Kragel P J, Johnston C A
Arch Pathol Lab Med. 1985 May;109(5):470-2.
Composite adrenal tumors composed of both pheochromocytoma and ganglioneuroma are rare. To our knowledge, only two cases have been reported previously, displaying symptoms referable, in the first case to vasoactive intestinal polypeptide production and, in the second case, to catecholamine production. We report a case of composite pheochromocytoma-ganglioneuroma associated with renal angiomyolipoma and elevated urinary and serum catecholamine levels. Light and electron microscopic findings are described.
由嗜铬细胞瘤和神经节神经瘤组成的复合性肾上腺肿瘤很罕见。据我们所知,此前仅报道过两例,第一例表现出与血管活性肠肽分泌相关的症状,第二例则与儿茶酚胺分泌有关。我们报告一例复合性嗜铬细胞瘤 - 神经节神经瘤,伴有肾血管平滑肌脂肪瘤,且尿和血清儿茶酚胺水平升高。本文描述了其光镜和电镜检查结果。