Nigawara K, Suzuki T, Onodera T, Fukui K, Togashi S, Funyu T, Yamaya K, Terayama Y, Yamaguchi K
Department of Urology, Hirosaki University School of Medicine.
Nihon Naibunpi Gakkai Zasshi. 1987 Aug 20;63(8):923-33. doi: 10.1507/endocrine1927.63.8_923.
A case of malignant pheochromocytoma, with a recurrence 15 years after adrenalectomy and with an associated watery diarrhea, hypokalemia, achlorhydria syndrome, is reported. Histological evaluation of the tumors revealed composite malignant pheochromocytoma-ganglioneuroblastoma (well differentiated type). Vasoactive intestinal polypeptide and catecholamine levels were high both in the plasma and in the tumors. Somatostatin was also rich in the metastatic tumor of the liver, but not in the plasma. Immunohistochemical studies have demonstrated that immunoreactive vasoactive intestinal polypeptide is present in the ganglioneuroblastoma component, and that immunoreactive somatostatin is present in the pheochromocytoma component. Literature on the watery diarrhea, hypokalemia, achlorhydria syndrome associated with pheochromocytoma was reviewed.
报告了一例恶性嗜铬细胞瘤病例,该患者肾上腺切除术后15年复发,并伴有水样腹泻、低钾血症、无胃酸综合征。对肿瘤进行组织学评估显示为复合性恶性嗜铬细胞瘤-神经母细胞瘤(高分化型)。血浆和肿瘤中血管活性肠肽和儿茶酚胺水平均升高。生长抑素在肝脏转移瘤中含量丰富,但血浆中未检测到。免疫组织化学研究表明,免疫反应性血管活性肠肽存在于神经母细胞瘤成分中,免疫反应性生长抑素存在于嗜铬细胞瘤成分中。本文对与嗜铬细胞瘤相关的水样腹泻、低钾血症、无胃酸综合征的文献进行了综述。