1.Thyroid Tumor and Oncogene.
Journal of Korean Society of Endocrinology 1998;13(2):145-149
No abstract available.
Oncogenes*
;
Thyroid Gland*
2.Prevalence and risk factors of the osteoporosis of perimenopausal women.
Korean Journal of Medicine 2002;62(1):1-3
No abstract available.
Female
;
Humans
;
Osteoporosis*
;
Prevalence*
;
Risk Factors*
3.2013 Preface: On the Occasion of Publishing the Endocrinology and Metabolism in English.
Endocrinology and Metabolism 2013;28(1):1-2
No abstract available.
Endocrinology
4.Calcitropic Hormones and Systemic Factors of Vascular Calcification.
Journal of Korean Society of Endocrinology 2005;20(6):561-570
No Abstract available.
Vascular Calcification*
5.Sebaceous Trichofolliculoma: A case report.
Jeana KIM ; Seong Beom LEE ; Seok Jin KANG ; Soo Il CHUNG ; Sun Moo KIM
Korean Journal of Pathology 1995;29(6):794-796
Sebaceous trichofolliculoma is a variant of trichofolliculoma which occurs in the sebaceous areas rich in follicles and is a relatively rare skin tumor. This tumor is a clinically and histologically easy tumor to recognize that is well differentiated. We examined a case of a consists of a 21-year-old female who had a pedunculated nodule on her scalp. Microscopically, the tumor was large, had a centrally located cavity lined by squamous epithelium and radially arranged sebaceous follicles connected to the cavity. No cytological atypia or recurrence after excision was found.
Female
;
Humans
6.Solitary Fibrofolliculoma: A case report.
Hun Kyung LEE ; Lee So MAENG ; Seok Jin KANG ; Soo Il CHUNG ; Sun Moo KIM
Korean Journal of Pathology 1996;30(5):460-462
The clinical and pathological features of solitary fibrofolliculoma are presented. Solitary fibrofolliculoma is very rarely encountered and to our knowledge, only 7 cases have been reported in the Western literature and no cases have been published in Korea. We experienced a case of solitary fibrofolliculoma occurring in a 56-year-old female, who had a 1.0 cm-sized and slowly growing nodule on her chin. A brief review of the literature, was made especially in relation to the pathological findings and histogenesis of solitary fibrofolliculoma.
Female
;
Humans
7.Official Positions of the International Society for Clinical Densitometry.
Journal of Korean Society of Endocrinology 2005;20(1):1-7
No abstract available.
Densitometry*
8.Primary Malignant Lymphoma of the Liver: Report of a case.
Soo Kyong CHUNG ; Chang Suck KANG ; Won Il KIM ; Sang In SHIM ; Sun Moo KIM
Korean Journal of Pathology 1987;21(4):285-290
Primary extranodal lymphoma of the liver is very rare, approximately thirty-one cases having been reported in the literature. We report one case of primary malignant lymphoma of the liver in a 26-year-old female, who was presented with palpable abdominal mass on the epigastrium for about 40 days. Laboratory findings revealed no specific abnormalities. Peripheral lymph nodes or spleen were not palpable. An abdominal ultrasonogram revealed a huge mass involving the entire left lobe of the liver. Left lateral segmentectomy of the liver was done. The resected lateral portion of left lobe of the liver showed a large solitary mass, 12 cm in the greatest dimension, with a yellowish gray fleshy solid cut surface. Though light microscopic feature was compatible with primary malignant lymphoma, diffuse large cell type, intermediate grade by the working formulation, undifferentiated carcinomas including hepatocellular carcinoma, plasmacytoma, and pleomorphic sarcomas could not be completely ruled out. Thus, marker studies and electron microscopic examination were performed. Immunoperoxidase stains for common leukocyte antigen was positive, and the Leder stain for myeloid granule was negative. Electron microscopic stuids revealed findings of neoplastic lymphoid cells, consistent with malignant lymphoma. Primary lymphoma of the liver has only rarely been reported, and its natural history is unclear. Many of the reported cases have been large cell lymphomas, as in this case.
Female
;
Humans
;
Carcinoma, Hepatocellular
9.Effect of Lidocaine and Ketamine Pretreatment on Vascular Pain Associated with Intravenous Propofol Injection.
Wha Ja KANG ; Dong Gun LEE ; Dong Ok KIM ; Moo Il KWON ; Dong Soo KIM ; Kwang Il SHIN
Korean Journal of Anesthesiology 1997;33(4):716-720
BACKGROUND: Propofol has a high incidence of pain with intravenous injection, and different methods have been used to minimize the incidence and severity of this pain. In this study, we have compared the effect of lidocaine pretreatment with that of ketamine pretreatment on propofol injection pain. METHODS: Ninety healthy female patients scheduled for general anesthesia were randomly divided into three groups; saline group (n=30), lidocaine group (n=30) and ketamine group (n=30). Each patient received 2 ml of pretreatment solution (normal saline, 1% lidocaine, 0.5% ketamine) via 18G angiocatheter inserted in the antecubital fossa after applying an arm tourniquet inflated to 50 mmHg. The tourniquet was released 1 minute later, followed by intravenous injection of 2.5 mg/kg of propofol. The assessment of pain was made at the induction of anesthesia and in the recovery room, and the severity of pain was classified as none, mild, moderate, severe by one observer. RESULTS: The severity and incidence of pain diminished significantly in the lidocaine group and the ketamine group compared with the saline group at the induction of anesthesia (p<0.05) and there was no significant difference between the lidocaine group and the ketamine group. We had similar results in the recovery room and one patient from the saline group and the ketamine group had no recall regarding injection pain. CONCLUSION: Intravenous ketamine pretreatment is as effective as intravenous lidocaine pretreatment in alleviating the propofol injection pain.
Anesthesia
;
Anesthesia, General
;
Arm
;
Female
;
Humans
;
Incidence
;
Injections, Intravenous
;
Ketamine*
;
Lidocaine*
;
Propofol*
;
Recovery Room
;
Tourniquets
10.A Case of Normalized Hypertrophic Cardiomyopathy after Removal of Pheochromocytoma.
Moo Il KANG ; Chong Heung OH ; Jang Seong CHAE ; Jae Hyung KIM ; Soon Jo HONG ; Kyu Bo CHOI ; Hak Joong KIM ; Sun Moo KIM
Korean Circulation Journal 1988;18(2):299-306
The characterisitic finding of hypertrophic cardiomyopathy is left ventricular hypertrophy without dilated chamber. Echocardiographic studies of patients with pheochromocytoma in the past have revealed both dilated and hypertrophic cardiomyopathies, as well as obstruction of the left ventricular outflow tract. We report this case because we experienced a pheochromocytoma patient who had reversible hypertrophic cardiomyopathy which might be related with circulating catecholamine level.
Cardiomyopathy, Hypertrophic*
;
Echocardiography
;
Humans
;
Hypertrophy, Left Ventricular
;
Pheochromocytoma*