Kahn L B
Cancer. 1976 Dec;38(6):2367-77. doi: 10.1002/1097-0142(197612)38:6<2367::aid-cncr2820380625>3.0.co;2-3.
A case of a vagal body tumor with a solitary cervical node metastasis is described. There was a remarkable familial association: a biopsy-proven paraganglioma occurred in two members of the patient's family and there was a strong clinical suspicion of a paraganglioma in two others. In a review of the literature, eight patients with metastasizing vagal body tumors and eight patients in whom the vagal body tumor was a component of multicentric presentation of paragangliomas were found. Only one other patient in whom there was a familial occurrence involving a vagal body tumor has been reported. Ultrastructural study of the cervical node metastasis revealed the presence of light and dark chief cells containing scanty, membrane-bound, densecore, neurosecretory-type granules. Atypical granules were noted in a few of the dark cells. Nerve fibers, synaptic vesicles, and sustentacular cells, such as occur in normal paraganglionic tissue, were not observed in this tumor.
本文描述了一例伴有孤立性颈部淋巴结转移的迷走神经体瘤病例。该病例存在显著的家族关联:患者家族中有两名成员经活检证实患有副神经节瘤,另有两名成员临床上高度怀疑患有副神经节瘤。在文献回顾中,发现了8例伴有转移的迷走神经体瘤患者以及8例迷走神经体瘤为副神经节瘤多中心表现一部分的患者。仅另有1例报道的家族性迷走神经体瘤患者。对颈部淋巴结转移灶的超微结构研究显示,存在浅色和深色主细胞,这些细胞含有少量、膜结合、致密核心、神经分泌型颗粒。在少数深色细胞中发现了非典型颗粒。在该肿瘤中未观察到正常副神经节组织中存在的神经纤维、突触小泡和支持细胞。