1.Chronic Fatigue Syndrome.
Korean Journal of Medicine 2006;70(4):469-473
No abstract available.
Fatigue Syndrome, Chronic*
;
Fibromyalgia
2.Treatment of Congenital Dislocation of Hip in Children Under the Age of 2 Years
Sung Man ROWE ; Il Sung PARK ; Ju Chull CHUNG
The Journal of the Korean Orthopaedic Association 1990;25(5):1478-1486
The authors report a clinical experience of 95 patients (98 hips) with congenital dislocation of hip under the age of 2 years who were followed up at least 1 year at Chonnam University Hospital between 1979 and 1988. The result of clinical analysis are as follows; 1. The most patients were girls, comprising 87 girls (89 hips) and 8 boys (9 hips). 2. The age at treatment were under the age of 6 months in 49 hips, 7 to 12 months in 5, 13 to 18 months in 30 and 19 to 24 months in 14. 3. The initial treatment of the 98 hips were Pavlik harness in 49 hips, closed reduction in 18, and open reduction in 31. 4. Pavlik harness was applied to the patients under the age of 7 months and the results were acceptable in 37 hips (76%), uncertain in 4 (8%) and unacceptable in 8 (16%). The 8 unacceptable hips were retreated by closed reduction in 6 hips and open reduction in 2. 5. Closed reduction was applied to the patients ranging from the age of 4 months to 21 months and the results were acceptable in 14 hips(78%), unacceptable in 4 (22%). The 4 unacceptable hips were retreated by open reduction in 3 hips and Salter innominate osteotomy in l. 6. Open reduction was applied to the patients ranging from the age of 7 months to 20 months, and the results were acceptable in 26 hips (84%), uncertain in 3 (10%) and unacceptable in 2 (6%). The one of 2 unacceptable hips was retreated by Salter innominate osteotomy. 7. The overall results of 98 hips following initial treatment were acceptable in 77 hips (79%), uncertain in 7 (7%), and unacceptable in 14 (14%). The final results after secondary treatment were acceptable in 89 hips (91%), uncertain in 7 (7%), and unacceptable in 2 (2%).
Child
;
Dislocations
;
Female
;
Hip
;
Humans
;
Jeollanam-do
;
Osteotomy
3.A case of cerebro-oculo-facio-skeletal syndrome.
Sung Shin PARK ; Ju Seok MAENG ; Jae Ok PARK
Journal of the Korean Pediatric Society 1991;34(11):1593-1597
No abstract available.
4.Classification of the Site of Ventricular Septal Defect with 2-Dimensional Doppler Echocardiography.
Yung Woo SHIN ; Hee Ju PARK ; Si Chan SUNG
Korean Circulation Journal 1990;20(1):11-18
One hundred seven consecutive patients aged 3 years to 34 years with simple ventricular septal defect were prospectively investigated with 2-dimensional Doppler echocardiography to assess the echocardiographic criteriae in defining the anatomic site of the VSD. The anatomy was confirmed in all patients at operation. Two-dimensional Doppler echocardiography correctly categorized the site and extension of VSDs in 104 of 107(97%). All doubly committed subarterial VSDs were correctly diagnosed as an area of discontinuity beneath the pulmonary valve in the parasternal short-axis plane taken at the aortic root level. Forty eight of 49 perimembranous VSDs with infundibular extension showed an area of discontinuity beneath the right aortic cusp in the parasternal long axis plane of the left ventricle. Of 17 perimembranous VSDs with trabecular extension, 16 had an area of discontinuity around the medial papillary muscle in the short axis plane taken at the level of high left ventricular outflow tract(LVOT). All 5 perimembranous VSDs with inlet extension showed an area of discontinuity adjacent to the septal leaflet attachment in the short axis plane taken at the level of high LVOT. One muscular trabecular VSD was categorized correctly by the short axis view and the apical 4-chamber view. Thus, these 2-dimensional Doppler echocardiographic criteriae are a simple and reliable in identifying the anatomic site of VSDs.
