2.Cleidocranial dysostosis: a case report.
Sang Ho HA ; Sang Hong LEE ; Young Bae PYO ; Geun Sig RIM
The Journal of the Korean Orthopaedic Association 1992;27(4):1203-1207
No abstract available.
Cleidocranial Dysplasia*
3.A Case of Protein Energy Malnutrition After Whipples' s Operation.
Min Ah PARK ; Sang Geun HA ; Young Ho WON ; Inn Ki CHUN
Korean Journal of Dermatology 1994;32(1):130-133
Protein energy malnutrition occurs when inadequate protein and calories are ingested. PEM is not confined to children and is common in hospitalized patients. PEM is diagnosed by a weight loss and hypoalbuminemia. We report a case of PEM in a 27-year-old man after Whipple's operation. He had brittle hair, loss on the scalp and brownish colored papules with desquamation on extremities. Also he had erosion and fissuring on the perioral area and beef tongue. Treatment with zinc sulfate, albumin and vitamin resulted in a good response.
Adult
;
Child
;
Extremities
;
Hair
;
Humans
;
Hypoalbuminemia
;
Protein-Energy Malnutrition*
;
Scalp
;
Tongue
;
Vitamins
;
Weight Loss
;
Zinc Sulfate
4.A case of asphylaxiating thoracic dystrophy type II.
Sang Mi HA ; Soon Il LEE ; Moon Chul KIM ; Je Geun CHI
Journal of the Korean Pediatric Society 1992;35(12):1756-1761
No abstract available.
5.Two cases of Fournier's gangrene.
Eui Hun JEONG ; Geun Ha LIM ; Sang Joung LEE ; Young Taik HAN
Korean Journal of Urology 1991;32(3):505-508
In 1883 Fournier, a French venereologist, described 5 patients with unexplained fulminating gangrene of the male genitalia. Fournier emphasized 3 characteristics 1) the abrupt onset in a young, healthy male subjects, 2) the rapid progression to gangrene and 3) the absence of a discernible cause. As currently used by many authors, Fournier's gangrene describes a widely destructive, gangrenous process of the genitalia, with little regard for Fournier's original tenets of patient's age or definable etiology. Early identification and prompt initiation of medical and surgical therapy is imperative. We report two cases of Fournier's gangrene with brief review of the literatures.
Fournier Gangrene*
;
Gangrene
;
Genitalia
;
Genitalia, Male
;
Humans
;
Male
6.MR Imaging of Gestational Trophoblastic Tumors.
Hak Hee KIM ; Jae Hee LEE ; Ha Hun SONG ; Eun Ja LEE ; Taek Geun KIM ; Jin Bum PARK ; Hyun Kwon HA ; Sang Chun RO ; Mi Kyung JEE ; Jae Geun CHUNG
Journal of the Korean Radiological Society 1994;31(3):529-534
PURPOSE: To evaluate the MR findings of gestational trophoblastic tumor(GTT) in correlation with pathological results. MATERIALS AND METHODS: Nine patients who confirmed the diagnosis (four choriocarcinomas and five invasive moles) constituted the basis of our study. Pathologic specimens were taken from the tumors corresponding to the regions of interest on MR images. The MR images were analyzed in respect of the morphology and signal intensity of the tumors, uterine and adnexal vascularity, and the adnexal lesion. RESULTS: The MR findings of four choriocarcinomas were well-defined, hemorrhagic masses with central necrosis;the masses were hyperintense on Tl-weighted images. In contrast, the five invasive moles showed irregular and permeative masses with densely enhanced solid components and tiny cystic lesions. The trophoblastic proliferation, coagulation necrosis, and molar villi had variable signal intensities on Tl-and T2-weighted images. CONCLUSION: Our results suggest that MR imaging is a promising tool for noninvasive morphologic analysis of GTTS.
Choriocarcinoma
;
Diagnosis
;
Female
;
Humans
;
Hydatidiform Mole, Invasive
;
Magnetic Resonance Imaging*
;
Molar
;
Necrosis
;
Pregnancy
;
Trophoblastic Neoplasms*
;
Trophoblasts*
7.Four Cases of Gastric Hamartomatous Polyps without Polyposis Coli.
