Oncocytic Adrenocortical Carcinoma: A Rare Case Report

IF 0.1 Q4 ONCOLOGY Uroonkoloji Bulteni-Bulletin of Urooncology Pub Date : 2018-06-12 DOI:10.4274/UOB.975
O. Üçer, Oğuzcan Erbatu, A. Tan, T. Müezzinoğlu
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Abstract

Oncocytic neoplasms can be seen in various organs, but they are usually detected in the thyroid, salivary glands, and kidneys. They contain oncocytic tumor cells that are recognized by their broad, eosinophilic and granular cytoplasm due to anomalous mitochondrial collection (1). Oncocytic neoplasms of the adrenal gland are uncommon and are generally benign and nonfunctioning. These tumors are more common in women and on the left adrenal gland. To date, 147 cases have been reported (2). Recent reports indicate that about 20% of the adrenocortical oncocytic neoplasms show malignant components and 10-20% produce hormones which may cause symptoms of Cushing’s syndrome or virilism (3).
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嗜瘤性肾上腺皮质癌1例报告
癌细胞肿瘤可见于各种器官,但通常在甲状腺、唾液腺和肾脏中发现。它们含有嗜酸细胞肿瘤细胞,由于线粒体异常收集,这些细胞被其宽阔的、嗜酸性的和颗粒状的细胞质所识别(1)。肾上腺的癌细胞肿瘤是罕见的,通常是良性和无功能的。这些肿瘤在女性和左肾上腺更常见。迄今为止,已报告147例病例(2)。最近的报告表明,约20%的肾上腺皮质嗜酸细胞肿瘤表现出恶性成分,10-20%的肿瘤产生激素,可能导致库欣综合征或男性化症状(3)。
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