[冯·希佩尔-林道病中的嗜铬细胞瘤。3例]
[Pheochromocytoma in Von Hippel Lindau disease. 3 cases].
作者信息
Tourniaire J, Pradat P, Chalendar D
机构信息
Clinique Endocrinologique, Hôpital de l'Antiquaille, Lyon.
出版信息
Ann Endocrinol (Paris). 1995;56(6):609-12.
PMID:8787353
Abstract
Presenting 3 personally examined cases, the authors underline the incidence and the characteristics of pheochromocytoma associated with Von Hippel Lindau disease. In conclusion, a systematic screening for Von Hippel Lindau disease-often unrecognized to day-must be done in every patient presenting with pheochromocytoma.
摘要
作者通过展示3例亲自检查的病例，强调了与冯·希佩尔-林道病相关的嗜铬细胞瘤的发病率和特征。总之，对于每一位患有嗜铬细胞瘤的患者，都必须进行系统的冯·希佩尔-林道病筛查，而这种疾病目前常常未被识别。
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