Singh Mansher, Ricci Joseph A, Talbot Simon G, Chiocca E Antonio, Dunn Ian F, Caterson Edward J
*Division of Plastic Surgery, Department of Surgery †Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
J Craniofac Surg. 2015 Nov;26(8):2289-92. doi: 10.1097/SCS.0000000000002218.
Metastatic tumors are the most common cranial neoplasms in adults. Skull metastases from rare primary tumors, such as cholangiocarcinoma or pancreatic neuroendocrine tumor, are extremely uncommon and rarely reported. Given the scarcity and variation of these rare skull metastases, treatments and outcomes of such patients are of interest to treating surgeons. The authors describe the treatment algorithm, course, and outcomes of 2 patients with rare gastrointestinal skull metastases. The first patient had intrahepatic cholangiocarcinoma metastatic to the skull, while the second patient developed a solitary skull metastasis secondary to a pancreatic neuroendocrine tumor. As part of this report, the authors include a literature review of rare skull metastases as well as the treatment of these 2 patients. Both the patients ultimately underwent successful resection of the tumor for relief of their clinical symptoms. Wide resections in both patients necessitated reconstruction using a free latissimus dorsi muscle flap in both the patients. Preoperative embolization of the hypervascular cholangiocarcinoma skull metastasis was performed prior to resection in the first patient. To date, there have been only 4 such reports of skull metastases from intrahepatic cholangiocarcinoma and limited reported cases of isolated skull metastases from a pancreatic neuroendocrine tumor.In patients with large or numerous skull metastasis from rare primary tumors, surgical resection should be considered for symptomatic improvement. In cases of hypervascular lesions, preoperative embolization can be considered to decrease the intraoperative bleeding. Free tissue transfers using myocutaneous flaps such as latissimus dorsi help in obliterating dead space, and creating a healthy soft tissue envelope to withstand postoperative radiation treatment. In addition, a chimeric flap can be designed to include additional muscle or soft tissue to obliterate and exclude the sinus cavities.
转移性肿瘤是成人中最常见的颅内肿瘤。来自罕见原发性肿瘤(如胆管癌或胰腺神经内分泌肿瘤)的颅骨转移极为罕见,报道也很少。鉴于这些罕见颅骨转移的稀缺性和多样性,此类患者的治疗方法和预后情况是外科治疗医生所关注的。作者描述了2例罕见胃肠道来源颅骨转移患者的治疗方案、病程及预后。首例患者为肝内胆管癌转移至颅骨,第二例患者继发于胰腺神经内分泌肿瘤的孤立性颅骨转移。作为本报告的一部分,作者对罕见颅骨转移以及这2例患者的治疗进行了文献综述。两名患者最终均成功切除肿瘤以缓解临床症状。两名患者均进行了广泛切除,均需要使用背阔肌游离肌皮瓣进行重建。首例患者在切除前对高血供的胆管癌颅骨转移灶进行了术前栓塞。迄今为止,仅有4例肝内胆管癌颅骨转移的报告,以及有限的胰腺神经内分泌肿瘤孤立性颅骨转移的报道病例。对于来自罕见原发性肿瘤的大型或多发颅骨转移患者,为改善症状可考虑手术切除。对于高血供病变,可考虑术前栓塞以减少术中出血。使用背阔肌等肌皮瓣进行游离组织移植有助于消除死腔,并形成健康的软组织包膜以耐受术后放疗。此外,可设计嵌合皮瓣以包括额外的肌肉或软组织来消除并封闭鼻窦腔。