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首页> 外文期刊>Urology Annals >Composite pheochromocytoma-ganglioneuroma of the adrenal gland: A case report with immunohistochemical study
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Composite pheochromocytoma-ganglioneuroma of the adrenal gland: A case report with immunohistochemical study

机译:肾上腺复合型嗜铬细胞瘤-神经节神经瘤:1例免疫组化研究报告

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摘要

Composite tumors of the adrenal medulla consisting of pheochromocytoma and ganglioneuroma are rare tumors accounting for less than 3% of all sympathoadrenal tumors. These tumors display more than one line of differentiation in which normal and neoplastic chromaffin cells are capable of differentiating into ganglion cells under the influence of nerve growth factors. To the best of our knowledge, we report the second case with a composite tumor of the adrenal medulla in a normotensive patient from India.
机译:由嗜铬细胞瘤和神经节神经瘤组成的肾上腺髓质复合瘤是罕见的肿瘤,占所有交感肾上腺肿瘤的不到3%。这些肿瘤表现出一种以上的分化,其中正常和赘生性嗜铬细胞能够在神经生长因子的影响下分化为神经节细胞。据我们所知,我们报道了另一例来自印度的血压正常患者的肾上腺髓质复合瘤。

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