Hopf Silke, Buchalla Rüdiger, Scheil Folkert, Heusermann Ulrich, Börm Wolfgang
Department of Neurosurgery, Diakonissenhospital Flensburg, Marienhölzungsweg 2, 24939, Flensburg, Germany.
Department of Pathology, Diakonissenhospital Flensburg, Flensburg, Germany.
J Neurooncol. 2009 Oct;95(1):141-145. doi: 10.1007/s11060-009-9906-4. Epub 2009 May 15.
Skull metastases can occur with nearly all types of tumor. They frequently are asymptomatic, causing local swelling, which is usually painless and rarely leads to neurological dysfunction. Carcinoma of the ampulla of Vater is an uncommon tumor accounting for approximately 0.2% of all gastrointestinal malignancies, with an estimated incidence of less than 6 cases per 1,000,000 population per year. We report about an extremely rare case of a 54-year-old female patient with a right frontal skull metastases of an ampulla of Vater adenocarcinoma 5 years after pylorus-preserving pancreaticoduodenectomy. Literature review revealed only one published case of cranial bone metastases of carcinoma of the ampulla of Vater. To the best of our knowledge this is the first case report of skull metastases of ampullary adenocarcinoma after a symptom-free interval of 5 years after R0 resection of the primary tumor, and the second published case that involves the skull.
几乎所有类型的肿瘤都可能发生颅骨转移。它们通常无症状,会引起局部肿胀,这种肿胀通常无痛,很少导致神经功能障碍。 Vater壶腹癌是一种罕见的肿瘤,约占所有胃肠道恶性肿瘤的0.2%,估计每年每100万人口中的发病率不到6例。我们报告了一例极为罕见的病例,一名54岁女性患者在保留幽门的胰十二指肠切除术后5年出现了Vater壶腹腺癌的右额颅骨转移。文献综述显示,仅有一例关于Vater壶腹癌颅骨转移的病例报道。据我们所知,这是首例原发性肿瘤R0切除术后5年无症状期后出现壶腹腺癌颅骨转移的病例报告,也是第二例涉及颅骨的已发表病例。