Jung Myung CHUNG ; Sang Hyuk LEE ; Youn Jae LEE ; Joon Yong JEONG ; Sang Young SEOL ; Hye Kyoung YOON ; Hee Geun HA ; Hee Seung WHANG
Korean Journal of Gastrointestinal Endoscopy 1996;16(6):994-999
Hamartoma is a very rare congenital tumor. A few cases of hamartomatous pol yps in the stomach were reported. Most of harrurtomatous polyps in the stomach occur in patients of polyposis coli. We have experienced four cases of gastric hamartomatous polyps without polyposis coli. There are some differences between previously reported cases and ours. In our casee, the distribution of age is from fourth to ninth decade, men and women ratio is 1: 1. The number of polyps are one in three cases and two in one case. The size of polyps is from 5mm to 12 mm. The location of polyps are various, but most common in antrum. We have experienced four cases which were different from previously reported ones and report them with a brief review of literatures.
Adenomatous Polyposis Coli*
;
Female
;
Hamartoma
;
Humans
;
Male
;
Polyps*
;
Stomach
8.Four Cases of Gastric Hamartomatous Polyps without Polyposis Coli.
Jung Myung CHUNG ; Sang Hyuk LEE ; Youn Jae LEE ; Joon Yong JEONG ; Sang Young SEOL ; Hye Kyoung YOON ; Hee Geun HA ; Hee Seung WHANG
Korean Journal of Gastrointestinal Endoscopy 1996;16(6):994-999
Hamartoma is a very rare congenital tumor. A few cases of hamartomatous pol yps in the stomach were reported. Most of harrurtomatous polyps in the stomach occur in patients of polyposis coli. We have experienced four cases of gastric hamartomatous polyps without polyposis coli. There are some differences between previously reported cases and ours. In our casee, the distribution of age is from fourth to ninth decade, men and women ratio is 1: 1. The number of polyps are one in three cases and two in one case. The size of polyps is from 5mm to 12 mm. The location of polyps are various, but most common in antrum. We have experienced four cases which were different from previously reported ones and report them with a brief review of literatures.
Adenomatous Polyposis Coli*
;
Female
;
Hamartoma
;
Humans
;
Male
;
Polyps*
;
Stomach
9.A case of fibroepithelial polyp of the ureter.
Sang Jong LEE ; Geun Ha LIM ; Eui Hun JOUNG ; Sang Tai KO ; Ki Yong SHIN ; Young Taik HAN
Korean Journal of Urology 1991;32(4):685-687
Fibroepithelial polyp of the ureter is a extremely rare benign tumor which is mesodermal origin. It should be suspected preoperatively in cases with a long history of loin pain or hematuria, or both, in a younger patient with the radiologic finding of long ureteric filling defect. Unfortunately. in the majority of cases reviewed. the diagnosis was not made preoperatively but the diagnostic confirmation was made intraoperatively or postoperatively. Herein, we report a case of fibroepithelial polyp or the ureter which was diagnosed preoperatively with ureteroscope. The management was local segmental excision and end-to-end anastomosis of the ureter.
Diagnosis
;
Hematuria
;
Humans
;
Mesoderm
;
Polyps*
;
Ureter*
;
Ureteroscopes
;
Ureteroscopy
10.A case of fibroepithelial polyp of the ureter.
Sang Jong LEE ; Geun Ha LIM ; Eui Hun JOUNG ; Sang Tai KO ; Ki Yong SHIN ; Young Taik HAN
Korean Journal of Urology 1991;32(4):685-687
Fibroepithelial polyp of the ureter is a extremely rare benign tumor which is mesodermal origin. It should be suspected preoperatively in cases with a long history of loin pain or hematuria, or both, in a younger patient with the radiologic finding of long ureteric filling defect. Unfortunately. in the majority of cases reviewed. the diagnosis was not made preoperatively but the diagnostic confirmation was made intraoperatively or postoperatively. Herein, we report a case of fibroepithelial polyp or the ureter which was diagnosed preoperatively with ureteroscope. The management was local segmental excision and end-to-end anastomosis of the ureter.
Diagnosis
;
Hematuria
;
Humans
;
Mesoderm
;
Polyps*
;
Ureter*
;
Ureteroscopes
;
Ureteroscopy