Noguchi M, Taniya T, Ueno K, Yagi M, Izumi R, Konishi K, Miyazaki I
Operation Center, Kanazawa University Hospital, Japan.
Jpn J Surg. 1990 Jul;20(4):448-52. doi: 10.1007/BF02470830.
We report herein a rare case of a 26 year old woman with pheochromocytoma complicated by paralytic ileus. She presented with remarkable abdominal distension and respiratory difficulty but was effectively treated by surgical removal of the tumor with preoperative and operative management using alpha and beta adrenergic blocking agents. An excessive and persistent catecholamine production from large tumors or massive metastases characterizes this rare complication, and a review of the English and Japanese literature is given following this report.
我们在此报告一例罕见病例，一名26岁女性患有嗜铬细胞瘤并伴有麻痹性肠梗阻。她表现出明显的腹胀和呼吸困难，但通过术前及术中使用α和β肾上腺素能阻滞剂进行管理，并手术切除肿瘤，得到了有效治疗。这种罕见并发症的特征是大肿瘤或大量转移灶产生过量且持续的儿茶酚胺，本报告之后会对英文和日文文献进行综述。
