P. Robbins et al., CENTRAL NEUROCYTOMA - A CLINICOPATHOLOGICAL, IMMUNOHISTOCHEMICAL AND ULTRASTRUCTURAL-STUDY OF 7 CASES, Pathology research and practice, 191(2), 1995, pp. 100-111
Characterised by distinctive clinicopathological features, the central
neurocytoma (CN) is an uncommon and possibly under-recognised primary
cerebral neuronal neoplasm. We present clinical and pathological deta
ils of seven patients with CN. Histological examination revealed a gre
ater diversity of morphological appearances than is typically describe
d in CN. No anaplastic features were identified. Cellular areas resemb
ling both oligodendroglioma and ependymoma were present in all cases,
but each tumour also contained stroma rich areas with hyalinised or an
eurysmal vessels. Synaptophysin was expressed by all tumours and proba
bly represents the immunohistochemical marker of choice for identifyin
g CN. Distinguishing ultrastructural features included rounded cell bo
dies separated by numerous cell processes containing microtubules, ple
omorphic neurosecretory granules and occasional synapses. Ki-67 immuno
staining revealed a low cell proliferation index in each case. The dis
tinction of CN from other pathological mimics can be reliably made usi
ng this multiparametric approach to diagnosis. The generally benign be
haviour of CN is confirmed, though there was one patient death in the
follow-up period of 10-122 months. Aggressive behaviour in this case w
as not associated with anaplastic histological features.