[家族性嗜铬细胞瘤]
[Familial pheochromocytoma].
作者信息
Hartmann N, Terhorst B
出版信息
Urologe A. 1984 Jul;23(4):219-22.
PMID:6540918
Abstract
A familial pheochromocytoma disease is described on the basis of two siblings and a cousin. The main symptoms consisted of troubles with the eyes, inclination to perspire and high blood pressure. Special in this family disease was the marriage between relatives. The method of surgery consisted in a transverse upper abdominal incision with excellent surgical exposure.
摘要
基于两名兄弟姐妹和一名堂兄弟，描述了一种家族性嗜铬细胞瘤疾病。主要症状包括眼部问题、多汗倾向和高血压。这种家族性疾病的特殊之处在于亲属之间的婚姻。手术方法是采用上腹部横切口，手术视野极佳。
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