1.Congenital Immature Teratoma arising from the Tongue: Report of an autopsy case.
Jung Hoon YOON ; Kyi Beom LEE ; Chan Il PARK
Korean Journal of Pathology 1986;20(2):187-190
Congenital immature teratoma of the tongue is a exceedingly rare form of epignathus. We report here an autopsy case of a huge immature teratoma protruding from the tongue of a newborn female infant. The mass obstructed the mouth and caused hydramnios. The mother's serum level of alpha-fetoprotein was elevated, and the tumor was identified by a ultrasonogram subsequently done. Discussion on the histogenesis of epignathus was made through a review of literatures.
Infant
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Male
;
Female
;
Infant, Newborn
;
Humans
2.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
3.A Case of Congenital Megakaryoblastic Leukemia Accompanied by Down Syndrome Which was Diagnosed by Autopsy Findings.
Il Kyung KIM ; Dong Beom LEE ; Jung Sik MIN ; Chang Hee CHOI ; Je Geun CHI
Journal of the Korean Pediatric Society 1989;32(2):262-269
No abstract available.
Autopsy*
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Down Syndrome*
;
Leukemia*
;
Megakaryocyte Progenitor Cells*
4.A Case of Congenital Megakaryoblastic Leukemia Accompanied by Down Syndrome Which was Diagnosed by Autopsy Findings.
Il Kyung KIM ; Dong Beom LEE ; Jung Sik MIN ; Chang Hee CHOI ; Je Geun CHI
Journal of the Korean Pediatric Society 1989;32(2):262-269
No abstract available.
Autopsy*
;
Down Syndrome*
;
Leukemia*
;
Megakaryocyte Progenitor Cells*
5.Skin Staple Found at the Intractable Hypertrophic Scar Lesion.
Jin Woong JUNG ; Jun Beom LEE ; Jun Il KWON ; Young Wook RYOO ; Sung Ae KIM
Korean Journal of Dermatology 2017;55(7):466-467
No abstract available.
Cicatrix, Hypertrophic*
;
Skin*
6.Predictive Factors for Residual Neoplasia after Large Loop Excision of Transformation Zone(LLETZ) in the Treatment of Cervical Intraepithelial Neoplasia.
Yong Beom KIM ; Seong Il KIM ; Soon Sup SHIM ; Chul Min LEE ; Jae Weon KIM ; Noh Hyun PARK ; Yong Sang SONG ; Soon Beom KANG ; Hyo Pyo LEE
Korean Journal of Obstetrics and Gynecology 2000;43(3):481-487
OBJECTIVE: Large loop excision of transformation zone(LLETZ) is gaining popularity as an alternative to other ablative or cone methods for the treatment of cervical intraepithelial neoplasia(CIN). The optimal management of CIN after LLETZ, however, remains controversial and the reliable predictors of residual disease after LLETZ have not been consistently identified. This study was performed to identify factors to predict residual disease after LLETZ. METHODS: From August 1993 to July 1995, 133 patients who received subsequent hysterectomy after LLETZ in Department of Obstetrics and Gynecology at Seoul National University Hospital were retrospectively reviewed. Residual disease was defined as positive findings of CIN or further advanced findings in hysterectomy specimen. The age of patients, the severity of disease and the status of resection margin(RM) were analyzed for predictive values of residual disease. The Chi-square test, Fisher's exact test and Student t-test were used for statistical analysis. RESULTS: The residual disease after hysterectomy was negative in 85.7%(114/133) and positive in 14.3%(19/133). Among 19 cases with positive residual disease, 3 cases were revealed to be microinvasive cervical cancer. The mean age of patients with no residual disease was 42.5 years(range; 27-71) and that of patients with residual disease was 49.1 years(range; 33-72). Nine out of 94 cases(9.6%) with negative RM and 10 out of 39 cases(25.6%) with positive RM in LLETZ had residual disease. Two out of 14 cases(14.3%) with CIN II and 17 out of 119 cases(14.3%) with CIN III in LLETZ had residual disease. The success of LLETZ which means no residual disease was influenced by the age of patients(p=0.005) and the status of resection margin of LLETZ(p=0.032). CONCLUSION: The negative resection margin in LLETZ does not always guarantee that there is no residual disease. Close preoperative workup and more aggressive treatment plan(wide conization or hysterectomy) should be considered in patients who has higher possibility of positive residual disease such as old age and positive resection margin in LLETZ.
Cervical Intraepithelial Neoplasia*
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Conization
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Gynecology
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Humans
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Hysterectomy
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Obstetrics
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Retrospective Studies
;
Seoul
;
Uterine Cervical Neoplasms
7.A Critical Case of Wernicke's Encephalopathy Induced by Hyperemesis Gravidarum.
Byung Ju KANG ; Min Gu KIM ; Jwa Hoon KIM ; Mingee LEE ; Sang Beom JEON ; Ha Il KIM ; Jin Won HUH
Korean Journal of Critical Care Medicine 2015;30(2):128-131
Wernicke's encephalopathy is a reversible but potentially critical disease caused by thiamine deficiency. Most patients complain of symptoms such as ophthalmoplegia, ataxia and confusion. Heavy alcohol drinking is commonly associated with the disease, but other clinical conditions also can provoke it. In pregnant women, hyperemesis gravidarum can lead to the depletion of body thiamine due to poor oral intake and a high metabolic demand. We report a case of Wernicke's encephalopathy following hyperemesis gravidarum in a 36-year-old female at 20 weeks of pregnancy, who visited our hospital because of shock with vaginal bleeding. This case suggests that although the initial presentation may include atypical symptoms (e.g., shock or bleeding), Wernicke's encephalopathy should be considered, and thiamine replacement should be performed in pregnant women with neurologic symptoms and poor oral intake.
