1.Direct Invasion of Thyroid Papillary Carcinoma to Esophagus Presenting as an Intraluminal Polypoid Mass Which Causes Hematemesis.
Min Young LEE ; Sang Eok KIM ; Hak Chan KIM ; Seung Hae HAN ; Dong Hoon SHIN ; Do Hyoung KIM ; In Gyun OH ; Byoung Youp KIM ; Woo Jin LEE ; June Sung LEE ; Hyun Wook BAIK ; Young Bin JEON
Korean Journal of Gastrointestinal Endoscopy 2001;23(6):466-469
We report an unusual case of metastatic thyroid papillary carcinoma directly invades the esophagus presenting as an intraluminal polypoid mass which causes hematemesis. The patient had a past medical history of thyroid nodule. Physical examination was unremarkable except the palpable thyroid mass. Esophagoscopy and esophagography revealed an intraluminal polypoid mass to the left of the cervical esophagus. Chest computed tomography showed round, homogenous, well-enhancing mass and calcifying thyroid nodule is found in front of the mass. Thyroid lobectomy and partial esophageal resection was performed. Microscopic finding showed typical features of thyroid papillary carcinoma. Metastatic thyroid papillary carcinoma should be included in the differential diagnosis of an intraluminal polypoid esophageal mass, particularly if the patient has a known thyroid tumor.
Carcinoma, Papillary*
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Diagnosis, Differential
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Esophagoscopy
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Esophagus*
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Hematemesis*
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Humans
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Physical Examination
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Thorax
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Thyroid Gland*
;
Thyroid Nodule
2.Small Animal PET Imaging with 124IFIAU for Herpes Simplex Virus Type 1 Thymidine Kinase Gene Expression in a Hepatoma Model.
Min Jeong CHAE ; Tae Sup LEE ; June Youp KIM ; Gwang Sun WOO ; Wee Sup JUMG ; Kwon Soo CHUN ; Jae Hong KIM ; Ji Sup LEE ; Jin Sook RYU ; Gi Jeong CHEON ; Chang Woon CHOI ; Sang Moo LIM
Nuclear Medicine and Molecular Imaging 2008;42(3):235-234
PURPOSE: The HSV1-tk gene has been extensively studied as a type of reporter gene. In hepatocellular carcinoma (HCC), only a small proportion of patients are eligible for surgical resection and there is limitation in palliative options. Therefore, there is a need for the develoopement of new treatment modalities and gene therapy is a leading candidate. In the present study, we investigated the usefulness of substrate, 2'-fluoro-2'-deoxy-1-beta-D-arabino-furanosyl-5-[124/125I]iodo- uracil ([124/125I]FIAU) as a non-invasive imaging agent for HSV1-tk gene therapy in hepatoma model using small animal PET. MATERIAL AND METHODS: With the Morris hepatoma MCA cell line and MCA-tk cell line which was transduced with the HSV1-tk gene, in vitro uptake and correlation study between [125I]FIAU uptake according to increasing numeric count of percentage of MCA-tk cell were performed. The biodistribution data and small animal PET images with [124I]FIAU were obtained with Balb/c-nude mice bearing both MCA and MCA-tk tumors. RESULTS: Specific accumulation of [125I]FIAU was observed in MCA-tk cells but uptake was low in MCA cells. Uptake in MCA-tk cells was 15 times higher than that of MCA cells at 480 min. [125I]FIAU uptake was linearly correlated (R2=0.964, p=0.01) with increasing percentage of MCA-tk numeric cell count. Biodistribution results showed that [125I]FIAU was mainly excreted via the renal system in the early phase. Ratios of MCA-tk tumor to blood acting were 10, 41, and 641 at 1 h, 4 h, and 24 h post-injection, respectively. The maximum ratio of MCA-tk to MCA tumor was 192.7 at 24 h. Ratios of MCA-tk tumor to liver were 13.8, 66.8, and 588.3 at 1 h, 4 h, and 24 h, respectively. On small aninal PET, [124I]FIAU accumulated in substantial higher levels in MCA-tk tumor and liver than MCA tumor. CONCLUSION: FIAU shows selective accumulation to HSV1-tk expressing hepatoma cell tumors with minimal uptake in normal liver. Therefore, radiolabelled FIAU is expected to be a useful substrate for non-invasive imaging of HSV1-tk gene therapy and therapeutic response monitoring of HCC.
Animals
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Arabinofuranosyluracil
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Carcinoma, Hepatocellular
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Cell Count
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Cell Line
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Genes, Reporter
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Genetic Therapy
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Herpes Simplex
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Herpesvirus 1, Human
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Humans
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Liver
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Liver Neoplasms, Experimental
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Methylmethacrylates
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Mice
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Polystyrenes
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Simplexvirus
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Statistics as Topic
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Uracil
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Ursidae
3.Imaging of Lung Metastasis Tumor Mouse Model using 18FFDG Small Animal PET and CT.
June Youp KIM ; Sang Keun WOO ; Tae Sup LEE ; Kyeong Min KIM ; Joo Hyun KANG ; Kwang Sun WOO ; Wee Sup CHUNG ; Jae Ho JUNG ; Gi Jeong CHEON ; Chang Woon CHOI ; Sang Moo LIM
Nuclear Medicine and Molecular Imaging 2007;41(1):42-48
PURPOSE: The purpose of this study is to image metastaic lung melanoma model with optimal pre-conditions for animal handling by using [18F]FDG small animal PET and clinical CT. MATERIALS AND METHODS: The pre-conditions for lung region tumor imaging were 16-22 h fasting and warming temperature at 30 degrees C. Small animal PET image was obtained at 60 min postinjection of 7.4 MBq [18F]FDG and compared pattern of [18F]FDG uptake and glucose standard uptake value (SUVG) of lung region between Ketamine/Xylazine (Ke/Xy) and Isoflurane (Iso) anesthetized group in normal mice. Metastasis tumor mouse model to lung was established by intravenous injection of B16-F10 cells in C57BL/6 mice. In lung metastasis tumor model, [18F]FDG image was obtained and fused with anatomical clinical CT image. RESULTS: Average blood glucose concentration in normal mice were 128.0+/-23.87 and 86.0+/-21.65 mg/dL in Ke/Xy group and Iso group, respectively. Ke/Xy group showed 1.5 fold higher blood glucose concentration than Iso group. Lung to Background ratio (L/B) in SUVG image was 8.6+/-0.48 and 12.1+/-0.63 in Ke/Xy group and Iso group, respectively. In tumor detection in lung region, [18F]FDG image of Iso group was better than that of Ke/Xy group, because of high L/B ratio. Metastatic tumor location in [18F]FDG small animal PET image was confirmed by fusion image using clinical CT. CONCLUSION: Tumor imaging in small animal lung region with [18F]FDG small animal PET should be considered pre-conditions which fasting, warming and an anesthesia during [18F]FDG uptake. Fused imaging with small animal PET and CT image could be useful for the detection of metastatic tumor in lung region.
Anesthesia
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Animals
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Animals*
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Blood Glucose
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Fasting
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Glucose
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Injections, Intravenous
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Isoflurane
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Lung*
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Melanoma
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Mice*
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Neoplasm Metastasis*