2.Calcification and Aneurysms of Coronary Artery without Atherosclerosis in Young Adult.
Ji Shin LEE ; Young Jik LEE ; Jong Tae PARK
Korean Journal of Legal Medicine 1997;21(1):105-112
Coronary artery calcification(CAC) is found frequently in the atheromatous plaques CAC is known to have increased frequency above 40 years. CAC without evidence of atherosclerosis in young adults is quite rare, however, CAC combined with aneurysms in young adults have been infrequently reported in patients with a past history of a Kawasaki disease in child. We report an autopsy case showing CAC and aneurysm in the absence of macroscopically identified atherosclerotic lesions in a healthy 23-year-old man. The autopsy examination revealed aneurysmal dilatation of the right coronary artery which was connected with calcified lesion. A calcified lesion of the left anterior descending coronary artery was aslo noted. Microscopically, aneurysmal wall was non-specific except for hyalinized wall and foci of calcification. A striking histologic finding of calcified mass was ring calcification along the wall of the coronary artery. Antecedent Kawasaki disease in the past was suggestive as other reports.
Aneurysm*
;
Atherosclerosis*
;
Autopsy
;
Child
;
Coronary Vessels*
;
Dilatation
;
Humans
;
Hyalin
;
Mucocutaneous Lymph Node Syndrome
;
Plaque, Atherosclerotic
;
Strikes, Employee
;
Young Adult*
3.A Study for Hemodynamic Mechanism of Myocardial Infarction following Aortic Dissection.
Young Jik LEE ; Ji Shin LEE ; Jong Tae PARK
Korean Journal of Legal Medicine 1997;21(1):97-104
Aortic dissection may be considered the result of a discrepancy between the strength of the aortic wall and the intramural pressure. And factors that predispose to aortic dissection may include systemic hypertension, cystic medial necrosis, Marfan's syndrome, atherosclerosis, disease of aortic valve, pregnancy, giant cell arteritis, hyperthyrosis, disease of aortic valve, pregnancy, giant cell arteritis, hyperthyroidism, and blunt chest trauma. A few of aortic dissection may extend retrograde toward the aortic valve and involve the coronary arteries. Coronary artery occlusions due to mural dissection are an uncommon but well documented cause of myocardial infarction. Although rare, extramural hematoma compressing the coronary artery is another cause of myocardial infarction. At autopsy of 43 years old male who had no critical external wound, pericardial sac was distended and contained 400ml of dark red and clotted blood. Examination of the aorta revealed only minute atherosclerosis, intact aortic valve, and patent coronary ostia. 0.5cm sized aortic rupture was noted at the 3.5cm distal to the aortic valve. DeBakey type II aortic dissection was found to involve the ascending aorta and brachiocephalic trunk. Three intimal tears were 1.5cm, 8cm. 11.5cm distal to the aortic valve and two false lumens which had intact area between them extended 3.5cm distal to the third intimal tear and proximally in a retrograde fashion to the aortic root. Microscopically, sections of aorta showed relatively intact arrangement of smooth muscle and elastic fibers, except mild vascular ectasia and scattered several foci of the small sized aggregation of foamy histiocytes, and there was no evidence of cystic medial degeneration in aorta. Sections of both coronary arteries did not show mural dissection or atherosclerosis. Sections of right atrium and sinus node showed inflammatory reaction, extensive replacement of myocardium by active fibrous tissue consistent with infarction. There was no histologic evidence of myocardial infarction in the walls of other chambers or septum of the heart. We believe that extramural compression of the artery to sinus m\node by the dissecting hematoma was the cause of myocardial infarction involving the right atrium and the sinus node.
Adult
;
Aorta
;
Aortic Rupture
;
Aortic Valve
;
Arteries
;
Atherosclerosis
;
Autopsy
;
Brachiocephalic Trunk
;
Coronary Vessels
;
Dilatation, Pathologic
;
Elastic Tissue
;
Giant Cell Arteritis
;
Heart
;
Heart Atria
;
Hematoma
;
Hemodynamics*
;
Histiocytes
;
Humans
;
Hypertension
;
Hyperthyroidism
;
Infarction
;
Male
;
Marfan Syndrome
;
Muscle, Smooth
;
Myocardial Infarction*
;
Myocardium
;
Necrosis
;
Pregnancy
;
Sinoatrial Node
;
Thorax
;
Wounds and Injuries
4.Perinatal Prognosis of Single Umbilical Artery.
Yoon Ha KIM ; Tae Bok SONG ; Ji Soo BYUN ; Young Youn CHOI ; Ji Young LEE
Korean Journal of Perinatology 1999;10(2):155-160
OBJECTIVE: To evaluate the perinatal prognosis of fetuses with a single umbilical artery. METHODS: From 1992 to 1998, nineteen cases with single umbilical artery(SUA) was observed in 8,704 deliveries at Chonnam University Hospital. RESULTS: Out of nineteen fetuses, thirteen fetuses with single umbilical artery were detected by antenatal ultrasonographic examination and six fetuses were detected after birth. The male to female ratio was 0.9: 1. Congenital malformations were observed in 8 babies(42.1%) and included leg deformity, esophageal atresia, imperforated anus, ventriculomegaly, meningocele, hydronephrosis, ventricular septal defect, joint contracture, cleft lip and palate, toe anomaly, imperforated anus, kyphosis, no urethra and testis, clubfoot, patent ductus arteriosus and rnild mitral regurgitation. Among 10 cases of karyotyping analysis three cases were diagnosed as trisomy 18. Fourteen fetuses(77.8%) showed growth restriction at delivery. Antenatal obstetric complications were hydramnios(n = 3), oligohydramnios(n =2), and severe preeclampsia(n = 3). CONCLUSION: Careful ultrasonographic evaluation for the identification of a SUA is necessary because of its frequent association with congenital anomaly, growth restriction and cytogenetic abnormality.
