1.Congenital Cystic Adenomatoid Malformation of the Lung: Clinicopathologic analysis of 22 cases.
Young Lyun OH ; Yeon Lim SUH ; Je G CHI
Korean Journal of Pathology 1994;28(3):219-227
Congenital cystic adenomatoid malformation of the lung(CCAML) is a rare developmental anomaly characterized by an "adenomatoid" hyperplasia of terminal respiratory structures with formation of the cysts of varying sizes. CCAML is separated into three major types based on the gross and microscopic findings. We have analyzed 22 cases of CCAML, those consisted of 6 autopsy cases and 16 surgical specimens. Out of 22 cases, 5 cases were composed of large cysts(type I) and 9 cases had multiple small cysts(type II). Remaining one case revealed features of solid type(type III), and 7 cases were mixed form. There were 16 boys and 6 girls. All cases were below the age of 14 years. There was no clear-cut age difference between different types of CCAML. However, inflammation, fibrosis and pseudostratification of epithelium were often found in older age. All fetal autopsy cases of CCAML had hydrops fetalis and were associated with maternal hydramnios. One case of type III showed definite mucinogenic cells in the cysts unexpectedly, and one case of the mixed form(typeI+II+III) was found in a fetus of 22 weeks of gestational age. Above findings contradicted the classical description of the CCAML, and suggested that arbitrary classification into three types may not be the best way in understanding this condition.
Cysts
2.Fibrocalcific Nodule in the Liver Capsule Caused by Ascaris Eggs: A case report.
Yeon Lim SUH ; So Young PARK ; Je G CHI
Korean Journal of Pathology 1992;26(4):411-413
Ascariasis is probably the most common helminthic infestation of man, but it seldom causes severe illness. Pathologic conditions of Ascaris may be caused by adult worms, eggs or larvae. We describe a case of Ascaris egg granulomas that were found incidentally on the surface of the liver in a 75-year-old woman who had undergone a segmentectomy for an intrahepatic stone. Grossly, there were several yellowish calcific nodules of 0.4 cm in diameter on the lateral surface of the left lobe of the liver. Microscopically, the lesions were located in the hepatic capsule and consisted of fibrocalific nodules with many eggs. The eggs were round to oval, thick-shelled and measured 50~75x30~50 um. Most of the morphologically preserved eggs were fertilized eggs, but they had smooth shells without external protein coats. This case is of interest for the unusual location of the lesion, the presence of eggs without mammillation, and the association with the intrahepatic stone.
Adult
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Male
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Female
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Humans
3.Ultrasound screening for small hepatomas : A prospective study
Jae Hoon LIM ; Young Tae KO ; Chi Yul AHN ; Young Il MIN ; Hoong Zae ZOO
Journal of the Korean Radiological Society 1986;22(4):511-517
Small hepatoma is defined as hepatocellular carcinoma less than 3cm in maximum diameter and fewer than 3 innumber. To assess the ability of ultrasound to detect small hepatomas, a prospectively study was done in a groupof patients with HBsAg-positive chronic hepatitis and liver cirrhosis. Herein, we present 4 hypoechoic smallhepatomas detected on ultrasound and emphasize the role of real-time ultrasonography as a practical test formonitoring hepatoma high-risk, subjects.
Carcinoma, Hepatocellular
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Hepatitis, Chronic
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Humans
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Liver Cirrhosis
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Mass Screening
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Prospective Studies
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Ultrasonography
4.Neonatal Giant Cell Hepatitis: An autopsy case.
