González-Cámpora R, Otal-Salaverri C, Panea-Flores P, Lerma-Puertas E, Galera-Davidson H
Department of Pathology, University of Seville, Spain.
Acta Cytol. 1988 May-Jun;32(3):386-90.
A comparative study of six paragangliomas from different locations and with different clinical behavior was performed. The fine needle aspirates in all cases were similar: abundant cells with round or oval nuclei and marked anisokaryosis with a tendency to form acini or follicular structures. Pheochromocytomas often contained binucleated cells and had cells with prominent intranuclear cytoplasmic inclusions more often than did other paraganglionic tumors. Similar features were seen in the excised tumors. Evaluation of the significance of nuclear variations with morphometry confirmed the subjective impression that nuclear pleomorphism is not an indicator of the biologic behavior of these lesions; paradoxically, malignant paragangliomas show less anisokaryosis than do their benign counterparts.
对来自不同部位且具有不同临床行为的6例副神经节瘤进行了一项比较研究。所有病例的细针穿刺抽吸物相似:细胞丰富,细胞核呈圆形或椭圆形,核大小明显不等,有形成腺泡或滤泡结构的倾向。嗜铬细胞瘤常含有双核细胞,与其他副神经节瘤相比,其细胞核内有明显的胞质内包涵体的细胞更为常见。在切除的肿瘤中也观察到类似特征。通过形态计量学评估核变异的意义,证实了核多形性并非这些病变生物学行为指标的主观印象;矛盾的是,恶性副神经节瘤的核大小不等比良性副神经节瘤少。