1.Chest Pain.
Journal of the Korean Medical Association 2000;43(12):1219-1222
No abstract available.
Chest Pain*
;
Thorax*
2.Androgen, Lipid and Cardiovascular System.
Korean Journal of Andrology 1998;16(1):21-25
No abstract available.
Cardiovascular System*
3.Androgen, Lipid and Cardiovascular System.
Korean Journal of Andrology 1998;16(1):21-25
No abstract available.
Cardiovascular System*
4.Management of Male Osteoporosis.
Journal of the Korean Medical Association 1998;41(9):941-948
No abstract available.
Humans
;
Male*
;
Osteoporosis*
6.Urinary Incontinence.
Journal of the Korean Medical Association 1998;41(4):436-441
No abstract available.
Urinary Incontinence*
7.Embryogensis of Human Liver.
Korean Journal of Pathology 1990;24(4):393-401
The morphologic development of the liver in the embryonic period is described in serial sections of 18 human embryos representative of Horizons 12 to 23 . In the earliest specimen of horizon 12, the liver is seen as branching cord of endodermal cells originating from the hepatic diverticulum and invading into the loose stroma of septum transversum, transforming the surrounding stromal cells into primitive blood spaces and blood cells. Thereafter, the parenchymal cells rapidly proliferated so that the size of the organ was reaching a fifth of the CR length in horizon 23. The vascular system of the liver was in a symmetric configuration in horizon 12, which is composed of umbilical and vitelline veins and hepatocardiac channels on both sides. The evolution of the vascular system includes intergration of the vitelline veins into the portal vein, obliteration of the right umbilical vein and left hepatocardiac channel, and creation of the ductus venosus. The intrahepatic biliary tract is found to be formed by the "in situ transformation" mechanism, which involves transformation of the parenchymal cells, adjacent to the fibrous tissue surrounding the portal and umbilical veins, to networks of cuboidal epithelial cells lining the ductal lumen. These intrahepatic duct systems were found to communicate with the extrahepatic system at the porta hepatis.
Humans
8.Perianal Granuloma Caused by a Female Pinworm (Enterobius vermicularis): A case report.
Korean Journal of Pathology 2000;34(8):605-607
The intestinal nematode Enterobius vermicularis is the most common metazoan endoparasite in humans, with humans being the only host. But complicated perianal granulomas due to Enterobius are unusual. The literature reports only 13 previous cases of enterobiasis presenting as perianal mass or abscess. We describe an additional case of a perianal mass caused by granulomatous inflammation containing Enterobius vermicularis eggs and dead bodies in a 7-year-old boy. The lesion was located in the anus and measured 2 1 cm. Clinical impression was lipoma and excisional biopsy was done. Microscopic examination revealed necrotizing granuloma which contained several 50~60 20~30 micrometer sized eggs which were identified as those of Enterobius vermicularis. The adult worm could not be identified with clarity due to necrosis.
Abscess
;
Adult
;
Anal Canal
;
Biopsy
;
Child
;
Eggs
;
Enterobiasis
;
Enterobius*
;
Female*
;
Granuloma*
;
Humans
;
Inflammation
;
Lipoma
;
Male
;
Necrosis
;
Ovum
9.Laryngeal Atresia with Tracheoesophageal Fistula: 1 case report.
Korean Journal of Pathology 1993;27(5):504-508
Laryngeal atresia is a very rare congenital anomaly requiring immediate tracheotomy. We present a case of laryngeal atresia with tracheoesophageal fistula who showed immediate respiratory difficulty after ligation of umbilical cord and died of aspiration pneumonia at 8 days of age. The atretic portion of larynx is composed of irregulary arranged cartilaginous tissue, bundles of intrinsic muscle and soft tissue without epithelium-lined lumen. The lungs show normal development and evidences of aspiration pneumonia.
Infant, Newborn
;
Humans
10.Nasal Cerebral Heterotopia-so called Nasal Glioma: A case report.
Korean Journal of Pathology 1995;29(4):517-520
Encephalocele and nasal glioma are rare, benign congenital neuroectodennal tumors which result from a failure of embryologic sepearation of neuroectodermal and ectodemlal tissues. Nasal glioma should be differentiated from a true glioma, and from a primary encephalocele, which is a herniation of the cranial contents through a bony defect in the skull. For this reason, nasal cerebral heterotopia is a preferred term. We report an unusual case of a nasal mass that was histologically indistinguishable from nasal cerebral heterotopia but proved to be connected to the skull base by fibrotic cord. The patient was a 2 year old girl who had had a slow growing palpable mass in the left epicanthal area for three months.