Sung Churl LIM ; Moo Young SONG ; Un Jun HYUNG ; Je G CHI
Korean Journal of Pathology 1991;25(2):147-152
We report an autopsy case of neonatal giant cell hepatitis that was presumed to be related to bacterial sepsis, endotoxemia and to the subsequent parenteral alimentation and antibiotics treatment. The patient died of candidal endocarditis and multiple brain infarcts. This female baby was born by a normal full term spontaneous delivery. Six days after delivery she developed fever and lethargy as she suffered from Cheyne-Stokes respiration with severe grunting. Blood culture grew Enterobacter and Acinetobacter. After management of the sepsis her general condition improved. On the 23rd day of admission she was found to have deep jaundice and hepatosplenomegaly. The liver became larger progressively and the edge was palpable at the umbilical level. Grade II systolic murmur was heard along the left lower sternal border. She died on the 31st day of hospitalization. Postmortem examination showed severe jaundice, hepatosplenomegaly, a large vegetation on the mitral valve and multiple petechial hemorrhages of the viscera. Microscopically the liver showed features of massive giant cell transformation, mild fibrosis and inflammatory cells, suggestive of giant cell hepatitis. Numerous yeasts and candidal pseudohyphae were seen in the cardiac vegetation, focally extending into the myocardium. There was a focus of candidal vasculitis in the bowel wall. In addition there were multiple bilateral organizing infarcts in the cerebral hemisphere as well as diffuse white matter damage associated with septicemia.
Female
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Infant, Newborn
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Humans
5.Cerebral Amyloid Angiopathy: A report of two cases.
Kee Taek JANG ; Ghee Young CHOE ; Yeon Lim SUH ; Je Geun CHI
Korean Journal of Pathology 1999;33(9):741-744
Cerebral amyloid angiopathy (C.A.A) is characterized by the extracellular amyloid protein deposition in the vessel walls of the brain and meninges. It has been estimated to account for 5 to 10% of all primary, nontraumatic brain hemorrhage. We report two cases of C.A.A causing nontraumatic intracerebral hemorrhage in the frontal lobe. The first case was a 60-year-old female who was admitted for the left hemiplegia and dysarthralgia. Brain CT revealed right frontal lobe hemorrhage. The second case was a 72-year-old male who was admitted for amnesia and gait disturbance. Clinical impression was Alzheimer's disease. Brain MRI revealed multifocal small hemorrhage in the right frontal lobe. Microscopically, both cases showed dilated small arteries of superficial cortex and meninges with hyalinization. Some vessels showed microaneurysm and fibriniod necrosis. Congo-red stain also exhibited birefringence under polarized light. There was no evidence of Alzheimer's disease.
Aged
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Alzheimer Disease
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Amnesia
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Amyloid
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Arteries
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Birefringence
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Brain
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Cerebral Amyloid Angiopathy*
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Cerebral Hemorrhage
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Female
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Frontal Lobe
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Gait
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Hemiplegia
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Hemorrhage
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Humans
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Hyalin
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Intracranial Hemorrhages
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Magnetic Resonance Imaging
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Male
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Meninges
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Middle Aged
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Necrosis
6.A Case of Wernicke's Encephalopathy Caused by Hyperemesis Gravidarum Complicated with Thyroid Storm and Abnormal Liver Function.
Sang In CHOI ; Chul Soo LIM ; Chi Young MOON ; Hong Sun BAEK
Journal of Korean Society of Endocrinology 1998;13(2):247-251
A 27-year-old woman developed Wemicke's encephalopathy in the 16th week of her first pregnaney. She had thyroid storm and abnormal liver function. Her thyrotoxic symptom and abncemal liver function was recovered after medication of antithyroid drug, steroid, hepatotonic drug and administration of thiamine(fursulthiamin), but the fetus was lost, Thereafter her thyroid function returned to normal and euthyroid state was maintained without medication of antithyroid drug, but her neurological defect was remained. We suggest that severe hyperemesis gravidarum is a possible risk factor of the thyroid storm and Wemicke's encephalopathy in patients with hyperthyroidism, and consider the check of the thyroid function. The need for parenteral thiamine supplementation and medication of antithyroid drug is warranted in patients with severe hyperemesis gravidarum which lasts longer than 3 weeks and abnormal thyroid function.
Adult
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Female
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Fetus
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Humans
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Hyperemesis Gravidarum*
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Hyperthyroidism
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Liver*
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Pregnancy
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Risk Factors
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Thiamine
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Thyroid Crisis*
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Thyroid Gland*
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Wernicke Encephalopathy*
7.Sturge-Weber Syndrome: Report of an incomplete form.
