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A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Primary renal carcinoid tumor with multiple metastases
Ming-Chieh Chiang1, Yen-Chen Ou, Chi-Rei Yang
1Division of Urology, Department of Surgery, Taichung Veterans General Hospital, Taichung, Taiwan, R.O.C.
Journal of the Chinese Medical Association : JCMA
|August 24, 2010
Summary
Primary renal carcinoid tumors are rare. This case study details a patient with widespread metastases who experienced no severe cancer-related morbidity after cytoreductive surgery, improving quality of life.
Area of Science:
- Oncology
- Nephrology
- Surgical Oncology
Background:
- Primary renal carcinoid tumors are exceptionally rare kidney neoplasms.
- Fewer than 60 cases have been documented in medical literature.
Observation:
- A 46-year-old male presented with a primary renal carcinoid tumor.
- The patient exhibited extensive metastases to the liver, para-aortic lymph nodes, and bone at initial diagnosis.
Findings:
- Cytoreductive surgery was performed, prioritizing the patient's quality of life.
- The patient remained free from severe cancer-related morbidity for one year post-surgery.
Implications:
- This case highlights the potential for cytoreductive surgery in managing rare metastatic renal carcinoid tumors.
- Maintaining quality of life is a key consideration in treatment decisions for advanced-stage rare cancers.
- Further research into the long-term outcomes of such rare malignancies is warranted.
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