Acute Kidney Injury
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Adult
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Alcohol Drinking
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Ataxia
;
Female
;
Humans
;
Hyperemesis Gravidarum*
;
Neurologic Manifestations
;
Ophthalmoplegia
;
Pregnancy
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Pregnant Women
;
Shock
;
Thiamine
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Thiamine Deficiency
;
Uterine Hemorrhage
;
Wernicke Encephalopathy*
8.Health Effects of Air Particle Produced in a Waste Treatment Plant on Residents Living in an Official Residence of Air Base.
Jae Beom PARK ; Min Goo LEE ; Young Rok CHO ; Il Joong PARK ; Tae Hyung MIN
Korean Journal of Aerospace and Environmental Medicine 2001;11(2):107-113
BACKGROUND: This study was conducted to reveal the health effects of air pollution on the residents living near waste treatment plant. METHODS: We sampled 190 residents as the hogh exposed group, 192 residents as the moderate group, and 139 residents as the low exposed group according to the geographical distances from the waste treatment plant. Self-administered questionnaires for prevalence of respiratory disease, irritation symptoms of mucous membrane (eye, nose, thoat, skin, and respiratory tract), gastrointestinal symptoms, other nonspecific symptoms were conducted. We measured the concentrations of total suspened partcles, Zn, Cu, Cr, Ni, Pb, Cd and As in 3 exposed area. RESULT: Airborne concentrations of total suspended particles measured in exposed area were 485, 365, and 332 micro gram/m(3) which excees the limit value. Airborne concentrations of Zn, Cu, Cr, Ni, Pb, Cd and As were not excees the limit value. The prevalence of respiratory disease of high exposed group (16.8%) was significantly higher than that of moderate group (3.6%) and low exposed group (5.0%). The sysptom score of irrtation sysptoms of mucous membrane, gastrointestinal sysptoms, and other nonspecific sysptoms were increased with exposed level. In multiple linear regression, exposure level was related to all sysptom scores significantly. CONCLUSION: These results suggest that the air pollution of waste treatment plant would influence prevalence of respiratory disease, induce irritation of mucous membrane, gastrointestinal symptoms, and other nonspecific sysptoms.
Air Pollution
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Linear Models
;
Mucous Membrane
;
Nose
;
Plants*
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Prevalence
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Skin
;
Surveys and Questionnaires
9.A Case of Small Cell Carcinoma of the Ovary.
Jin Hak KIM ; Kwang Rae KIM ; Jong Il BAIK ; Yong Sang SONG ; Soon Beom KANG ; Hyo Pyo LEE
Korean Journal of Gynecologic Oncology and Colposcopy 1993;4(2):82-87
Small cell carcinoma of the ovary has been identified as a specific histopathologic entity. The first II cases were reported by Dickersin et a1, 1982, Since then only 80 cases were reported in literature. This rare and highly aggresive melignancy primarily affeets ehildren and young women(10-40) and grows rapidly, with hypercalcemia occuring frequently. Abscence of effective treatment results in early mortality. Recently we have experienced one case of primary sma11 cell carcinoma of the ovary, which is presented with a brief review of the literature.
Carcinoma, Small Cell*
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Female
;
Hypercalcemia
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Mortality
;
Ovary*
10.Translational Read-Through of a Nonsense Mutation Causing Bartter Syndrome.
Hee Yeon CHO ; Beom Hee LEE ; Hae Il CHEONG
Journal of Korean Medical Science 2013;28(6):821-826
Bartter syndrome (BS) is classified into 5 genotypes according to underlying mutant genes and BS III is caused by loss-of-function mutations in the CLCNKB gene encoding for basolateral ClC-Kb. BS III is the most common genotype in Korean patients with BS and W610X is the most common CLCNKB mutation in Korean BS III. In this study, we tested the hypothesis that the CLCNKB W610X mutation can be rescued in vitro using aminoglycoside antibiotics, which are known to induce translational read-through of a nonsense mutation. The CLCNKB cDNA was cloned into a eukaryotic expression vector and the W610X nonsense mutation was generated by site-directed mutagenesis. Cultured polarized MDCK cells were transfected with the vectors, and the read-through was induced using an aminoglycoside derivative, G418. Cellular expression of the target protein was monitored via immunohistochemistry. While cells transfected with the mutant CLCNKB failed to express ClC-Kb, G418 treatment of the cells induced the full-length protein expression, which was localized to the basolateral plasma membranes. It is demonstrated that the W610X mutation in CLCNKB can be a good candidate for trial of translational read-through induction as a therapeutic modality.
Animals
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Bartter Syndrome/genetics/*pathology
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Chloride Channels/analysis/genetics/*metabolism
;
Cloning, Molecular
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Codon, Nonsense
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Dogs
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Humans
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Immunohistochemistry
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Madin Darby Canine Kidney Cells
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Microscopy, Confocal
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Mutagenesis, Site-Directed
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Recombinant Fusion Proteins/analysis/biosynthesis/genetics
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Transfection