-old mature intact female Siamese cat presented with exertional dyspnea. Diagnostic studies revealed pleural effusion, grade 4/6 left basal systolic murmur, deep S-wave in electrocardiograph leads I, II, and III, cardiomegaly with pleural effusion on radiography, pulmonic systolic (~5.8 m/sec) and tricuspid (3.6 m/sec) regurgitant jets, atrial septal defect, and a hypoplastic right outflow tract. Based on these results, the case was diagnosed as pulmonic stenosis with atrial septal defect. To the best of our knowledge, this is the first case report describing pulmonic stenosis with atrial septal defect in a cat in Korea.
Animals
;
Cardiomegaly
;
Cats*
;
Dyspnea
;
Electrocardiography
;
Female
;
Heart Defects, Congenital
;
Heart Septal Defects, Atrial*
;
Humans
;
Infant
;
Korea
;
Pleural Effusion
;
Pulmonary Valve Stenosis*
;
Radiography
;
Systolic Murmurs
9.A Case Report: Implantation of Balloon-Expandable Stent for Coarctation of the Aorta, Associated with Congenital Mitral Stenosis.
Seung Hyuk CHOI ; Sang Hak LEE ; Myeng Gon KIM ; Se Joong RIM ; Do Yun LEE ; Won Heum SHIM
Korean Circulation Journal 1998;28(5):819-824
Coarctation of aorta is a rare cause of secondary hypertension, and premature death will occur if no appropriate treatment is given. The only effective treatment was surgery before 1980, but restenosis was frequent. Several works on percutaneous transluminal angioplasty of the disease were reported. In patients with previously operated recoarctation, there is no doubt that balloon angioplasty is now the first choice of the therapy because of the surgical risks of reoperation. Nevertheless, there has still been some controversy regarding the application of this therapy to native coarctation, because of the potential risk of aortic disruption and the high incidence of restenosis. There have been some clinical reports of successful stent implantation for coarctation without major complications since 1991. We report on our experience with balloon-expandable stent implantation for native coarctation of the aorta in a 23-year-old man with congenital mitral stenosis. Aortogram showed a coarcted aortic segment of 3 mm in diameter and 25 mm long just distal to the left subclavian artery. The peak systolic pressure gradient across the coarctation before stent implantation was 100 mmHg. Stent implantation was performed with 14 X 40 mm balloon with Palmaz P308 stent. The peak systolic pressure gradient decreased to zero and the diameter of the coarctation of aorta increased to 14 mm after stent implantation immediately. The patient tolerated well and no significant complications were encountered during the procedure.
Angioplasty
;
Angioplasty, Balloon
;
Aortic Coarctation*
;
Blood Pressure
;
Humans
;
Hypertension
;
Incidence
;
Mitral Valve Stenosis*
;
Mortality, Premature
;
Reoperation
;
Stents*
;
Subclavian Artery
;
Young Adult
10.A Case Report: Implantation of Balloon-Expandable Stent for Coarctation of the Aorta, Associated with Congenital Mitral Stenosis.
Seung Hyuk CHOI ; Sang Hak LEE ; Myeng Gon KIM ; Se Joong RIM ; Do Yun LEE ; Won Heum SHIM
Korean Circulation Journal 1998;28(5):819-824
Coarctation of aorta is a rare cause of secondary hypertension, and premature death will occur if no appropriate treatment is given. The only effective treatment was surgery before 1980, but restenosis was frequent. Several works on percutaneous transluminal angioplasty of the disease were reported. In patients with previously operated recoarctation, there is no doubt that balloon angioplasty is now the first choice of the therapy because of the surgical risks of reoperation. Nevertheless, there has still been some controversy regarding the application of this therapy to native coarctation, because of the potential risk of aortic disruption and the high incidence of restenosis. There have been some clinical reports of successful stent implantation for coarctation without major complications since 1991. We report on our experience with balloon-expandable stent implantation for native coarctation of the aorta in a 23-year-old man with congenital mitral stenosis. Aortogram showed a coarcted aortic segment of 3 mm in diameter and 25 mm long just distal to the left subclavian artery. The peak systolic pressure gradient across the coarctation before stent implantation was 100 mmHg. Stent implantation was performed with 14 X 40 mm balloon with Palmaz P308 stent. The peak systolic pressure gradient decreased to zero and the diameter of the coarctation of aorta increased to 14 mm after stent implantation immediately. The patient tolerated well and no significant complications were encountered during the procedure.
Angioplasty
;
Angioplasty, Balloon
;
Aortic Coarctation*
;
Blood Pressure
;
Humans
;
Hypertension
;
Incidence
;
Mitral Valve Stenosis*
;
Mortality, Premature
;
Reoperation
;
Stents*
;
Subclavian Artery
;
Young Adult