1.Primary Intracranial Choriocarcinoma: Case Report.
Jeong Pill PARK ; Houng Bong MOON ; Jae Hong JO ; Hyeun Won JO ; Hayk PARK ; Sung Moon YOON
Journal of Korean Neurosurgical Society 1993;22(12):1364-1368
Primary intracranial choriocarcinoma is a extremely rare neoplasm since the case was reported by Askanasy, in 1906, there have been 35 reported, even if germinal neoplasms containing chorocarcinoma-like tissue are added. But pure choriocarcinoma was rarely reported. The purpose of this paper is to report a case of 18-year-old boy with tumor in subependymal region around left frontal horn, which was present with high level of serum beta chain of chorionic gonadotropin(B-HCG) and was verified as germine choriocarcinoma by biopay.
Adolescent
;
Animals
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Choriocarcinoma*
;
Chorion
;
Female
;
Horns
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Humans
;
Male
;
Pregnancy
2.Purification and Characterization of Transforming growth factor - beta1 from Human Platelets.
Eun Jo KO ; Jong Won LEE ; Sang Uk NHAM ; Eui Yul CHOI ; Gie Taek CHUN ; Se Won YIE ; Pyeung Hyeun KIM
Korean Journal of Immunology 1998;20(1):1-8
Transforming growth factor-j31 (TGF-p1) has potential for therapeutic use in common clinical conditions for which there are no adequate pharmacological agents. However, in vivo studies using TGF-p1 were hindered by high price of this cytokine. As a first step towards large scale purification of TGF-p1, it was purified in a small scale (10 unit platelets) from human platelets by four purification steps: platelet extraction, gel filtration, cation exchange chromatography, and reversed phase high performance liquid chromatography (HPLC). A single protein band with a molecular weight of 25 Kd corresponding to purchased TGF-p1 (R8D Systems) was confirmed by silver staining after SDS-polyacrylamide gel electrophoresis (SDS-PAGE) of eluant from reversed phase HPLC. Recovery (%) of each step was about 50-60%, resulting in the final recovery of 20% based on the detection by a sandwich ELISA. Approximately, 3.7 p,g of purified TGF-p1 was obtained from 18 pg of platelet extracts. This result was confirmed by receptor (TGF-j31 type II) ELISA and bioassay using a mink lung epithelial'cell line (MV1LU). Further, in vitro characterization study showed that purified TGF-p1 inhibits G1/S transition of LPS-activated murine spleen B cells and increases surface IgA expression by the same cell population, which are typical activities of TGF-p1 in B cell differentiation. Taken together, the results from the present study reveals that purified TGF-p1 is fully biologically active and our purification methodology could be usbful to obtain a large scale of recombinant TGF-p1 in the future.
B-Lymphocytes
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Biological Assay
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Blood Platelets
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Cell Cycle
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Cell Differentiation
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Chromatography
;
Chromatography, Gel
;
Chromatography, High Pressure Liquid
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Chromatography, Liquid
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Electrophoresis
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Enzyme-Linked Immunosorbent Assay
;
Humans*
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Immunoglobulin A
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Lung
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Mink
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Molecular Weight
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Silver Staining
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Spleen
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Transforming Growth Factors*
3.Mortality, prognostic factor and cause of death of acute myocardial infarction in Korean patients: single center experience.
