首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Ectopic cortisol-producing adrenocortical adenoma in the renal hilum: histopathological features and steroidogenic enzyme profile
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Ectopic cortisol-producing adrenocortical adenoma in the renal hilum: histopathological features and steroidogenic enzyme profile

机译:肾门中异位产生皮质醇的肾上腺皮质腺瘤:组织病理学特征和类固醇生成酶谱

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Ectopic cortisol-producing adrenocortical adenomas (CPA) are extremely rare, and only four cases have previously been reported so far but the tumors were not ultrastructurally studied. Presented in this paper is the fifth case with ectopic CPA which was extensively examined to gain deeper insights in terms of the histopathological features and steroidogenic enzyme profile of the tumor. A 53-year-old woman complained of accidental discovery of left renal mass. She had a 5-year history of hypertension, weight gain, moon face, thin skin and systemic edema. These symptoms completely relieved after the tumor removal. Two years later, the above symptoms recurred, and a recurrent tumor was revealed in left renal hilum. The tumor was removed completely with relief of her symptoms of Cushing’s syndrome. Histologically and ultrastructurally, the tumor was composed of compact cells and clear cells, and the former was prominent, suggesting an active secretory function of the tumor. The adenoma tissue showed a strong immunostaining for Melan-A, 3beta-hydroxysteroid dehydrogenase (HSD3B2) and 17alpha-hydroxylase1 (CYP17A1). Expression pattern for 11beta-hydroxylase 1 (CYP11B1), 11beta-hydroxylase 2 (CYP11B2), CYP17 and HSD3B2 mRNA in ectopic CPA was similar to that in the adrenal CPA. In conclusion, in terms of histopathological characteristic and steroidogenic enzyme profile, ectopic CPA is similar to adrenal CPA, suggesting that they are of identical cell origin.
机译:异位产生皮质醇的肾上腺皮质腺瘤(CPA)极为罕见,迄今为止仅报道了4例病例,但尚未对肿瘤进行超微结构研究。本文介绍的是第五例异位CPA,经过广泛检查以从肿瘤的组织病理学特征和类固醇生成酶谱方面获得更深刻的见解。一名53岁的妇女抱怨意外发现左肾肿块。她有5年的高血压,体重增加,月亮脸,皮肤稀薄和全身水肿的病史。去除肿瘤后,这些症状完全缓解。两年后,上述症状再次出现,并且左肾门中发现了复发性肿瘤。肿瘤完全消除,缓解了库欣综合征的症状。从组织学和超微结构上看,该肿瘤由紧密细胞和透明细胞组成,前者突出,表明该肿瘤具有主动分泌功能。腺瘤组织对Melan-A,3β-羟类固醇脱氢酶(HSD3B2)和17α-羟化酶1(CYP17A1)表现出较强的免疫染色。异位CPA中11β-羟化酶1(CYP11B1),11β-羟化酶2(CYP11B2),CYP17和HSD3B2 mRNA的表达模式与肾上腺CPA中的表达模式相似。总之,就组织病理学特征和类固醇生成酶谱而言,异位CPA与肾上腺CPA相似,表明它们是相同的细胞起源。

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