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1.
Laboratory Animal Research ; : 92-97, 2017.
Article in English | WPRIM | ID: wpr-204557

ABSTRACT

The objective of this study was to determine the effect of ionizing radiation (IR) exposure of parents on carcinogenesis of the next generation focusing on the epigenetic perspective to clarify the relationship between radiation dose and carcinogenesis in F1 generation SD rats. F1 generations from pregnant rats (F0) who were exposed to gamma rays were divided into three groups according to the dose of radiation: 10 rad, 30 rad, and untreated. They were intraperitoneally injected with 50 mg/kg of diethylnitrosamine (DEN). Carcinogenesis was analyzed by examining expression levels of tumor suppressor genes (TSG) and other related genes by methylation-specific polymerase chain reaction (MSP). DNA methylation in liver tissues was evaluated to discern epigenetic regulation of transgenerational carcinogenesis vulnerability following IR exposure. Numerous studies have proved that transcriptional inactivation due to hypermethylation of TSG preceded carcinogenesis. Results of this study revealed hypermethylation of tumor suppressor gene SOCS1 in group treated with 30 rad. In addition, genes related to DNA damage response pathway (GSTP1, ATM, DGKA, PARP1, and SIRT6) were epigenetically inactivated in all DEN treated groups. In the case of proto-oncogene c-Myc, DNA hypermethylation was identified in the group with low dose of IR (10 rad). Results of this study indicated that each TSG had different radiation threshold level (dose-independent way) and DEN treatment could affect DNA methylation profile irrelevant of ionizing radiation dose.


Subject(s)
Animals , Humans , Rats , Carcinogenesis , Diethylnitrosamine , DNA , DNA Damage , DNA Methylation , Epigenomics , Family Characteristics , Gamma Rays , Genes, Tumor Suppressor , Liver , Parents , Polymerase Chain Reaction , Proto-Oncogenes , Radiation, Ionizing
2.
Keimyung Medical Journal ; : 34-38, 2016.
Article in Korean | WPRIM | ID: wpr-121470

ABSTRACT

A 53-year-old male was admitted to our hospital for evaluation of the second kidney transplant. A Iliopsoas Bursitis was detected on diagnostic abdominopelvic computed tomography. He had undergone a coronary angiography (CAG) due to chest pain 1 month prior to his visit. At that time, he had experienced pain on his right back and flank for some time. We found no other causes or predisposing factors associated with that problem. Thus, we report on a case of iliopsoas bursitis after CAG.


Subject(s)
Humans , Male , Middle Aged , Bursitis , Causality , Chest Pain , Coronary Angiography , Kidney , Kidney Transplantation
3.
Journal of Rheumatic Diseases ; : 382-386, 2015.
Article in English | WPRIM | ID: wpr-72806

ABSTRACT

Giant cell arteritis (GCA) is a systemic vasculitis which typically occurs in persons over 50 years old. GCA is closely related to polymyalgia rheumatica (PMR). A temporal artery biopsy is the gold standard test for the diagnosis of GCA. Recently, there is increasing evidence for the role of 18F-fluorodeoxyglucose positron emission tomography (18F-FDG-PET) in diagnosis of vasculitis. Here, we report on a case of a 67-year-old Korean male who was diagnosed with atypical GCA in subclinical stage concomitant with PMR by 18F-FDG-PET. After treatment, abnormal findings of 18F-FDG-PET were improved.


Subject(s)
Aged , Humans , Male , Biopsy , Diagnosis , Giant Cell Arteritis , Giant Cells , Polymyalgia Rheumatica , Positron-Emission Tomography , Systemic Vasculitis , Temporal Arteries , Vasculitis
4.
Korean Journal of Medicine ; : 746-751, 2015.
Article in Korean | WPRIM | ID: wpr-46988

ABSTRACT

Intravascular large B-cell lymphoma (IVLBCL) is a rare subtype of non-Hodgkin's lymphoma (NHL) and that progresses rapidly and is usually fatal. Because it usually presents with nonspecific symptoms, such as fever, the early diagnosis of IVLBCL is very difficult and it is often misdiagnosed as another disease. Systemic lupus erythematosus (SLE) is an autoimmune disease that affects various organs. The clinical manifestation of SLE ranges from rash and arthritis through anemia and thrombocytopenia to serositis, nephritis, seizures, and psychosis. Thus, it can be easily confused with many other disorders. We report a case of IVLBCL mimicking SLE in the initial diagnosis.


Subject(s)
Anemia , Arthritis , Autoimmune Diseases , B-Lymphocytes , Diagnosis , Early Diagnosis , Exanthema , Fever , Lupus Erythematosus, Systemic , Lymphoma , Lymphoma, B-Cell , Lymphoma, Non-Hodgkin , Nephritis , Psychotic Disorders , Seizures , Serositis , Thrombocytopenia
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