Lee John H, Barich Frank, Karnell Lucy Hynds, Robinson Robert A, Zhen Weining K, Gantz Bruce J, Hoffman Henry T
Department of Otolaryngology-Head and Neck Surgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa 52242, USA.
Cancer. 2002 Feb 1;94(3):730-7. doi: 10.1002/cncr.10252.
Malignant paragangliomas of the head and neck are rare, with previous reports limited to nine or fewer patients. The current review included 59 cases extracted from the National Cancer Data Base that were diagnosed between 1985-1996.
The primary criterion for inclusion in the current study was verified metastatic spread from a paraganglioma of the head and neck. Patterns of presentation and treatment as well as clinically relevant associations were demonstrated in contingency tables. Relative survival was used for analysis of outcome.
The average patient age at presentation was 44 years, and gender distribution was equivalent. Metastases were confined to regional lymph nodes in the majority of cases (68.6%), with carotid body tumors found to have an even higher rate of regional confinement (93.8%). Surgery was the most common treatment (76.3%). The use of adjuvant irradiation for regionally confined disease increased across time, from 27% (1985-1990) to 46% (1991-1996). The 5-year relative survival rate was 59.5% (76.8% for regionally confined carcinoma and 11.8% for distant metastasis). Among patients who were followed until death, those treated with adjuvant irradiation had a longer median survival (45 months) compared with those patients who were treated with surgery alone (12 months).
Malignant paraganglioma represents metastatic spread of a tumor type that, when restricted to the site of origin, is considered benign. Metastases from malignant paragangliomas of the head and neck usually are regionally confined. The primary management of a recognized malignancy should be directed toward complete surgical removal of the primary tumor and regional lymph nodes. Postoperative irradiation may be beneficial in slowing the progression of residual disease.
头颈部恶性副神经节瘤罕见,既往报道的患者数量不超过9例。本综述纳入了从国家癌症数据库中提取的59例在1985年至1996年间确诊的病例。
纳入本研究的主要标准是经证实的头颈部副神经节瘤转移扩散。在列联表中展示了临床表现和治疗模式以及临床相关关联。采用相对生存率分析预后。
患者就诊时的平均年龄为44岁,性别分布均衡。大多数病例(68.6%)的转移局限于区域淋巴结,发现颈动脉体瘤的区域局限率更高(93.8%)。手术是最常见的治疗方法(76.3%)。对于区域局限型疾病,辅助放疗的使用随时间增加,从27%(1985 - 1990年)增至46%(1991 - 1996年)。5年相对生存率为59.5%(区域局限型癌为76.8%,远处转移为11.8%)。在随访至死亡的患者中,接受辅助放疗的患者中位生存期较长(45个月),而单纯接受手术治疗的患者中位生存期为12个月。
恶性副神经节瘤代表一种肿瘤类型的转移扩散,该肿瘤类型局限于起源部位时被认为是良性的。头颈部恶性副神经节瘤的转移通常局限于区域。已确诊恶性肿瘤的主要治疗应针对完整手术切除原发肿瘤和区域淋巴结。术后放疗可能有助于减缓残留疾病的进展。