1.The Usefulness of Diffusion Weighted Imaging in the Differential Diagnosis of Various Intracranial Cystic Lesions.
Yon Kwon IHN ; Jeong Su JUN ; Seong Su HWANG ; Jun Hyun BAIK ; Young Ha PARK
Journal of the Korean Radiological Society 2004;50(6):415-421
PURPOSE: The purpose of this study was to evaluate the usefulness of diffusion-weighted imaging (DWI) for the differential diagnosis of various intracranial cystic lesions. MATERIALS AND METHODS: This study included 19 patients (13 males, 6 females) with a mean age of 42.5 years. The final histopathological diagnoses for 14 patients were pyogenic brain abscess (n=3), glioblastoma (n=3), ependymoma (n=1), anaplastic astrocytoma (n=1), pilocytic astrocytoma (n=1), hemangioblastoma (n=2), arachnoid cyst (n=1), epidermoid (n=1) and schwannoma (n=1). The other cases of metastasis (n=4) and arachnoid cyst (n=2) were diagnosed on the basis of clinical, laboratory and imaging data. DWI imaging studies were performed with a 1.5 T MR system. A single shot spin echo EPI pulse sequence was applied. B values were set at 0 and 1000 sec/mm2. The apparent diffusion coefficient (ADC) were calculated from the ADC map of 10 different cystic brain lesions. Conventional MR imaging included T2WI, T1WI, FLAIR and contrast enhanced T1WI. We analyzed the location, nature, signal intensity on DWI, and the enhancement pattern of the lesions. RESULTS: All of the 3 cases of brain abscess, 1 of 4 cases of metastasis and 1 case of epidermoid showed hyperintensity on DWI. The mean ADC value of brain abscess (2 cases) was less than 1.15 (0.13x10-3 mm2/s). The mean ADC values of the other cystic lesions (8 cases) were variable, ranging from 2.840.66 to 3.100.16 (10-3 mm2/sec). CONCLUSION: DWI and ADC values were useful in the differential diagnosis of various intracranial cystic lesions, but some metastatic tumors may mimic a brain abscess on DWI. Therefore, a clinical correlation is mandatory.
Arachnoid
;
Astrocytoma
;
Brain
;
Brain Abscess
;
Diagnosis
;
Diagnosis, Differential*
;
Diffusion*
;
Ependymoma
;
Glioblastoma
;
Hemangioblastoma
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Neoplasm Metastasis
;
Neurilemmoma
2.A Case of Acute Lymphoblastic Leukemia Preceded by Aleukemic Prodrome.
Byoung Su PARK ; Hwang Min KIM ; Baek Keun LIM ; Seok Won PARK ; Young UH ; Mee Yon CHO
Korean Journal of Pediatric Hematology-Oncology 2001;8(1):120-125
Acute lymphoblastic leukemia (ALL), in general, can be diagnosed by detecting blasts in peripheral blood or bone marrow. Some of the cases of ALL do not show typical leukemic features, and only manifest as refractory anemia, thrombocytopenia, myelofibrosis and lymphocytic infiltration into bone marrow. Several months after presentation, they may reveal typical leukemic features and are diagnosed as ALL. This kind of leukemia is called ALL with aleukemic prodrome. Although the incidence of ALL with aleukemic prodrome is 1.5~2.2% of childhood ALL cases, it is rarely reported in Korea. We experienced a 6 month-old female infant who presented with refactory anemia and thrombocytopenia, and two serial of bone marrow examination revealed only myelofibrosis. She subsequently developed ALL 3 months later. We report this case with a brief review of related literatures.
Anemia
;
Anemia, Refractory
;
Bone Marrow
;
Bone Marrow Examination
;
Female
;
Humans
;
Incidence
;
Infant
;
Korea
;
Leukemia
;
Precursor Cell Lymphoblastic Leukemia-Lymphoma*
;
Primary Myelofibrosis
;
Thrombocytopenia
3.Serial Magnetic Resonance Imaging to Determine the Progression of Neglected Recalcitrant Rotator Cuff Tears: A Retrospective Multicenter Study.
