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1.
Korean Journal of Medicine ; : 132-137, 2010.
Article in English | WPRIM | ID: wpr-86562

ABSTRACT

Philadelphia chromosome-positive acute myeloid leukemia (Ph+AML) is a rare disease characterized by a poor prognosis with resistance to standard chemotherapy. We report a patient with Ph+AML with a minor BCR-ABL-positive mRNA transcript who achieved a hematologic, cytogenetic, and major molecular complete response after cytarabine-based chemotherapy followed by imatinib. After more than 6 months of continuous imatinib therapy, the patient is in continuous complete remission. Our results show that imatinib mesylate is effective in treating Ph+AML.


Subject(s)
Humans , Benzamides , Cytogenetics , Leukemia , Leukemia, Myeloid, Acute , Mesylates , Philadelphia , Philadelphia Chromosome , Piperazines , Prognosis , Pyrimidines , Rare Diseases , RNA, Messenger , Imatinib Mesylate
2.
Yeungnam University Journal of Medicine ; : 63-69, 2009.
Article in Korean | WPRIM | ID: wpr-73524

ABSTRACT

The incidence of coexisting hyperparathyroidism and empty sella syndrome is rare and the etiology and incidence of their coexistence is not known. The association of hyperparathyroidism and the empty sella syndrome may be related to multiple endocrine neoplasia (MEN) syndrome due to a genetic disorder. We experienced a rare case of hyperparathyroidism presenting as acute pancreatitis combined with empty sella. We report here a 37-year old female who manifested epigastric pain because of acute pancreatitis. She had hypercalcemia due to parathyroid adenoma. A pituitary gland was not visible in the sella turcica on MRI scans. On genetic analysis, she did not show a mutation of the MENIN gene. Empty sella is thought to be a coincidental finding with hyperparathyroidism.


Subject(s)
Female , Humans , Empty Sella Syndrome , Hypercalcemia , Hyperparathyroidism , Incidence , Magnetic Resonance Imaging , Multiple Endocrine Neoplasia , Pancreatitis , Parathyroid Neoplasms , Pituitary Gland , Sella Turcica
3.
Korean Journal of Medicine ; : 76-83, 2009.
Article in Korean | WPRIM | ID: wpr-163499

ABSTRACT

BACKGROUND/AIMS: Lung cancer is the leading cause of cancer-related death in Korea. Non-small cell lung cancer (NSCLC) comprises 80~85% of lung cancer. Positron emission tomography with [18F]fluorodeoxyglucose (FDG-PET) shows various levels of FDG uptake for patients with NSCLC. This study determined whether the standardized uptake value (SUV) of FDG uptake by PET is a prognostic factor for advanced NSCLC. METHODS: FDG-PET was performed in 59 patients with stage IIIb and IV NSCLC. The SUV was calculated for each patient. Overall survival (OS) and time to progression were calculated using the Kaplan-Meier method and evaluated with the log-rank test. The prognostic significance was assessed using univariate and multivariate analyses. RESULTS: A cutoff of 7 for the SUV gave the best criminative value. In the univariate analysis, performance status (p=0.02) and SUV (p=0.03) were significant predictors of OS. The patients with low SUVs (7, p=0.04). A multivariate Cox analysis identified performance status and the SUV as important for the prognosis. CONCLUSIONS:These results suggest that SUV is a significant prognostic factor in patients with advanced non-small cell lung cancer.


Subject(s)
Humans , Carcinoma, Non-Small-Cell Lung , Korea , Lung Neoplasms , Multivariate Analysis , Positron-Emission Tomography , Prognosis
4.
The Korean Journal of Internal Medicine ; : 287-291, 2007.
Article in English | WPRIM | ID: wpr-36334

ABSTRACT

Primary retroperitoneal mucinous cystadenocarcinoma is a rare tumor. Only about 30 such cases have been reported in the worldwide literature, and a few Korean cases have been reported. The pathogenesis is not clear, and coelomic metaplasia of the retroperitoneal mesothelium has gained wide support. There is no consensus on the appropriate treatment, but surgical exploration is needed for the diagnosis and treatment, and adjuvant chemotherapy may be recommended following complete surgical excision. The long-term prognosis has not been established. We report here on a 32-year-old woman who was diagnosed as having a retroperitoneal mucinous cystadenocarcinoma with mural nodules of sarcomatoid change. Tumor excision and adjuvant chemotherapy were done and the patient is doing well without any evidence of recurrence at 42 months postoperatively.


Subject(s)
Adult , Female , Humans , Cystadenocarcinoma, Mucinous/diagnosis , Retroperitoneal Neoplasms/diagnosis
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