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[嗜铬细胞瘤的诊断与治疗。48例报告]

[Diagnosis and treatment of pheochromocytoma. Report of 48 cases].

作者信息

Xiao X R

机构信息

General Hospital of People's Liberation Army.

出版信息

Zhonghua Wai Ke Za Zhi. 1992 Mar;30(3):159-62, 189-90.

PMID:1473388
Abstract

A total of 48 patients with pheochromocytoma were treated during 1965-1989. The incidence of pheochromocytoma was about 2% in hypertensive patients at same period. In this series, 31 (64.6%) had adrenal pheochromocytoma and 17 (35.4%) extra-adrenal pheochromocytoma. More than 50% of the patients showed such symptoms as hypertension, headache, sweating and palpitation. Urinary catecholamine level was significantly elevated in 97.6% of the patients. In tumor localization, CT showed an accurate diagnostic rate of 95.5% and ultrasonography 85.7%. The fluctuation of blood pressure and the amount of fluid requirement during operation in phenoxybenzamine-treated patients were lower than those in non-phenoxybenzamine-treated patients, but there was no statistically significant difference between < 14 days of treatment group and > 14 days of treatment group in phenoxybenzamine-treated patients. 47 patients underwent complete excision of tumor, except 1 patient with a gigantic tumor from the organs of Zuckerkandl. One patient died after operation.

摘要

1965年至1989年期间,共治疗了48例嗜铬细胞瘤患者。同期高血压患者中嗜铬细胞瘤的发病率约为2%。在该系列中,31例(64.6%)为肾上腺嗜铬细胞瘤,17例(35.4%)为肾上腺外嗜铬细胞瘤。超过50%的患者出现高血压、头痛、出汗和心悸等症状。97.6%的患者尿儿茶酚胺水平显著升高。在肿瘤定位方面,CT的准确诊断率为95.5%,超声检查为85.7%。接受苯苄胺治疗的患者术中血压波动及液体需求量低于未接受苯苄胺治疗的患者,但苯苄胺治疗患者中治疗<14天组与治疗>14天组之间无统计学显著差异。47例患者肿瘤完全切除,1例来自主动脉旁体的巨大肿瘤患者除外。1例患者术后死亡。

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