Anal Canal
;
Chromosome Aberrations
;
Cleft Lip
;
Clubfoot
;
Congenital Abnormalities
;
Contracture
;
Ductus Arteriosus, Patent
;
Esophageal Atresia
;
Female
;
Fetus
;
Heart Septal Defects, Ventricular
;
Humans
;
Hydronephrosis
;
Jeollanam-do
;
Joints
;
Karyotyping
;
Kyphosis
;
Leg
;
Male
;
Meningocele
;
Mitral Valve Insufficiency
;
Palate
;
Parturition
;
Prognosis*
;
Single Umbilical Artery*
;
Testis
;
Toes
;
Trisomy
;
Urethra
5.Two Cases of Multicystic Encephalomalacia in a Surviving Co-twin with One Intrauterine Fetal Death.
Tae Bok SONG ; Young Youn CHOI ; Tae Hyung CHO ; Ji Sun KANG ; Chang Yee CHO
Korean Journal of Perinatology 1998;9(3):314-319
Various anatomical defects have been described in the surviving co-twin who had stillborn, macerated monozygotic co-twin with disseminated intravascular coagulation. The suggested mechanism was the transfer of emboli or thromboplastic materials of dead fetus to co-twin through placental vascular anastomoses. Multicystic encephalomalacia is the condition defined anatomically by the presence of multiple cavities in the great part of both cerebral hemispheres. The most common pathogenesis is circulatory disturbance caused by neonatal asphyxia during the perinatal period. We experienced two cases of monozygotic twin with deceased co-twin at 26 weeks, 33 weeks of gestation and confirmed the diffuse multicystic encephalomalacia by cranial ultrasonography and MRI in a surviving co-twin. Only one patient has been followed who showed spastic cerebral palsy and severe mental retardation. We report two cases of multicystic encephalomalacia in a surviring co-twin with a intrauterine fetal death and its related literatures.
Asphyxia
;
Cerebral Palsy
;
Cerebrum
;
Disseminated Intravascular Coagulation
;
Encephalomalacia*
;
Fetal Death*
;
Fetus
;
Humans
;
Intellectual Disability
;
Magnetic Resonance Imaging
;
Pregnancy
;
Pregnancy, Twin
;
Twins, Monozygotic
;
Ultrasonography
6.A Case of Solitary Eccrine Syringofibroadenoma on the Left Inframammary Area.
Young Jin KIM ; Hye Young LEE ; Ji Yeoun LEE ; Mi Kyeong KIM ; Tae Young YOON
Korean Journal of Dermatology 2012;50(12):1085-1087
No abstract available.
7.A Case of Verrucous Psoriasis.
Young Jin KIM ; Hye Young LEE ; Ji Yeoun LEE ; Mi Kyeong KIM ; Tae Young YOON
Korean Journal of Dermatology 2012;50(5):487-488
No abstract available.
Psoriasis
8.Changes of Thyroid Hormone during Open Heart Surgery.
Sung Jin HONG ; Young Tae KIM ; Ji Young LEE ; Se Ho MOON
Korean Journal of Anesthesiology 1997;33(1):122-126
BACKGROUND: The purpose of this prospective study is to define the effect of cardiopulmonary bypass (CPB) on the concentration of thyroid hormones and metabolites. METHODS: Blood samples were obtained from 15 patients undergoing open heart surgery at 1) pre-induction, 2) after heparinization, 3) during CPB, 4) 2 hours after CPB, 5) 24 hours after CPB and 6) 48 hours after CPB. Thyroid stimulating hormone, albumin, thyroxine (T4), free thyroxine (FT4), triiodothyronine (T3), free triiodothyronine (FT3) and reverse T3 (T3) were measured. RESULTS: Concentration of T3 significantly decreased after infusion of heparin and maintained at the decreased level until postbypass 24 hours. Concentration of FT3 significantly increased after heparin administration but maintained at a control level during CPB and decreased after postbypass 24 , 48 hours (p<0.05). Reverse T3 increased at 24 and 48 hours after CPB (p<0.05). Thyroxine decreased during CPB and return to control level after CPB. Free thyroxine did not change significantly. Thyroid stimulating hormone was significantly depressed at 24 hours after CPB (p<0.05). CONCLUSIONS: This result suggest that the thyroid function is depressed until 48 hours after CPB and it seems to be associated with abnormal metabolism of thyroid hormones.
Cardiopulmonary Bypass
;
Heart*
;
Heparin
;
Humans
;
Metabolism
;
Prospective Studies
;
Thoracic Surgery*
;
Thyroid Gland*
;
Thyroid Hormones
;
Thyrotropin
;
Thyroxine
;
Triiodothyronine
9.Familial Atrophoderma Vermiculata Associated with Epidermal Cysts.
Young Gi KIM ; June Woo KIM ; Mi Kyeong KIM ; Ji Yeoun LEE ; Tae Young YOON
Annals of Dermatology 2005;17(2):102-105
No abstract available.
Epidermal Cyst*
10.Trichothiodystrophy with Cerebral Hypomyelination.
Young Gi KIM ; June Woo KIM ; Il Hun BAE ; Ji Yeoun LEE ; Tae Young YOON
Annals of Dermatology 2005;17(2):98-101
No abstract available.
Trichothiodystrophy Syndromes*