Yon Sik YOO ; Jin Young PARK ; Chang Hyuk CHOI ; Nam Su CHO ; Chul Hyun CHO ; Tae Gang LIM ; Sang Don SIM ; Tae Yon RHIE ; Ho Won LEE ; Jong Ho JUNG ; Yong Beom LEE
Clinics in Shoulder and Elbow 2017;20(3):133-137
BACKGROUND: To determine the natural progression of conservatively treated rotator cuff tears, we evaluated changes in radiologic and clinical parameters in patients whose recalcitrant tears were neglected after conservative treatment. METHODS: A total of 73 patients with recalcitrant rotator cuff tears in spite of conservative treatment were included in this study. We measured changes in tear size and in the extent of fatty infiltration of the rotator cuff by comparing the initial and final follow-up magnetic resonance imagings (MRIs). To determine factors influencing the change in tear size, we collected the medical history of patients taken at the time of initial admission. RESULTS: The average follow-up period was 20.1 months, and the average increase in tear size across this period was 6.2 mm. In terms of steroid injection, we found that the increases in tear size of the steroid injection group (p=0.049) and of the sub-group that had received more than three steroid injections (p=0.010) were significantly greater than that of the non-steroid injection group. CONCLUSIONS: We found that the increase in cuff tear size was on average 6.2 mm across the follow-up period, indicating that neglecting cuff tears may cause them to progress into more severe tears. We also observed that a history of steroid injection might be a possible risk factor for a worse prognosis of cuff tears. Therefore, we suggest that patients with rotator cuff tears and a history of steroid injection are recommended aggressive modes of treatment such as surgery.
Follow-Up Studies
;
Humans
;
Magnetic Resonance Imaging*
;
Prognosis
;
Retrospective Studies*
;
Risk Factors
;
Rotator Cuff*
;
Tears*
4.Decreases in Casz1 mRNA by an siRNA Complex Do not Alter Blood Pressure in Mice.
Su Min JI ; Young Bin SHIN ; So Yon PARK ; Hyeon Ju LEE ; Bermseok OH
Genomics & Informatics 2012;10(1):40-43
Recent genomewide association studies of large samples have identified genes that are associated with blood pressure. The Global Blood Pressure Genetics (Global BPgen) and Cohorts for Heart and Aging Research in Genome Epidemiology (CHARGE) consortiums identified 14 loci that govern blood pressure on a genomewide significance level, one of which is CASZ1 confirmed in both Europeans and Asians. CASZ1 is a zinc finger transcription factor that controls apoptosis and cell fate and suppresses neuroblastoma tumor growth by reprogramming gene expression, like a tumor suppressor. To validate the function of CASZ1 in blood pressure, we decreased Casz1 mRNA levels in mice by siRNA. Casz1 siRNA reduced mRNA levels by 59% in a mouse cell line. A polyethylenimine-mixed siRNA complex was injected into mouse tail veins, reducing Casz1 mRNA expression to 45% in the kidney. However, blood pressure in the treated mice was unaffected, despite a 55% reduction in Casz1 mRNA levels in the kidney on multiple siRNA injections daily. Even though Casz1 siRNA-treated mice did not experience any significant change in blood pressure, our study demonstrates the value of in vivo siRNA injection in analyzing the function of candidate genes identified by genomewide association studies.
Aging
;
Animals
;
Apoptosis
;
Asian Continental Ancestry Group
;
Blood Pressure
;
Cell Line
;
Cohort Studies
;
Gene Expression
;
Genome
;
Heart
;
Humans
;
Kidney
;
Mice
;
Neuroblastoma
;
RNA, Messenger
;
RNA, Small Interfering
;
Transcription Factors
;
Veins
;
Zinc Fingers
5.Induction of Donor-Specific Tolerance: Is This Achievable?.
