Brown R J, Szymula N J, Loré J M
Arch Otolaryngol. 1978 Jul;104(7):395-8. doi: 10.1001/archotol.1978.00790070033009.
We reviewed 105 cases of neuroblastoma, which were seen at the Buffalo Children's Hospital between 1936 and 1976. We describe seven patients with primary neuroblastoma of the head and neck. The results of postmortem examination in two of these patients proved without any doubt that the tumor was primarily in the head and neck region. Although metastasis of neuroblastomas to the head and neck from more common primary sites in the abdomen, pelvis, or thorax is common, to our knowledge, well-documented primary head and neck lesions are quite rare. The prognosis of invasive neuroblastoma of the head and neck is poor, with rapid and widespread metastasis being the rule. However, some success has been reported with early and massive therapy that involves surgery, chemotherapy, and radiation therapy.
我们回顾了1936年至1976年间在布法罗儿童医院就诊的105例神经母细胞瘤病例。我们描述了7例原发性头颈部神经母细胞瘤患者。其中2例患者的尸检结果毫无疑问地证明肿瘤原发于头颈部区域。虽然神经母细胞瘤从腹部、骨盆或胸部等更常见的原发部位转移至头颈部很常见,但据我们所知,有充分记录的原发性头颈部病变相当罕见。头颈部侵袭性神经母细胞瘤的预后很差,通常会迅速广泛转移。然而,据报道,早期进行包括手术、化疗和放疗在内的大规模治疗取得了一些成功。