1.MR Findings of Choroid Plexus Papilloma: Case Report.
Joo Hyeong OH ; Tae Hoon KIM ; Woo Suk CHOI
Journal of the Korean Radiological Society 1994;30(4):643-646
PURPOSE: Choroid Plexus papilloma is a rare intracranial neoplasm that is most commonly found in the trigone of the lateral ventricle in children or in the fourth ventricle in adult. Extraventricular extension of choroid plexus papilloma has been rarely reported within the cerebellopontine angle (CPA) cistern. Authors report two cases of choroid plexus papilloma in the posterior fossa seen on magnetic resonance imaging (MRI). MATERIALS AND METHODS: MRI findings of two cases of choroid plexus papilloma in posterior fossa were retrospectively reviewed. RESULTS: In the first case, the tumor was in the fourth ventricle and extended to the left CPA cistern via the foramen of Luschka. In the second case, the tumor presented as an expansile mass of the of fourth ventricle and right lateral recess. Multiple signal voids of low intensity due to prominent feeding vessels and calcifications within the tumors were noted. CONCLUSION: This report demonstrates MR findings of choroid plexus papilloma in the posterior fossa with the brief review of the literatures.
Adult
;
Brain Neoplasms
;
Cerebellopontine Angle
;
Child
;
Choroid Plexus*
;
Choroid*
;
Fourth Ventricle
;
Humans
;
Lateral Ventricles
;
Magnetic Resonance Imaging
;
Papilloma, Choroid Plexus*
;
Retrospective Studies
2.A Case of Acute Mixed Lineage Leukemia (ANLL with TII) with neutropenic Enterocolitis.
Hyeon Joo CHOI ; Young Suk KOH ; Young Mee HONG ; Seung Joo LEE ; Kee Suk HONG ; Keum Ja CHOI
Journal of the Korean Pediatric Society 1990;33(9):1281-1287
No abstract available.
Enterocolitis, Neutropenic*
;
Leukemia*
3.A Case of Ehlers - Danlos Syndrome.
Yoing Jin JOO ; Sung Moon CHOI ; Young Ja CHOI ; Ho Suk SUNG
Korean Journal of Dermatology 1990;28(5):620-626
No abstract available.
4.EFFECTS OF BONE ENGAGEMENT TYPE&IMPLANT LENGTH ON STRESS DISTRIBUTION: A THREE DIMENSIONAL FINITE ELEMENT ANALYSIS.
Jeong Hwa CHOI ; Jung Suk HAN ; Ki Youl SEO ; Joo Ho CHOI
The Journal of Korean Academy of Prosthodontics 1999;37(5):687-697
A finite element analysis has been utilized to analyze stress and strain fields and design a new configuration in orthopedics and implant dentistry. Load transfer and stress analysis at implant bone interface are important factors from treatment planning to long term success. Bone configuration and quality are different according to anatomy of expecting implantation site. The purpose of this study was to compare the stress distribution in maxilla and mandible according to implant length and bone engagement types. A three dimensional axi-symmetric implant model(Nobel Biocare, Gothenburg, Sweden) with surrounding cortical and cancellous bone were designed to analyzed the effects of bone engagement and implant length on stress distribution ANSYS 5.5 finite element program was utilized as an interpreting tool. Three cases of unicortical anchorage model with 7, 10, 13mm length and four cases of bicortical anchorage model with 5, 7, 10 and 13mm lenght were compared both maxillary and mandibular single implant situatiion. Within the limits of study, following conclusions were drawn. 1. There is difference in stress distribution according to cortical and cancellous bone thickness and shape. 2. Maximum stress was shown at the top of cortical bone area regardless of bone engagement types. 3. Bicortical engagement showed less stress accumulation when compared to unicortical case overall. 4. Longer the implant fixture length, less the stress on cortical bone area, however there is no difference in mandibular bicortical engagement case.
Dentistry
;
Finite Element Analysis*
;
Mandible
;
Maxilla
;
Orthopedics
5.A Case Report of Duodenal Diaphragm Misdiagnosed as a Bulimia.
Yong Joo LEE ; Eun Kyeong LEE ; Kyeong Bin RHO ; Yun Lyeon KIM ; Suk Ja CHOI ; Yong Joo KIM
Korean Journal of Gastrointestinal Endoscopy 1995;15(3):545-551
Duodenal diaphragm is a rare congenital anomaly among the congenital duodenal obstructions. Its symptom and sign usually appear since birth if obstruction is complete. The clinical manifestations of incompletely obstructive duodenal diaphragm are intermittent vomiting, abdominal pain and poor weight gain. Diagnosis may be delayed in this case. Authors experienced a case of incomplete duodenal diaphragm with a central hole. A 29 months old girl presented failure to thrive, intermittent episodes of bloating, abdominal discomfort and occasional vomiting. The patient vomited every 10-14 days, then the abdominal pain and distention were relieved. She overate for about 10 days until the next projectile vomiting. The vomitus frequently contained food ingested several days previously. Plain x-ray films of abdomen showed marked gastric distention. Upper gastrointestinal series revealed marked distention of the duodenum with windsock configuration and radiolucent line at the third portion of the duodenum. On gastroscopic examination, gastric bezoar impacting the pyloric canal and antrum was noted. At operation, we found mucosal membrane in the third portion of the duodenum and bezoar(Chinese cabbage) above the membrane. Side-to-side duodeno-jejunostomy was performed and bezoar was removed. She was discharged on the 13th postoperative day without any complication.
