Rodriguez Fausto J, Scheithauer Bernd W, Fourney Daryl R, Robinson Christopher A
Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, SW, Rochester, MN 55905, USA.
Acta Neuropathol. 2008 Mar;115(3):363-6. doi: 10.1007/s00401-007-0286-6. Epub 2007 Aug 31.
The so-called "calcifying pseudoneoplasm of the neural axis" is a rare tumefactive lesion presumed to be reactive in nature. To our knowledge, association with a true neoplasm has not been previously reported. We recently encountered the case of a 67-year-old woman who underwent resection of an incidentally discovered cerebellar cystic mass with a distinct, calcified component. Histology demonstrated a partially ossified, lobulated, chondrocalcific lesion surrounded by chronic inflammation, spindle to epithelioid cells, and occasional multinucleated giant cells-all features of calcifying pseudoneoplasm of the neural axis. A low-grade ependymoma associated with marked piloid gliosis was found contiguous to the lesion. The unique combination of an ependymoma with marked reactive gliosis and a calcifying pseudoneoplasm supports the reactive nature of the latter.
所谓的“神经轴钙化性假肿瘤”是一种罕见的瘤样病变,推测本质上是反应性的。据我们所知,此前尚未报道过与真正肿瘤相关的情况。我们最近遇到一例67岁女性,她接受了手术切除偶然发现的小脑囊性肿块,该肿块有一个明显的钙化成分。组织学显示为部分骨化、分叶状、软骨钙化性病变,周围有慢性炎症、梭形至上皮样细胞,以及偶尔的多核巨细胞——这些都是神经轴钙化性假肿瘤的特征。在该病变相邻处发现了一个与明显的毛细胞型胶质增生相关的低级别室管膜瘤。室管膜瘤与明显的反应性胶质增生以及钙化性假肿瘤的独特组合支持了后者的反应性本质。