1.A case of Hypokalemic Familial Periodic Paralysis.
Seong Kuk SEO ; Gyu Ha LEE ; Han Young JEONG ; Sung Won KIM ; Kil Hyun KIM
Journal of the Korean Pediatric Society 1989;32(7):1012-1016
No abstract available.
Paralyses, Familial Periodic*
2.A Case of Hydrops Fetalis due to Rh-Incompatibility.
Seong Kuk SEO ; Han Young JEONG ; Sung Won KIM ; Kil Hyun KIM
Journal of the Korean Pediatric Society 1989;32(2):256-261
No abstract available.
Edema*
;
Hydrops Fetalis*
3.A Case of Hydrops Fetalis due to Rh-Incompatibility.
Seong Kuk SEO ; Han Young JEONG ; Sung Won KIM ; Kil Hyun KIM
Journal of the Korean Pediatric Society 1989;32(2):256-261
No abstract available.
Edema*
;
Hydrops Fetalis*
4.A Case of Central Dysplasia.
Seong Kuk SEO ; In Sook KIM ; Soon Yol HWANG ; Han Young JEONG ; Sung Won KIM ; Kil Hyun KIM
Journal of the Korean Pediatric Society 1989;32(2):276-279
No abstract available.
5.A Case of Central Dysplasia.
Seong Kuk SEO ; In Sook KIM ; Soon Yol HWANG ; Han Young JEONG ; Sung Won KIM ; Kil Hyun KIM
Journal of the Korean Pediatric Society 1989;32(2):276-279
No abstract available.
6.Urothelial Carcinoma of the Renal Pelvis with Synchronous Ipsilateral Collecting Duct Carcinoma:Two Case Reports
Sang Bin BAE ; Seong Kuk YOON ; Seo-hee RHA
Journal of the Korean Society of Radiology 2024;85(1):222-229
Synchronous renal malignancies are seldom encountered or diagnosed post-renal resection. A combination of renal cell carcinoma (RCC) and urothelial carcinoma (UC) is most commonly reported.Typically, the RCC subtype is clear-cell RCC; however, a combination of collecting duct carcinoma (CDC) and UC has rarely been reported in the existing literature. Here, we present two cases of synchronous renal malignancy, specifically a combination of CDC and UC, in the ipsilateral kidney.
7.Urothelial Carcinoma of the Renal Pelvis with Synchronous Ipsilateral Collecting Duct Carcinoma:Two Case Reports
Sang Bin BAE ; Seong Kuk YOON ; Seo-hee RHA
Journal of the Korean Society of Radiology 2024;85(1):222-229
Synchronous renal malignancies are seldom encountered or diagnosed post-renal resection. A combination of renal cell carcinoma (RCC) and urothelial carcinoma (UC) is most commonly reported.Typically, the RCC subtype is clear-cell RCC; however, a combination of collecting duct carcinoma (CDC) and UC has rarely been reported in the existing literature. Here, we present two cases of synchronous renal malignancy, specifically a combination of CDC and UC, in the ipsilateral kidney.
8.Urothelial Carcinoma of the Renal Pelvis with Synchronous Ipsilateral Collecting Duct Carcinoma:Two Case Reports
Sang Bin BAE ; Seong Kuk YOON ; Seo-hee RHA
Journal of the Korean Society of Radiology 2024;85(1):222-229
Synchronous renal malignancies are seldom encountered or diagnosed post-renal resection. A combination of renal cell carcinoma (RCC) and urothelial carcinoma (UC) is most commonly reported.Typically, the RCC subtype is clear-cell RCC; however, a combination of collecting duct carcinoma (CDC) and UC has rarely been reported in the existing literature. Here, we present two cases of synchronous renal malignancy, specifically a combination of CDC and UC, in the ipsilateral kidney.
9.Calcuified right ventricular mass: A case report.
Ki Jin PARK ; Seong Gue KIM ; Jung Kuk SEO ; Bang Heon LEE ; Won Sang JUNG ; Yeong Hak KIM ; Heng Ok JEE
The Korean Journal of Thoracic and Cardiovascular Surgery 1993;26(7):548-551
No abstract available.
10.A Large Malignant Peripheral Nerve Sheath Tumor in the Neurofibromatosis Patient: A Case Report.
Dong Il CHOI ; Dong Kuk SEO ; Woo Sung JO ; Chul Hoon CHUNG ; Seong Jin CHO
Journal of the Korean Society of Plastic and Reconstructive Surgeons 2006;33(6):761-763
PURPOSE: Malignant peripheral nerve sheath tumors most often arise from the anatomically discernible peripheral nerve or neurofibroma. METHODS: A 55-year-old man had a rapidly growing pedunculated large mass on the sacrolumbar junction for 2 years. He has congenital neurofibromatosis type I. He had multiple caf-au-lait spots and multiple neurofibromas on the entire body. The mass developed from a subcutaneous nodule on the sacrolumbar junction and grew rapidly. The preoperative punch biopsy revealed a malignant peripheral nerve tumor. The mass was completely excised with 1 cm free margin above the deep fascial plane. RESULTS: There was no evidence of recurrence of tumor for 19 months of follow-up examination. CONCLUSION: Malignant peripheral nerve sheath tumor is very rare and has unique feature. We report a successful case of malignant peripheral nerve sheath tumor with the review of the literatures.
Biopsy
;
Follow-Up Studies
;
Humans
;
Middle Aged
;
Neurilemmoma
;
Neurofibroma
;
Neurofibromatoses*
;
Neurofibromatosis 1
;
Peripheral Nerves*
;
Peripheral Nervous System Neoplasms
;
Recurrence