Ji Hoon KANG ; Jong Seon PARK ; Jang Won SON ; Hyeun Su JO ; Jun Ho BAE ; Geu Ru HONG ; Dong Gu SHIN ; Young Jo KIM ; Bong Seup SIM
Korean Journal of Medicine 2006;70(1):33-40
BACKGROUND: The number of patients suffering from acute myocardial infarction is on the increase in Korea due to the westernization of life style. Recent improvement of therapeutic stratigies have shown early mortality benefits in acute myocardial infarction. But we don't have data how many patients died and what's the cause of death in these patients. This study aimed to find out the mortality rate, cause of death and it's relevant prognostic factors of myocardial infarction (MI) patients who admitted alive, and to construct a database which will be used to develop a risk stratification strategy for the implementation of new preventive therapeutic modalities, such as implantable cardioverter-defibrillator (ICD). METHODS: Seven hundred and forty two MI patients admitted to our hospital from March, 1999 to August, 2002 were included in this study. The risk factors and survivals were evaluated by medical record searching and telephone survey in these patients. RESULTS: The average age was 64 years-old and 67% was male. During the mean follow up 20.7+/-15.4 months, total 105 cardiac death (14.2%) was occurred and cumulative mortality rate at 1 year and 2 year was 5.69% and 10.80%, respectively. Of the total 129 death, in-hospital death was 68 (cardiac death 48, non-cardiac death 20) and out of hospital death was 60 (cardiac death 57, non-cardiac death 4). When it comes to cause of death, most common cause of cardiac death was malignant arrhythmia. The proportion of malignant arrhythmia in cardiac death was 81.3% and 72% of in-hospital and out of hospital death, respectively. Multivariate analysis showed that old age, low LV ejection fraction and no percutaneous coronary intervention (PCI) treatment were independent risk factors for cardiac mortality. CONCLUSIONS: Myocardial infarction shows still high mortality rate despite the recent development of therapeutic strategy. As post-MI patients with low LVEF or no PCI shows high mortality, the early reperfusion therapy should be encouraged. Additionally, because malignant arrhythmia was one of the most in cause of cardiac death, ICD therapy to prevent sudden cardiac death should be considered in an active manner.
Arrhythmias, Cardiac
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Cause of Death*
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Death
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Death, Sudden, Cardiac
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Defibrillators, Implantable
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Follow-Up Studies
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Humans
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Korea
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Life Style
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Male
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Medical Records
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Middle Aged
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Mortality*
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Multivariate Analysis
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Myocardial Infarction*
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Percutaneous Coronary Intervention
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Reperfusion
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Risk Factors
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Telephone
4.A Case of Prenatally Diagnosed Klippel-Trenaunay-Weber Syndrome.
So Young KWON ; Yun Ah KIM ; Jong Won LEE ; Su Jin KIM ; Kyoung Jin LEE ; Ji Hyeun PARK ; Chang Jo CHUNG
Korean Journal of Perinatology 2003;14(4):416-421
Klippel-Trenaunay-Weber syndrome is a rare sporadically occurring congenital soft tissue anomaly characterized by cutaneous hemangiomata, hemihypertrophy and occasionally arteriovenous malformations(AVMs). No definite genetic defect has been identified. The appearance is a soft tissue mass of an extremity, usually affecting the adjacent trunk, hydrops fetalis, ascites, abdominal hemangiomatous masses, and hepatomegaly. When diagnosed prenatally, the disorder may be severe. Thrombocytopenia due to platelet consumption within the hemangioma and high output cardiac failure may complicate the outcome. Termination of pregnancy can be offered in severe forms, otherwise no alteration of management in expected. The management of newborns is primarily nonoperative, but some may benefit from surgical intervention. We report a case of Klippel-Trenaunay-Weber syndrome diagnosed prenatally by ultrasonogram in the second trimester and subsequently was terminated, with a brief review of literature.
Ascites
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Blood Platelets
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Extremities
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Female
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Heart Failure
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Hemangioma
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Hepatomegaly
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Humans
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Hydrops Fetalis
;
Infant, Newborn
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Klippel-Trenaunay-Weber Syndrome*
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Pregnancy
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Pregnancy Trimester, Second
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Prenatal Diagnosis
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Thrombocytopenia
;
Ultrasonography
5.Papillary Thyroid Carcinoma Manifesting as an Autonomously Functioning Thyroid Nodule.
Ji Hyun KIM ; Gyeong Jae NA ; Ki Won KIM ; Hee Ja KO ; Sung Wan JEON ; Yeo Joo KIM ; Sang Jin KIM ; Hyeun Duk JO ; Chang Jin KIM
Endocrinology and Metabolism 2012;27(1):59-62
Hyperfunctioning thyroid carcinoma is very rare. Hence, radionuclide imaging of thyroid hot nodules usually suggests a benign tumor, and less than 4% of cases have been reported as malignant. We would like to present a case of a hyperfunctioning papillary thyroid carcinoma that was initially treated with radioactive iodine. A 58-year-old woman was referred to our hospital for palpable thyroid nodule and a 5-kg weight loss within 6 months. Thyroid function test revealed thyrotoxicosis, and thyroid autoantibodies were absent. 99mTc thyroid scintigraphy showed a 2 x 2 cm-sized hyperactive hot nodule at the left lobe. Despite radioactive iodine treatment with a dose of 10 mCi 131I, thyroid function did not improve. Fine needle aspiration revealed papillary thyroid cancer. The patient underwent total thyroidectomy. Although clinical features and thyroid scans suggest a benign nodule, the possibility of malignancy should not be ruled out. Malignant thyroid hot nodules are rare; however, its possibility should be taken into account. Therefore, we suggest that ruling out malignancy by existing diagnostic guidelines can misdiagnose even a typical case with benign features. As thyroid nodule detection is getting sensitive and accurate, we present this case to discuss whether additional diagnostic approaches would be necessary for thyroid nodules.