Hye Yeon KIM ; Kap No LEE ; Seung Young PAIK ; Ki Chan LEE ; Chang Soo LIM ; Suck Ho NAM ; Je G CHI
Korean Journal of Pathology 1985;19(2):226-230
The Sturge Weber syndrome is an uncommon disorder characterized by port-wine nevus of the face with angiomatosis of the ipsilateral cerebral leptomeninges and extensive calcification in the underlying cerebral cortex. Associated with this syndrome are mental retardation, choroidal angioma, buphthalmus or glaucoma, seizure and hemiplegia. We studied a case of incomplete form of Sturage Weber syndrome in a 12 year-old boy, who had generalized seizure, a homonymous hemianopsia, intracranial calcification and leptomeningeal angiomatosis. There are no characteristic facial nevus, mental retardation, occular changes and hemiplegia.
8.Population-Based Study of the Epidemiology of Herpes Zoster in Korea.
You Jeong KIM ; Chang Nam LEE ; Chi Yeon LIM ; Woo Seok JEON ; Young Min PARK
Journal of Korean Medical Science 2014;29(12):1706-1710
General epidemiological data regarding herpes zoster (HZ) are necessary for treatment and prevention of this disease. In addition, epidemiological data can play an important role in evaluating the efficacy and impact of vaccination. Though several epidemiological studies of HZ in Korea have been conducted, they usually depend on hospital-based data and may not be representative of HZ characteristics all over Korea. The purpose of this study was to evaluate the incidence and other epidemiological features of HZ in the general Korean population. We used population-based medical records from the Health Insurance Review & Assessment Service, which includes 50,908,646 medical insurance subscribers, to calculate the incidence of HZ. Also, we analyzed an age-stratified random sample of 1,375,842 individuals to study descriptive epidemiologic characteristics of HZ in Korea in 2011. We observed that the incidence of HZ was 10.4 per 1,000 person-years and was strongly correlated with age. Sex had a major influence on HZ incidence; overall, there were 12.6 cases per 1,000 person years in women and 8.3 cases per 1,000 person years in men. There was no difference in incidence according to the locality and season.
Adolescent
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Adult
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Age Distribution
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Aged
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Aged, 80 and over
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Child
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Child, Preschool
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Female
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Herpes Zoster/*diagnosis/*epidemiology
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Hospitalization/*statistics & numerical data
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Humans
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Infant
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Infant, Newborn
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Male
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Middle Aged
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Prevalence
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Republic of Korea/epidemiology
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Risk Factors
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Seasons
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Sex Distribution
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Young Adult
9.Peritoneal Metastasis of an Carcinoma in the Appendix.
Chi Young LIM ; Jong Woo KIM ; Seung Ki KIM ; Kyong Po LEE
Journal of the Korean Society of Coloproctology 2004;20(6):411-414
An adenocarcinoma of the appendix is a rare tumor, and so far only 130 cases have been reported worldwide. We report one patient with peritoneal seeding of an adenocarcinoma. A 51-year-old man was admitted to our hospital with the impression of intestinal obstruction. He had undergone an appendectomy 5 years ago due to acute appendicitis. At that time, postoperative histopathological analysis had revealed an adenocarcinoid tumor in the appendix. The patient had been told to visit our hospital for follow-up but he hadn't visited. When he finally visited our hospital diagnostic laparoscopy revealed the peritoneal seeding of a recurrent adenocarcinoma. A palliative right hemicolectomy was done to relieve the bowel obstruction. After recovering from operation, the patient was treated with the 5-fluoruracil, leucovorin, and oxaloplatin (FOLFOX). The patient was discharged in improved general condition with a future plan for regular cyclic chemotherapy.
Adenocarcinoma
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Appendectomy
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Appendicitis
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Appendix*
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Carcinoid Tumor
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Drug Therapy
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Follow-Up Studies
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Humans
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Intestinal Obstruction
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Laparoscopy
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Leucovorin
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Middle Aged
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Neoplasm Metastasis*
10.No title available in English.
Whan Nam KANG ; Kee Hyun NAM ; Chi Young LIM ; Hang Seok CHANG ; Cheong Soo PARK ; Jan Dee LEE
Korean Journal of Endocrine Surgery 2005;5(1):43-45
No abstract available.