Niitsu Y, Goto Y, Maeda M, Tsushima N, Watanabe N, Kohgo Y, Urushizaki I
Department of Internal Medicine, Sapporo Medical College, Japan.
Aliment Pharmacol Ther. 1988 Jun;2(3):269-79. doi: 10.1111/j.1365-2036.1988.tb00697.x.
A case with WDHA syndrome due to VIPoma is reported. Injection of somatostatin analogue SMS 201-995 was followed by prompt suppression of vasoactive intestinal polypeptide levels (VIP), decreased stool volume, and restoration of the serum potassium concentration to normal. Long-term treatment with SMS 201-995 for up to 20 weeks produced excellent clinical control and a decrease in tumour size. No adverse effects were noted except for localized pain at the site of injection. This was overcome by using a continuous subcutaneous infusion pump which also enabled the effective daily dosage to be reduced and thereby adverse reactions to be avoided.
报告了1例因血管活性肠肽瘤(VIPoma)导致的WDHA综合征病例。注射生长抑素类似物SMS 201-995后,血管活性肠多肽(VIP)水平迅速受到抑制,粪便量减少,血清钾浓度恢复正常。使用SMS 201-995进行长达20周的长期治疗取得了良好的临床控制效果,肿瘤大小减小。除注射部位局部疼痛外,未观察到不良反应。使用连续皮下输注泵克服了这一问题,该泵还能降低有效日剂量,从而避免不良反应。