Düster P
Klinik für Herz-, Thorax- und Gefässchirurgie, Klinikum der Johannes Gutenberg Universität, Mainz.
Zentralbl Chir. 2002 Jan;127(1):59-61. doi: 10.1055/s-2002-20223.
The Pierre-Marie-Bamberger syndrome is a rare paraneoplastic syndrome caused by bronchial carcinoma. Typical signs are symmetric periostoses on the diaphyses of the long tubular bones, clubbed fingers and toes with eye-glass shape of the nails, neuro-vegetative disturbances and dysproteinemia. We report a 37-year-old patient with long-term nicotine abusus, who attracted attention by symptoms of a Pierre-Marie-Bamberger syndrome. Further diagnostics revealed a tumor in the apex of the left lung. After lobectomy of the upper lobe of the left lung the symptoms are completly disappeared.
皮埃尔-玛丽-班贝格综合征是一种由支气管癌引起的罕见副肿瘤综合征。典型症状包括长管状骨干骺端的对称性骨膜增生、杵状指（趾）伴指甲呈眼镜状、神经-植物神经功能紊乱和蛋白异常血症。我们报告一名37岁长期滥用尼古丁的患者，其因皮埃尔-玛丽-班贝格综合征的症状引起关注。进一步检查发现左肺尖部有肿瘤。左肺上叶切除术后症状完全消失。