Eun Jin CHO ; Ji In PARK ; Jung Nam AN ; Yon Su KIM
The Korean Journal of Internal Medicine 2012;27(1):114-114
No abstract available.
Animals
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Antigen-Presenting Cells/immunology
;
Graft Rejection/immunology/*prevention & control
;
Graft Survival
;
*Histocompatibility
;
Humans
;
Immunosuppression/*methods
;
Intercellular Adhesion Molecule-1/immunology
;
Isoantigens/*immunology
;
Organ Transplantation/*adverse effects
;
*Transplantation Tolerance
6.Utility of In-House PCR for HLA-B27 Typing: Comparison of Concordance Rate between PCR Kit and In-House PCR.
Sun Young CHO ; Kwang Gil LEE ; Su Yon PARK ; Hee Joo LEE
The Korean Journal of Laboratory Medicine 2008;28(3):239-243
BACKGROUND: Commercial kits of PCR method are widely used in HLA-B27 typing; however, their cost is relatively high. In this study, we evaluated the utility of an in-house PCR method by comparing it with that of a commercial kit. METHODS: HLA-B27 typing was done in 188 patients by using two PCR methods, Absolute(TM) HLAB27 PCR kit (Biosewoom, Korea) and an in-house PCR method. The primers used in the in-house method were prepared by Bioneer (Korea). Both PCR tests were done by Gene Amp PCR System 9600 (Perkin-Elmer Centus Corp., USA). RESULTS: The commercial kit and in-house PCR showed 100% concordance rate with each other in HLA-B27 typing. Of 188 patients tested 72 (38.3%) were positive and 116 (61.7%) were negative by the both tests. Of 62 patients with ankylosing spondylitis, 50 were positive (80.7%). CONCLUSIONS: The in-house PCR is a reliable and cost-effective method and can replace or supplement commercial kits for HLA-B27 typing.
Adult
;
Female
;
HLA-B27 Antigen/blood/*genetics
;
Histocompatibility Testing/*methods
;
Humans
;
Male
;
Polymerase Chain Reaction/*methods
;
Reagent Kits, Diagnostic
;
Sensitivity and Specificity
7.Acute Marchiafava-Bignami Disease: Diffusion-Weighted MRI in Cortical and Callosal Involvement.
Yon Kwon IHN ; Seong Su HWANG ; Young Ha PARK
Yonsei Medical Journal 2007;48(2):321-324
Marchiafava-Bignami disease (MBD) is a fatal disorder characterized by demyelination of the corpus callosum. MRI, suggestive of corpus callosum demyelination with associated white matter involvement in both cerebral hemispheres, indicates a diagnosis of MBD. In this case, MR diffusion-weighted findings taken at an acute stage of MBD revealed lesions not only in the corpus callosum but also in the cerebral cortex. Lower apparent diffusion coefficient values of the corpus callosum and cortical lesions were associated with poor clinical outcome.
Middle Aged
;
Male
;
Humans
;
Demyelinating Diseases/*pathology
;
Corpus Callosum/*pathology
;
Brain/*pathology
;
Alcoholism/complications
8.Testing the Biobehavioral Family Model in Understanding the Eating Problems of Adolescent Girls.
Ji Young PARK ; Su Yon BAEK ; Hee Soon KIM ; Jung Ha LIM ; Tae Hyung KIM
Child Health Nursing Research 2013;19(3):228-237
PURPOSE: This study was done to test a hypothesized model, the Biobehavioral Family Model (BBFM), on the relationship of family emotional climate, security of parent-child relationship, depression symptoms and eating problems in adolescent girls, to further understanding of eating problems in this population. METHODS: With a convenience sample of 647 girls, aged 15 to 18, a self-report survey was conducted which included the Korean form of the Eating Attitude Test (EAT-26) to assess eating problems. RESULTS: The estimated results of the structural equation modeling indicated a good fit of data to the hypothesized model proposing that family emotional climate and security of parent-child relationship were associated with the risk of eating problems by way of depression symptoms. That is, negative family emotional climate and insecure parent-child relationship increased the risk of eating problems indirectly by way of depression symptoms. CONCLUSION: The findings are consistent with the BBFM, which suggests a psychobiologic influence of specific family processes on children's stress-sensitive physical disease activity by way of depression symptoms. Therefore, the applicability of the BBFM for understanding adolescent girls' eating problems is supported. The psychobiologic pathways from depression to eating pathology should be addressed in future studies.