Autoantibodies
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Biopsy, Fine-Needle
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Carcinoma
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Female
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Humans
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Iodine
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Middle Aged
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Thyroid Function Tests
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Thyroid Gland
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Thyroid Neoplasms
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Thyroid Nodule
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Thyroidectomy
;
Thyrotoxicosis
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Weight Loss
6.Taxonomic Study of Amanita Subgenus Lepidella and Three Unrecorded Amanita Species in Korea.
Chang Sun KIM ; Jong Won JO ; Young Nam KWAG ; Jae Hyeun KIM ; Bhushan SHRESTHA ; Gi Ho SUNG ; Sang Kuk HAN
Mycobiology 2013;41(4):183-190
Amanita Pers. is a well-known monophyletic mushroom genus with a broad distribution. However, the diversity of Korean Amanita species has been underestimated, and most taxonomic studies conducted in Korea have only investigated their morphological characteristics. This approach is frequently insufficient for correct identification in fungal classification; therefore, we constructed a phylogeny of Amanita subgen. Lepidella in order to understand the phylogenetic placements of 16 Amanita specimens collected in Korea in 2012. The phylogeny constructed using the sequence data of the internal transcribed spacers and the partial large subunit of ribosomal RNA identified nine Amanita species (A. citrina, A. excelsa var. spissa, A. flavipes, A. fritillaria, A. oberwinklerana, A. pallidorosea, A. rubescens, A. subjunquillea, and A. volvata); of these, A. fritillaria, A. oberwinklerana, and A. pallidorosea are new to Korea.
Agaricales
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Amanita*
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Classification
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Fritillaria
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Korea*
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Phylogeny
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RNA, Ribosomal
7.Lactoferrin Induces Tolerogenic Bone Marrow-Derived Dendritic Cells
Hui-Won PARK ; Sun-Hee PARK ; Hyeon-Ju JO ; Tae-Gyu KIM ; Jeong Hyun LEE ; Seung-Goo KANG ; Young-Saeng JANG ; Pyeung-Hyeun KIM
Immune Network 2020;20(5):e38-
Dendritic cells (DCs) are professional antigen-presenting cells (APCs) that initiate both T-cell responses and tolerance. Tolerogenic DCs (tDCs) are regulatory DCs that suppress immune responses through the induction of T-cell anergy and Tregs. Because lactoferrin (LF) was demonstrated to induce functional Tregs and has a protective effect against inflammatory bowel disease, we explored the tolerogenic effects of LF on mouse bone marrow-derived DCs (BMDCs). The expression of CD80/86 and MHC class II was diminished in LF-treated BMDCs (LF-BMDCs). LF facilitated BMDCs to suppress proliferation and elevate Foxp3 +induced Treg (iTreg) differentiation in ovalbumin-specific CD4 + T-cell culture. Foxp3 expression was further increased by blockade of the B7 molecule using CTLA4-Ig but was diminished by additional CD28 stimulation using anti-CD28 Ab. On the other hand, the levels of arginase-1 and indoleamine 2,3-dioxygenase-1 (known as key T-cell suppressive molecules) were increased in LF-BMDCs. Consistently, the suppressive activity of LF-BMDCs was partially restored by inhibitors of these molecules. Collectively, these results suggest that LF effectively causes DCs to be tolerogenic by both the suppression of T-cell proliferation and enhancement of iTreg differentiation. This tolerogenic effect of LF is due to the reduction of costimulatory molecules and enhancement of suppressive molecules.