1.Hypertriglyceridemia Associated with Use of Sunitinib to Treat a Metastatic Pancreatic Neuroendocrine Tumor.
Sanghoon YOO ; Insook WOO ; Yun Hwa JUNG ; Gyohui KIM ; Youngyun CHO ; Chi Wha HAN
Korean Journal of Medicine 2015;88(1):101-105
Sunitinib is a multi-target tyrosine kinase inhibitor used to treat gastrointestinal stromal tumors, renal cell carcinoma, and pancreatic neuroendocrine tumors. The most common adverse reactions are known to be nausea, fatigue, diarrhea, stomatitis, esophagitis, hypertension, skin toxicity (hand-foot syndrome), hypothyroidism, and reduction in the cardiac output of the left ventricle. Herein, we report the case of a 57 year-old female who visited our hospital complaining of epigastric pain. She had been taking sunitinib at 25 mg/day to treat a metastatic pancreatic neuroendocrine tumor. Upon computed tomography performed on admission, we observed that fluid had collected around the pancreas. Laboratory analysis revealed hypertriglyceridemia (triglycerides 993 mg/dL). Tyrosine kinase inhibitors are known to have limited effects on lipid metabolism. In this case, we suggest that hyperglycemia seems to have had a limited effect on lipid levels. We are rather of the view that hyperglycemia, a history of distal pancreatectomy, and hypothyrodisim, indirectly caused the observed hypertriglyceridemia.
Carcinoma, Renal Cell
;
Cardiac Output
;
Diarrhea
;
Esophagitis
;
Fatigue
;
Female
;
Gastrointestinal Stromal Tumors
;
Heart Ventricles
;
Humans
;
Hyperglycemia
;
Hypertension
;
Hypertriglyceridemia*
;
Hypothyroidism
;
Lipid Metabolism
;
Nausea
;
Neuroendocrine Tumors*
;
Pancreas
;
Pancreatectomy
;
Protein-Tyrosine Kinases
;
Skin
;
Stomatitis
2.Differentiation and characteristics of undifferentiated mesenchymal stem cells originating from adult premolar periodontal ligaments.
Seong Sik KIM ; Dae Woo KWON ; Insook IM ; Yong Deok KIM ; Dae Seok HWANG ; L Shannon HOLLIDAY ; Richard E DONATELLI ; Woo Sung SON ; Eun Sook JUN
The Korean Journal of Orthodontics 2012;42(6):307-317
OBJECTIVE: The purpose of this study was to investigate the isolation and characterization of multipotent human periodontal ligament (PDL) stem cells and to assess their ability to differentiate into bone, cartilage, and adipose tissue. METHODS: PDL stem cells were isolated from 7 extracted human premolar teeth. Human PDL cells were expanded in culture, stained using anti-CD29, -CD34, -CD44, and -STRO-1 antibodies, and sorted by fluorescent activated cell sorting (FACS). Gingival fibroblasts (GFs) served as a positive control. PDL stem cells and GFs were cultured using standard conditions conducive for osteogenic, chondrogenic, or adipogenic differentiation. RESULTS: An average of 152.8 +/- 27.6 colony-forming units was present at day 7 in cultures of PDL stem cells. At day 4, PDL stem cells exhibited a significant increase in proliferation (p < 0.05), reaching nearly double the proliferation rate of GFs. About 5.6 +/- 4.5% of cells in human PDL tissues were strongly STRO-1-positive. In osteogenic cultures, calcium nodules were observed by day 21 in PDL stem cells, which showed more intense calcium staining than GF cultures. In adipogenic cultures, both cell populations showed positive Oil Red O staining by day 21. Additionally, in chondrogenic cultures, PDL stem cells expressed collagen type II by day 21. CONCLUSIONS: The PDL contains multipotent stem cells that have the potential to differentiate into osteoblasts, chondrocytes, and adipocytes. This adult PDL stem cell population can be utilized as potential sources of PDL in tissue engineering applications.
Adipocytes
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Adult
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Antibodies
;
Azo Compounds
;
Bicuspid
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Calcium
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Cartilage
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Chondrocytes
;
Collagen Type II
;
Durapatite
;
Fibroblasts
;
Humans
;
Mesenchymal Stromal Cells
;
Multipotent Stem Cells
;
Osteoblasts
;
Periodontal Ligament
;
Periodontics
;
Stem Cells
;
Tissue Engineering
;
Tooth
3.A case of Pneumocystis jiroveci pneumonia after bendamustine-based chemotherapy for refractory diffuse large B-cell lymphoma.
Jeonghoon HA ; Yunhwa JUNG ; Yunduk JUNG ; Sanbin LEE ; Yoonseo LEE ; Insook WOO
Blood Research 2016;51(1):61-63
No abstract available.
B-Lymphocytes*
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Drug Therapy*
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Lymphoma, B-Cell*
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Pneumocystis jirovecii*
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Pneumocystis*
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Pneumonia*