Adolescent
;
Aged
;
Climate
;
Depression
;
Eating
;
Feeding and Eating Disorders
;
Humans
;
Parent-Child Relations
9.Surgical Treatment of a Suprarenal Abdominal Aortic Pseudoaneurysm that Recurred 20 Years after Aorto-renal Bypass in a Patient with Takayasu Arteritis.
Yang Jin PARK ; Seung Kee MIN ; Jongwon HA ; Yon Su KIM ; Sang Joon KIM
Journal of the Korean Society for Vascular Surgery 2008;24(1):56-59
Takayasu arteritis (TA) is a chronic systemic inflammatory disease that most commonly affects the aorta and its major branches. TA-induced renal artery stenosis (TARAS) can result in malignant hypertension, severe renal dysfunction, cardiac decompression and premature death. Surgical management for TARAS has been proved to be effective and safe, especially in the medically or interventionally-intractable cases. We report here on a 39-year-old patient with recently deteriorating hypertension and renal function because of a recurred RAS, for which he underwent "y-shaped" aorto-birenal reconstruction surgery 20 years ago. CT angiography showed bilateral diffuse calcified stenosis in the previous renal graft and there was a partial rupture of a pseudoaneurysm in the suprarenal abdominal aorta segment between the celiac axis and the renal graft. We performed descending thoracic aorto-abdominal aortic bypass together with a graft-renal bypass and exclusion of the pseudoaneurysm. The renal function was normalized and the blood pressure became stable without any antihypertensive medication. He recovered and was discharged without any complications.
Adult
;
Aneurysm, False
;
Angiography
;
Aorta
;
Aorta, Abdominal
;
Axis, Cervical Vertebra
;
Blood Pressure
;
Constriction, Pathologic
;
Decompression
;
Humans
;
Hypertension
;
Hypertension, Malignant
;
Hypertension, Renovascular
;
Mortality, Premature
;
Renal Artery Obstruction
;
Rupture
;
Takayasu Arteritis
;
Transplants
10.A Case of Autosomal Recessive Pseudohypoaldosteronism Type 1 with a Novel Mutation in the SCNN1A Gene.
Su Yon KIM ; Joo Hoon LEE ; Hae Il CHEONG ; Young Seo PARK
Journal of the Korean Society of Pediatric Nephrology 2013;17(2):137-142
Pseudohypoaldosteronism (PHA) is a condition characterized by renal salt wasting, hyperkalemia, and metabolic acidosis due to renal tubular resistance to aldosterone. Systemic PHA1 is a more severe condition caused by defective transepithelial sodium transport due to mutations in the genes encoding the alpha (SCNN1A), beta (SCNN1B), or gamma (SCNN1G) subunits of the epithelial sodium channel at the collecting duct, and involves the sweat glands, salivary glands, colon, and lung. Although systemic PHA1 is a rare disease, we believe that genetic studies should be performed in patients with normal renal function but with high plasma renin and aldosterone levels, without a history of potassium-sparing diuretic use or obstructive uropathy. In the present report, we describe a case of autosomal recessive PHA1 that was genetically diagnosed in a newborn after severe hyperkalemia was noted.
Acidosis
;
Aldosterone
;
Colon
;
Epithelial Sodium Channels
;
Humans
;
Hyperkalemia
;
Hyponatremia
;
Infant, Newborn
;
Lung
;
Plasma
;
Pseudohypoaldosteronism*
;
Rare Diseases
;
Renin
;
Salivary Glands
;
Sodium
;
Sweat Glands