Axis, Cervical Vertebra
;
Bays
;
Classification*
;
Echocardiography
;
Echocardiography, Doppler*
;
Heart Septal Defects, Ventricular*
;
Heart Ventricles
;
Humans
;
Papillary Muscles
;
Prospective Studies
;
Pulmonary Valve
5.The Use of Extracorporeal Membrane Oxygenation in the Surgical Repair of Bronchial Rupture.
Ju Hee PARK ; Junghyeon LIM ; Jaejin LEE ; Hee Sung LEE
Korean Journal of Critical Care Medicine 2016;31(1):54-57
Extracorporeal membrane oxygenation (ECMO) has been used successfully in critically ill patients with traumatic lung injury and offers an additional treatment modality. ECMO is mainly used as a bridge treatment to delayed surgical management; however, only a few case reports have presented the successful application of ECMO as intraoperative support during the surgical repair of traumatic bronchial injury. A 38-year-old man visited our hospital after a blunt chest trauma. His chest imaging showed hemopneumothorax in the left hemithorax and a finding suspicious for left main bronchus rupture. Bronchoscopy was performed and confirmed a tear in the left main bronchus and a congenital tracheal bronchus. We decided to provide venovenous ECMO support during surgery for bronchial repair. We successfully performed main bronchial repair in this traumatic patient with a congenital tracheal bronchus. We suggest that venovenous ECMO offers a good option for the treatment of bronchial rupture when adequate ventilation is not possible.
Adult
;
Bronchi
;
Bronchoscopy
;
Critical Illness
;
Extracorporeal Membrane Oxygenation*
;
Hemopneumothorax
;
Humans
;
Lung Injury
;
Rupture*
;
Tears
;
Thorax
;
Ventilation
;
Wounds, Nonpenetrating
6.A Case of Acute Generalized Exanthematous Pustulosis.
Sang Ju LEE ; Sung Nam CHANG ; Wook Hwa PARK
Korean Journal of Dermatology 1998;36(1):125-128
Acute generalized exanthematous pustulosis(AGEP) is a disease entity caused mostly by drugs or viral infections. Clinically it manifests as generalized erythema, erythema multiforme and amicrobial pustules with fever. Histologically, AGEP is composed of neutrophilic subcorneal and spongiform pustules. A 70-year-old female, with no personal or family history of psoriasis, was given medication including diltiazem for hypertension. Fourteen days after taking the medications, pustular eruptions appeared on the face and rapidly spread to the trunk and limbs. A Laboratory examination revealed neutrophilic leukocytosis and an elevated erythrocyte sedimentation rate. The skin biopsy showed subcorneal and spongiform pustules. We report here a case of AGEP probably due to diltiazem.
Acute Generalized Exanthematous Pustulosis*
;
Aged
;
Biopsy
;
Blood Sedimentation
;
Diltiazem
;
Erythema
;
Erythema Multiforme
;
Extremities
;
Female
;
Fever
;
Humans
;
Hypertension
;
Leukocytosis
;
Neutrophils
;
Psoriasis
;
Skin
7.The Wolf-Hirschhorn Syndrome in Fetal Autopsy: A Case Report.
Sun Ju BYEON ; Jae Kyung MYUNG ; Sung Hye PARK
Korean Journal of Pathology 2011;45(Suppl 1):S15-S19
Wolf-Hirschhorn syndrome (WHS) is a malformation associated with a hemizygous deletion of the distal short arm of chromosome 4. Herein we report a fetal autopsy case of WHS. A male fetus was therapeutically aborted at 17(+0) weeks gestational age, due to complex anomaly and intrauterine growth retardation, which were found in prenatal ultrasonography. His birth weight was 65 g. Mild craniofacial dysmorphism, club feet, bilateral renal hypoplasia, edematous neck, and left diaphragmatic hernia of Bochdalek were found on gross examination. On GTG-banding, the fetus revealed 46,XY,add(4p) karyotype and the mother revealed 46,XX,t(4;18)(p16;q21.1), with normal karyotype of the father. Array comparative genomic hybridization performed on the autopsied lung tissue revealed loss of 4p16.2-->4pter and gain of 18q21.1-->18qter, suggesting 46,XY,der(4)t(4;18)(p16.2;q21.1)mat of fetal karyotype. This suggested deletion of 4p, compatible with WHS inherited from the mal-segregation of a maternal translocation t(4;18)(p16.2;21.1). Therefore, our fetus was both genotypically and phenotypically compatible with WHS.
