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1.
Gut and Liver ; : 254-264, 2014.
Artículo en Inglés | WPRIM | ID: wpr-163243

RESUMEN

BACKGROUND/AIMS: The aim of this study was to evaluate the influence of recent chemotherapy on the patterns of the maximum-standardized uptake value (M-SUV) and sensitivity of 18F-fluoro-deoxyglucose positron emission tomography/computed tomography (18F-FDG-PET/CT) in colorectal cancer. METHODS: We retrospectively analyzed the FDG-PET/CT of 509 patients who underwent surgery for colorectal cancer. Subgroup analysis was performed according to chemotherapy status; 401 patients were not treated with chemotherapy and 108 patients were treated with chemotherapy within 6 months prior to surgery. Pathologic analysis of the surgical specimen was used as the gold standard. RESULTS: The M-SUV was significantly lower in patients treated with chemotherapy than in those not treated with chemotherapy in pathologically confirmed same stages of disease. The difference in the sensitivity of the M-SUV according to chemotherapy status was greatest using a cutoff M-SUV value of 6.4 (p<0.001). The longest diameter of the primary tumor was the most important factor that correlated with M-SUV of the primary tumor irrespective of the chemotherapy effect (p<0.001). The M-SUV of the primary tumor was not an independent predictor of lymph node metastasis in colorectal cancer. CONCLUSIONS: The results indicate that the M-SUV of FDG-PET/CT should be interpreted in the context of concurrent chemotherapy.


Asunto(s)
Anciano , Femenino , Humanos , Masculino , Antineoplásicos/efectos adversos , Quimioradioterapia Adyuvante/efectos adversos , Quimioterapia Adyuvante/efectos adversos , Neoplasias Colorrectales/tratamiento farmacológico , Fluorodesoxiglucosa F18 , Invasividad Neoplásica , Metástasis de la Neoplasia , Tomografía de Emisión de Positrones/métodos , Radiofármacos , Estudios Retrospectivos
2.
Korean Journal of Medicine ; : 405-410, 2013.
Artículo en Coreano | WPRIM | ID: wpr-225747

RESUMEN

Pancreatic neuroendocrine tumors (PNET) are rare, with approximately 2.2 in 1,000,000 people affected annually. In the classification of neuroendocrine tumors, glucagonomas are a functional PNET and comprise 1.6% of PNET. Glucagonoma syndrome is a paraneoplastic syndrome that is characterized by necrolytic migratory erythema, weight loss, anemia, and diabetes mellitus. Metastatic disease at presentation is common, but is often limited to the liver and regional lymph nodes. Sunitinib malate improves the progression-free and overall survival of PNET. This report presents a 45-year-old Asian woman with prolonged neutropenia after sunitinib treatment of a glucagonoma with multiple hepatic metastases. The severity of the neutropenia after the sunitinib treatment fluctuated from grade 1 to 4 repeatedly, with a non-febrile pattern. Ultimately, the patient did not recover from the neutropenia, even after stopping the sunitinib.


Asunto(s)
Femenino , Humanos , Anemia , Pueblo Asiatico , Diabetes Mellitus , Glucagonoma , Indoles , Hígado , Ganglios Linfáticos , Eritema Necrolítico Migratorio , Metástasis de la Neoplasia , Tumores Neuroectodérmicos Primitivos , Tumores Neuroendocrinos , Neutropenia , Páncreas , Síndromes Paraneoplásicos , Pirroles , Pérdida de Peso
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