Abdomen
;
Abdominal Pain
;
Bezoars
;
Bulimia*
;
Child, Preschool
;
Diagnosis
;
Diaphragm*
;
Duodenal Obstruction
;
Duodenum
;
Failure to Thrive
;
Female
;
Humans
;
Membranes
;
Parturition
;
Vomiting
;
Weight Gain
;
X-Ray Film
6.A Case of Ichthyosiform Sarcoidosis.
Suk Joo CHOI ; Eul Hee HAN ; Kyung Sool KWON ; Tae Ahn CHUNG
Korean Journal of Dermatology 1994;32(1):172-176
Although acquired ichthyosis has been associated with a number of systemic illnesses, an association with sarcoidosis has rarely been reported. We report a patient with aquired ichthyosis of the lower and upper extrimities whose diagnosis of cutaneous sarcoidosis was confirmed by histologic examination. Systemic involvement in the patient revealed occular, pulmonary and nerve disease. A diagnosis of sarcoidosis must be considered when a patient presents with acquired ichthyosis.
Diagnosis
;
Humans
;
Ichthyosis
;
Sarcoidosis*
7.A Case of Primary Cutaneous Plasmacytoma , Observed for 10 years.
Kyung Sool KWON ; Eul Hee HAN ; Tae Ahn CHUNG ; Suk Joo CHOI ; Joon Ho LEE
Korean Journal of Dermatology 1994;32(1):144-148
A 28-year-old female devei,oped five rice-sized erythematous telaniectatic solid papules of her left side of cheek and numerous light brownish flat papules of her face two years before visiting our department of dermatology. Biopsy results of the erythematous papule vere dermal infiltration by well-differentiated, however, somewhat atypical and varying sized plasma cells involving epidermis, and the flat papule was that of verwca plana. Bone marrow aspirate was essentially normal. Primary cutaneous plasmacytoma is a rare disease. A significant proportion of patients with this ent on to develop systemic disease with a poor prognosis. Our patient was not treatead, bit only excised partially for biopsy. All skin lesions involuted two years later spontaneously and rema ns well until now six years later without recurring.
Adult
;
Biopsy
;
Bone Marrow
;
Cheek
;
Dermatology
;
Epidermis
;
Female
;
Humans
;
Plasma Cells
;
Plasmacytoma*
;
Prognosis
;
Rare Diseases
;
Skin
8.Detection of human papillomavirus DNA using the polymerase chain reaction in paraffin-embedded biopsy specimens of condylomata acuminata.
Suk Joo CHOI ; Doo Chan MOON ; Kyung Sool KWON ; Tae Ahn CHUNG
Korean Journal of Dermatology 1993;31(4):508-516
BACKGROUND: Condylomata acuminata is a sexually transmitted cisease which is caused by the human papillomavirus(HPV). The types of HPV causing condylomata acuminata are HPV 6,11,16,18. HPV 16 and 18 are related to anogenital carcinoma. OBJECTIVE: The goals of this study were to determine the types cif HPV in condylomata acuminata, and to investigate the relationship between condylomata acuminata and anogenital carcinoma. MEHTODS: Polymerase chain reaction and restriction fragment le igth polymorphisms were performed in the paraffin-embedded tissues of 17 cases of condylomata acciminata. RESULTS: HPV DNA was detected in all of 17 cases of condylomata accuminata tested. HPV 6 and 11 were found in 53% (9/17) and 41% (7/17) of the samples, respectiiely. HPV 16 and/or 18, which are related to anogenital carcinovia, were not detected, except in one case in which HPV 16 was found to be superimposed with HPV 6 and 11. CONCLUSION: These results suggest that most of condylomata acumirata are caused by HPV 16 and 11, and there is not so much risk of this disease transforming into the aiogenital carcinoma.
Biopsy*
;
Condylomata Acuminata*
;
DNA*
;
Human papillomavirus 16
;
Human papillomavirus 6
;
Humans*
;
Polymerase Chain Reaction*
9.Histopathologic consideration of hepatocellular carcinoma.
Hae Joo NAM ; Dong Suk KIM ; Won Hee CHOI ; Tae Sook LEE
Yeungnam University Journal of Medicine 1992;9(2):351-358
Hepatocellular carcinoma represents approximately 90% of the primary liver cancers. Recently, its incidence tends to be increased. Thirsty seven cases from 1986 to 1991 diagnosed as hepatocellular carcinoma by resection were analyzed to know their histopathologic feature and related clinical findings. The average age at the time of resection was 53.1 years, with frequent occurrence in third and fourth decades. Microscopically, the trabecular type was the most frequent growth pattern (35.1%) and classic hepatocyte-like cell type was the most frequent cell type (75.7%). The tumors are mainly moderately differentiated and frequently associated with liver cirrhosis. In comparison of cytological differentiation with liver cirrhosis, there was a tendency for well-differentiated tumors to arise in cirrhotic livers more often than poorly differentiated tumors, and the tendency was statistically significant. But differentiation and tumor size did not show significant correlation. Also statistically significant correlations were not observed between the level of alpha-fetoprotein and tumor size, and between the level of alpha-fetoprotein and differentiation.
alpha-Fetoproteins
;
Carcinoma, Hepatocellular*
;
Incidence
;
Liver
;
Liver Cirrhosis
;
Liver Neoplasms
;
Pathology
10.A case of Beckwith-Wiedemann Syndrome.
Nam Joo HWANG ; Soo Mi BACK ; Yang Suk CHOI ; Son Sang SOE ; Hye Kyoung YOON
Journal of the Korean Pediatric Society 1990;33(3):373-379
No abstract available.
Beckwith-Wiedemann Syndrome*