Arm
;
Autopsy
;
Birth Weight
;
Chromosomes, Human, Pair 4
;
Comparative Genomic Hybridization
;
Fathers
;
Fetal Growth Retardation
;
Fetus
;
Foot
;
Gestational Age
;
Hernia, Diaphragmatic
;
Humans
;
Karyotype
;
Karyotyping
;
Lung
;
Male
;
Mothers
;
Neck
;
Ultrasonography, Prenatal
;
Wolf-Hirschhorn Syndrome
8.Overview of Clinical Experience in the Treatment of Peptic Ulcer with Famotidine.
Choong Kee PARK ; Sang Un JU ; Kyu Sung RIM
Korean Journal of Gastrointestinal Endoscopy 1987;7(1):27-30
The aim of the investigation was to study the efficacy and safety of Famotidine (Gaster), a new, potent, histamine H-receptor antagonist. The Famotidine (40 mg p.o.h.s) was administered to 22 patients with 33 peptic ulcers for 4 weeks. Follow up checking was done at 2 week and 4 week by endoscopy and physical examination. All patients were carefully evaluated at regular intervals for adverse drugh reactions by clinical and laboratory examinations. By the end of study, 97% of the ulcers were healed by endoscopically and rapid and complete relief of epigastric pain was observed in all patients. Famotidine treatment was well tolerated and no alterations in laboratory tests were noted. Therfore, Famotidine was proved effective in the treatment of peptic ulcers (especially multiple ulcers) and was well tolerted on the short-term basis.
Endoscopy
;
Famotidine*
;
Follow-Up Studies
;
Histamine
;
Humans
;
Peptic Ulcer*
;
Physical Examination
;
Ulcer
9.On Reconstion with Bone Graft of the Defect of Radus: Report of 2 Cases
Sung Man ROWE ; Hun Soo PARK ; Suck Ju KOH
The Journal of the Korean Orthopaedic Association 1976;11(3):522-524
Defect of the radius should be managed with either fusion of radius and ulna forming “one-bone forearm”, or restoration of its continuity by bone graft. Reported hereia are two cases in which the radius developed defect following sequestrectomy and treatment of open infected fructure respectively. Reconstruction of the radius was tried with bone graft; utilizing the ulnar end resected from the same side in one case and fibula in other. Both Sowed sound bony union of the graft about four months postoperatively.
Fibula
;
Radius
;
Transplants
;
Ulna
10.Rhabdomyosarcoma of the Lower Leg in Newborn
Chong Il YOO ; Ju Ho SONG ; Sung Hae PARK
The Journal of the Korean Orthopaedic Association 1984;19(3):603-606
Rhabdomyosarcoma which was first described by Weber has generally been considered an uncommon tumor of striated muscle. Recently it was classified as four types as embryonal, alveolar, pleomorphic, and botryoid type by Horn and Enterline. A fourth type, sarcoma botryoides was generally recognized as a variant of the embryonal type. Al1 of these tumors tend to have a short clinical course, but the survival time seems to be slightly improved by sugical excision followed by radiotherapy and chemotherapy. Authors report one case of rhabdomyosarcoma, which was seen in the right lower leg and showed a rapid growing nature to die, which experienced in Busan National University Hospital, February, 1983.
Animals
;
Busan
;
Drug Therapy
;
Horns
;
Humans
;
Infant, Newborn
;
Leg
;
Muscle, Striated
;
Radiotherapy
;
Rhabdomyosarcoma
;
Rhabdomyosarcoma, Embryonal
;
Sarcoma