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- W2360512012 abstract "Objective To study the clinic features of renal neurofibroma and to promote a better understanding of the disease. Methods The data of two cases of renal neurofibroma in brothers were analyzed and summarized. Palpable mass were the common symptoms of renal neurofibroma. Imaging features were not typical compared with other renal carcinomas. Immunohistochemical test was essential for the diagnosis of renal neurofibroma. Both cases underwent surgical excision. Results One case was followed up for 6 years and the other for 2 years,with no recurrence occurred. Conclusion Renal neurofibroma is a rare and benign tumor,probably related to heritage factors. Diagnosis depends on pathological and immunohistochemical methods. So far nephron sparing nephrectomy surgery has been the optimal treatment with good prognosis." @default.
- W2360512012 created "2016-06-24" @default.
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- W2360512012 date "2009-01-01" @default.
- W2360512012 modified "2023-09-27" @default.
- W2360512012 title "Two cases of renal neurofibroma in two brothers and literature review" @default.
- W2360512012 hasPublicationYear "2009" @default.
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