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相關文獻
- Paraganglioma: 14-Year Treatment Experience
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題名 | Paraganglioma: 14-Year Treatment Experience=副神經節瘤:十四年之治療經驗 |
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作 者 | 廖宣凱; 蔡家騏; 劉滄柏; | 書刊名 | 臺灣癌症醫學雜誌 |
卷期 | 26:2 2010.04[民99.04] |
頁次 | 頁65-71 |
分類號 | 416.29 |
關鍵詞 | 副神經節瘤; 後腹腔腫瘤; 副交感神經腫瘤; 嗜鉻細胞瘤; 兒茶酚胺激素; Paraganglioma; Retroperitoneal tumor; Parasympathetic tumor; Pheochromocytoma; Catecholamine; |
語文 | 英文(English) |
中文摘要 | 副神經節瘤,在胚胎學上主要是來自神經脊細胞,並有交感及副交感兩種來源。絕 大多數均為偶發性而沒有家族史。它的臨床表現可以是壓迫效應,意外的發現,或是和 過多兒茶酚胺的相關症狀有關。我們回顧了14 年當中在本院的13 個病例。絕大多數的 腫瘤位在頭頸部,但是仍有一部份的腫瘤在後腹腔。外科手術的的切除不論是對良性或 惡性的腫瘤仍是主要的治療方法。本篇文章指出該腫瘤在本院好發位置,症狀,治療, 併發症,以及結果。 |
英文摘要 | Paragangliomas, arising from neural crest cells, can be divided into sympathetic and parasympathetic origin. Most paragangliomas are sporadic, without family history. The patterns of presentation are usually associated with mass effect, incidental discovery, and symptoms from excess catecholamine production. We reviewed the past 14 years, during which there were 13 cases reported in our hospital. Most of the tumors were in the head and neck region, and there were also many cases in our series found in the retroperitoneal area. Surgical excision is still the mainstay treatment for both benign and malignant paragagliomas. This article describes their location, symptoms, treatment, complications, and outcomes at our hospital. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。