肾透明细胞肉瘤引起的异位ACTH综合征。

Child nephrology and urology Pub Date : 1991-01-01
J C Hsiao, C P Yang, C J Lin, H Chuen
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引用次数: 0

摘要

这个7岁的女孩表现为库欣样样外观和肉眼血尿,被发现有右肾肿瘤。术前激素检测显示血浆ACTH水平极高,血浆皮质醇水平升高。行右侧根治性肾切除术,病理证实肿瘤为透明细胞肉瘤,是肾母细胞瘤的一种肉瘤变体。术后血浆ACTH水平显著下降,皮质醇水平也恢复正常。她接受了化疗和放疗,逐渐失去了库欣样外观。这是首例报道的肾透明细胞肉瘤伴异位ACTH综合征的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ectopic ACTH syndrome due to clear cell sarcoma of the kidney.

The 7-year-old girl presenting with cushingoid appearance and gross hematuria was found to have a right renal tumor. Preoperative hormonal assay revealed an extremely high plasma ACTH level and elevated plasma cortisol levels. Right radical nephrectomy was performed, and pathology proved the tumor to be a clear cell sarcoma, a sarcomatous variant of Wilms' tumor, of the kidney. Postoperative plasma ACTH level declined dramatically and cortisol levels returned to normal, too. She received chemotherapy and radiotherapy then and gradually lost her cushingoid appearance. This is the first reported case of clear cell sarcoma of the kidney with ectopic ACTH syndrome.

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